Introduction: Evidence-Based Practice for Major Depressive Disorder

Major Depressive Disorder: Definition, Epidemiology, and Course


The Diagnostic and Statistical Manual of Mental Disorders (4th edition—DSM-IV) defines Major Depressive Disorder (MDD) as the presence of five (or more) of the following nine symptoms during the same 2-week period:



1. Depressed mood most of the day, nearly every day.


2. Markedly diminished interest or pleasure in almost all activities (anhedonia).


3. Significant weight loss/gain or decrease/increase in appetite.


4. Insomnia or hypersomnia.


5. Psychomotor retardation or agitation.


6. Fatigue or loss of energy.


7. Feelings of worthlessness (or excessive or inappropriate guilt).


8. Diminished ability to concentrate or make decisions.


9. Recurrent thoughts of death.


Symptoms must be present most of the day, nearly every day, and should represent a significant change from previous functioning. Importantly, one of the nine symptoms has to be either depressed mood or anhedonia. In adolescents or children, irritable mood can be substituted for depressed mood. Less than 5% of depressed adolescents typically endorse anhedonia (Rohde, Beevers, Stice, & O’Neil, 2009), so depressed or irritable mood tends to be the hallmark symptom of adolecent depression. Significant weight loss or gain is typically defined as 5% or more change in body weight in a month when not dieting. These symptoms must cause significant distress or impairment in social, occupational, or other important areas of functioning. Finally, these symptoms should not be attributable to substances (e.g., drug abuse, medication changes), medical conditions (e.g., hypothyroidism), or the death of a loved one.


Recent epidemiological research indicates that the 12-month prevalence rates for MDD was 6.6% (95% CI, 5.9%–7.3%) among adults residing in the United States. Lifetime prevalence for MDD was 16.2% (95% CI, 15.1%–17.3%). Put differently, approximately 13.5 million adults experienced MDD in the past year, and 34 million adults have experienced MDD at some point in their lives. Approximately 51% who experienced MDD in the past year received health-care treatment for MDD, although treatment was considered adequate in only 21% of the cases (Kessler, Berglund et al., 2003). Thus, MDD is a prevalent and pervasive mental health disorder that is unfortunately not treated optimally in the United States.


Obtaining adequate treatment is important, as the course of MDD tends to be relatively prolonged. One of the largest studies of MDD recovery among individuals seeking treatment found that 50% of the sample recovered from MDD by 6 months, 70% within 12 months, and 81% within 24 months. Approximately 17% did not recover within the 5-year follow-up period (Keller et al., 1992). The first 6 months represents a particularly important time period for MDD recovery, as the rate of MDD recovery significantly slows after 6 months. Similarly, Kessler (2009) writes that time to recovery of MDD in nontreatment-seeking populations “appears to be highly variable, although epidemiological evidence is slim” (p. 29). One study found that 40% had recovered from MDD by 5 weeks and 90% had recovered within 12 months (McLeod, Kessler, & Landis, 1992). Another study reported that mean time to recovery was 4 months and that approximately 90% had recovered by 12 months (Kendler, Walters, & Kessler, 1997). Taken together, these data suggest that most participants from a community sample recover from MDD within 12 months.


Risk for MDD is especially pronounced during adolescence (Blazer, Kessler, McGonagle, & Swartz, 1994; Lewinsohn, Hops, Roberts, & Seeley, 1993). Prevalence rates range from 10% to 18.5% (Kessler & Walters, 1998). This is especially true for adolescent girls, who are approximately twice as likely to experience depression as adolescent boys (Hankin et al., 1998). Longitudinal studies show that increases in MDD prevalence for women occur at approximately 15 years of age and persist into adulthood (Hankin et al., 1998; Kessler, Berglund et al., 2003; Lewinsohn, Hops et al., 1993; Nolen Hoeksema & Girgus, 1994; Prinstein, Borelli, Cheah, Simon, & Aikins, 2005).


Treatment for adolescents with subthreshold symptoms of MDD may be particularly important, as adolescents with elevated symptoms (but who do not meet criteria for MDD) are at high risk for future onset of MDD. Lewinsohn, Roberts, and colleagues et al. (1994) found that elevated depressive symptoms was one of the most potent risk factors for future MDD onset over the subsequent year out of dozens of risk factors. Seeley, Stice, and Rohde (2009) recently examined a broad array of putative risk factors (e.g., parental support, negative life events, depressive and bulimic symptoms, substance use, attributional style, body dissatisfaction, physical activity, social adjustment, delinquency) for MDD onset in a longitudinal study of 496 adolescent girls 15 to 18 years old. Among 18 variables tested, the strongest predictor of future MDD onset was subthreshold depressive symptoms. Girls with elevated symptoms were at approximately five times greater risk for future MDD onset than girls with low symptoms (28% versus 6%).


Unfortunately, treatment utilization among depressed adolescents is also lacking. Approximately 60% of adolescent with MDD receive treatment (Lewinsohn, Rohde, & Seeley, 1998). Individual outpatient psychotherapy administered by a mental health provider is the most common form of treatment. Adolescents with more severe depression, a comorbid condition, a past history of MDD, a history of suicidal attempts, and academic problems, and females were more likely to receive treatment. However, those who had received treatment were not less likely to relapse into another episode of depression during young adulthood (Lewinsohn et al., 1998). This suggests that the typical treatment received by depressed adolescents may not have been effective at changing the underlying cause of depression onset.


Assessment of Depression


A number of questionnaires and diagnostic interviews are available to assess depression symptoms and MDD in adolescents and adults. We review these assessments for adults and adolescents separately.


Adults


The Structured Clinical Interview for DSM-IV Axis I Disorders (SCID) diagnoses is the most common method for determining whether an adult meets criteria for MDD (and many other DSM-IV diagnoses). This is a semistructured interview that inquires about current and past symptoms. Length of an SCID interview can be quite variable—individuals with no past or current symptoms can complete the interview in about 15 minutes. Individuals with more complex symptom presentations can take several hours to complete a SCID interview. A typical SCID interview takes about 90 minutes. With adequate interviewer training, the SCID interview has excellent reliability and has been used extensively in depression research. Determining the validity of the SCID is more complex, as it is typically used as the gold standard to determine a diagnosis. Nevertheless, there is ample evidence that an SCID diagnosis converges with diagnoses derived from other diagnostic interviews (First, Spitzer, Williams, & Gibbon, 1995). For more detail on the SCID, see http://www.scid4.org/.


The World Health Organization (WHO) Composite International Diagnostic Interview (CIDI) is a psychiatric diagnostic interview designed to be administered by nonclinicians. The CIDI assesses for most Axis I disorders (including MDD) as defined by the DSM-IV and the ICD-10. It also assesses service use, use of medications, and barriers to treatment. There is substantial evidence for the reliability and validity of the CIDI. It has been translated into numerous languages and is typically used in large-scale epidemiological studies (Kessler, Berglund et al., 2003). For more information, see http://www.hcp.med.harvard.edu/wmhcidi/index.php.


The Mini-International Neuropsychiatric Interview (MINI) is another diagnostic interview that was developed jointly by psychiatrists and clinicians in the United States and Europe (Sheehan et al., 1998). It is much briefer than the SCID and CIDI, with an administration time of approximately 20 minutes. It assesses 15 of the most common DSM-IV Axis I disorders, including current and past history of MDD. Due to its brevity, it is often used as a screening interview that is subsequently confirmed with a subsequent in-depth diagnostic interview. It also has excellent reliability and validity (Sheehan et al., 1997). For more information, see https://www.medical-outcomes.com/index.php.


A number of self-report and interviewer-based assessments of depression severity are also available. The most commonly used interview-based depression severity assessments with adults include the Hamilton Rating Scale for Depression (HAM-D) and the Inventory of Depressive Symptomatology (IDS). The 17-item HAM-D was originally developed in 1960 and subsequently revised a number of times (Hamilton, 1960). It has been used primarily in antidepressant medication trials. The HAM-D has been criticized on the basis that it has poor content validity (may overemphasize somatic symptoms, which are especially responsive to antidepressant medication treatment), having a nonoptimal response format for many items, several items do not appear to discriminate people at high and low ends of the depression continuum, and other psychometric flaws (Bagby, Ryder, Schuller, & Marshall, 2004).


As a result, a newer interview-based assessment of depression severity, the IDS, is gaining popularity (Rush, Thomas, & Paul-Egbert, 2000). The 30-item IDS (and the 16-item Quick IDS) assess the severity of depression symptoms in the past seven days. The items measure all DSM-IV symptoms of MDD, although a total score is typically used to assess depression severity. There is much evidence to suggest that the IDS has good psychometric properties, including good internal reliability, test-retest reliability and adequate content, criterion, and construct validity (e.g., Rush et al., 2003). The IDS has been translated into more than 20 different languages and is used widely in medical research. Items can be added to the IDS to facilitate computation of the HAM-D total score within the IDS interview. Further, there is also a self-report version of the IDS to be completed by patients. The IDS (and its corresponding short and self-report versions) are available for download at http://www.ids-qids.org/index.html.


There are also a number of other excellent self-report assessments of depression severity. The Beck Depression Inventory-II (BDI-II) is a 21-item self-report questionnaire that is among the most commonly used instrument to assess depression severity (Beck, Steer, & Brown, 1996). It is often used in research involving psychological treatments. The BDI-II has demonstrated adequate internal consistency, test-retest reliability, and construct validity (Dozois, Dobson, & Ahnberg, 1998). A score of 12 or less is considered nondepressed, whereas a score of 20 or greater typically indicates moderate or greater depression severity (Dozois et al., 1998). To obtain the BDI-II, see http://www.pearsonassessments.com/HAIWEB/Cultures/en-us/Productdetail.htm?Pid=015–8018–370&Mode=summary.


Alternatively, the Center for Epidemiologic Studies—Depression (CESD) is another common assessment of depression severity (Radloff, 1977). The CESD was developed to be a brief self-report scale designed to measure depression severity in the general (nonpsychiatric) population. It has 16 items that measure the severity of depression symptoms in the past week. It has very good internal consistency and test-retest reliability. Validity was established by correlating the CESD with other depression inventories and clinical ratings of depression (Radloff, 1977). A 10-item version has also been developed (Irwin, Artin, & Oxman, 1999). It is a widely used depression scale, particularly when the majority of the sample is expected to be currently depressed.


Adolescents


The Kiddie-Sads-Present and Lifetime version (K-SADS-PL) is a semistructured diagnostic interview designed to assess severity ratings of symptomatology as well as current and past episodes of psychopathology in adolescents according to DSM-IV criteria (Kaufman et al., 1997). The full interview assesses more than 35 mental health diagnoses, including MDD. The K-SADS-PL is administered to parents and the adolescent. Other sources of information may also be incorporated (e.g., school reports) into a summary rating. It is typically recommended to start the interview with the adolescent first, followed by the parents. Clinical judgment is required when there are discrepancies in the content of the reports from adolescents and parents. The K-SADS has been found to have acceptable test-retest reliability (k’s = .60–1.00), inter-rater reliability (k’s = .60 –1.00), and internal consistency (alpha’s = .68–.84) for MDD ratings, and to discriminate between disordered and nondisordered adolescents (Ambrosini, 2000; Kaufman et al., 1997; Lewinsohn et al., 1993). For more information, see http://www.wpic.pitt.edu/ksads/default.htm.


The Children’s Depression Inventory is a 27-item, self-report assessment of depression severity that was developed for children and adolescents between the ages of 7 and 17 years (Kovacs, 1992). Each item describes a symptom, and the adolescent rates the severity of each symptom over the past two weeks on a 3-point scale. A 10-item version is also available. The normative sample was ethnically and geographically diverse. Internal consistency and test-retest reliability are excellent. There are five subscales (negative mood, interpersonal difficulties, negative self-esteem, ineffectiveness, and anhedonia), although using the CDI total score is the most common approach to assessing symptom severity. For more information on the CDI, see http://www.pearsonassessments.com/pai/.


Evidence-Based Treatment for Depression: Interventions Not Included in This Volume


There are a number of treatments for depression that have empirical support indicating that the treatment is effective for the treatment of depression. Of course, we preferred to include an in-depth review of each and every one of these treatments in this book. However, this was not practical or feasible. Instead we selected a variety of treatments that have a solid research base, and each chapter provides an in-depth description of a treatment. Rather than inadvertently convey that these are the only effective treatments for depression, we now provide a brief overview of other treatments that have a solid research base that are not included, for one reason or another, in this text.


Pharmacological Treatments


Several classes of medications are used to treat depression. Three basic types of antidepressant medications include tricyclic antidepressants, monoamine oxidase inhibitors (MAOIs), and serotonin-specific reuptake inhibitors (SSRIs). There are some newer antidepressant medications that do not fit neatly into these categories because they have different mechanisms of action (e.g., venlafaxine and nefazedone). The efficacy rates for these newer antidepressant treatments are comparable to the efficacy rates of SSRIs (Stahl, Entsuah, & Rudolph, 2002).


Tricyclic Medications


Prior to the introduction of SSRIs, tricyclic medications were the most commonly prescribed antidepressant medications. Although the exact mechanism of action is not completely understood, tricyclic medications reduce the transmission of norepinephrine by blocking its reuptake and allowing for norepinephrine to pool in the synapse. This leads to decreased production of norepinephrine (i.e., downregulation). These medications can take two to eight weeks before a therapeutic effect occurs, which may be due to neurogenesis (nerve growth) in the hippocampus (Santarelli et al., 2003). Tricyclic mediations can produce a number of side effects including blurred vision, dry mouth, constipation, drowsiness, and weight gain. As a result, 40% of patients stop taking these medications, even though with careful management these side effects can disappear. Tricyclic medications improve depression symptoms in approximately 50% of patients; if we exclude patients who stopped taking the medication, improvement rates climb to 70% (Depression Guideline Panel, 1993). Taking excessive doses of these medications can be lethal, so individuals with suicidal tendencies should be monitored closely.


MAOIs


These antidepressant medications block the enzyme MAO, which degrades neurotransmitters such as serotonin and norepinephrine. As a result, more of these neurotransmitters are available in the synapse, leading to downregulation. MAOIs appear to be as effective as tricyclic medications and have fewer overall side effects (Depression Guideline Panel, 1993). However, people prescribed MAOIs have significant food restrictions. They cannot consume food or drinks that contain tyramine, such as cheese, red wine, or beer. Doing so can lead to significant increases in blood pressure that in some cases can be fatal. MAOIs can also interact with other commonly used drugs, such as cold medicine. As a result, MAOIs are not often prescribed.


SSRIs


SSRIs are the most commonly prescribed class of antidepressant medication and are generally considered the first choice for antidepressant treatment. These medications block the reuptake of presynaptic serotonin, leaving more available at the receptor site. This facilitates increased serotonin production over time. Although this class of drugs is relatively new, the efficacy of SSRIs is comparable to MAOI and tricyclic medications. Approximately 50% experience symptom improvement, but depression fully remits in only about 25% to 30% of patients (Trivedi et al., 2006). SSRIs have fewer side effects than the other antidepressant medications, thus accounting for their popularity despite similar efficacy compared to older treatments. Most common side effects include physical agitation, sexual dysfunction, low sexual desire, and sleep difficulties.


Placebo Response


Although antidepressant medication treatment is a common and accepted form of treatment for depression, there is some controversy about whether it is more effective than pill placebo (Moncrieff & Kirsch, 2005). That is, do antidepressant medications improve symptoms beyond the effect of believing that medication treatment will be effective? A recent study addressed this question using meta-analysis of six studies that compared antidepressant medication to pill placebo (Fournier et al., 2010). In short, this study found that antidepressant treatment was only mildly more effective than placebo for people with relatively low symptoms of depression, whereas a clinically significant benefit of antidepressant medication compared to placebo was observed for patients with more severe forms of depression. Thus, medication treatment may be particularly beneficial for individuals with more severe forms of the disorder. However, this study was based on only six studies (718 patients) involving two antidepressant medications (paroxetine and imipramine), so much more work needs to be done in this area.


Antidepressant Treatment With Adolescents


Far less is known about the treatment efficacy of antidepressant medication in adolescents. A recent meta-analysis indicated that antidepressant treatment appears to be effective for adolescents (Bridge et al., 2007). Across 13 clinical trials and 2910 participants 7 to 17 years old, overall response to treatment was 61%, compared to 50% for placebo. Adolescents had a better response to antidepressant treatment relative to placebo than children, but this was due to a stronger placebo response in children. Overall response rate to antidepressant treatment (not accounting for differences in placebo response) for adolescents and children was very similar (62% versus 65%). The efficacy of antidepressant treatment was inversely related to the duration of depressive disorder. This suggests that providing adolescents treatment earlier in the course of the depressive episode may be beneficial. Fluoxetine (Prozac) is currently the only medication approved by the U.S. Food and Drug Administration (FDA) for the treatment of depression in children and adolescents (ages 8 and older).


Recently, there has been some concern that antidepressant medications may increase risk for suicidal ideation and behavior among a subset of adolescents. The FDA reviewed placebo-controlled clinical trials of SSRIs involving 2,200 youth and found that risk for suicidal thinking or behavior was double among those receiving SSRIs versus placebo, although base rates for suicidal behavior were relatively low (4% versus 2%). In response, the FDA adopted a serious “black box” label warning, indicating SSRIs could increase the risk of suicidality in youth. The FDA also recommended especially close monitoring in the first four weeks of SSRI treatment, a time period when suicidal ideation and behavior were most likely to occur. Interestingly, epidemiological research indicates that increased SSRI prescriptions are associated with lower rates of completed suicide in adolescents and children (Gibbons, Hur, Bhaumik, & Mann, 2006). Further, after instituting a “black box” warning, prescriptions for SSRIs decreased and rates of completed suicide subsequently increased among children and adolescents (Gibbons et al., 2007). Thus, this is a highly contentious issue, with conflicting evidence about whether SSRIs contribute to or prevent suicidal behavior.


Psychological Treatments


In this section, we review interpersonal psychotherapy, marital therapy, family treatment, and psychological treatment with adolescents.


Interpersonal Psychotherapy (IPT)


There is substantial evidence that IPT is an effective treatment for depression. It is generally recommended as an acute treatment for adult depression by numerous guidelines and panels (e.g., Depression Guideline Panel, 1993). IPT has been shown to be equally effective as acute antidepressant treatment with amitriptyline for the reduction of depression symptoms, and combined treatment (IPT + amitriptyline) was more effective than either treatment alone (Weissman et al., 1979). Further, a large multisite study has demonstrated that IPT is equally effective as antidepressant treatment with imipramine and CBT for the treatment of mild depression and that IPT demonstrated a slight advantage over CBT for the treatment of more severe forms of depression (Elkin et al., 1989).


The IPT treatment manual has been translated into numerous languages and implemented around the world. Later we provide a brief overview of the concepts and techniques of IPT. For more detail, treatment manuals are available for IPT with depressed adults (Weissman, Markowitz, & Klerman, 2000), depressed adolescents (Mufson, Moreau, Weissman, & Klerman, 1993), and for delivery in group formats (Wilfley, MacKenzie, Welch, Ayres, & Weissman, 2000).


IPT is based on the notion that life events influence the onset and expression of depression. The main goal of IPT is to help the patient better understand and cope with depression by making connections between current life events and the onset of symptoms. This is achieved in part by helping patients to overcome interpersonal problems in an effort to improve life circumstances and relieve depression. Its focus is on current events and relationships, rather than on past relationships or problems. IPT techniques include (a) an opening question: patients provide information regarding their current mood state and events that contributed to the current mood; (b) communication analysis: patients review an important affectively charged life event; (c) exploration of patient’s wishes and options: patients review desired outcomes for the situations described in session; (d) decision analysis: patients decide which options to use in future life situations, and (e) role playing: patients practice implementing new strategies and solutions to interpersonal problems.


Treatment with IPT typically lasts 12 to 16 weeks when implemented in clinical trials, although longer versions of IPT have been developed (Klerman, DiMascio, Weissman, Prusoff, & Paykel, 1974). The early phase of treatment involves a diagnostic evaluation, presentation of the IPT framework, and a review of the patient’s psychiatric history. Reviewing key interpersonal relationships is a major focus of this phase. The therapist also identifies life difficulties that contribute to the patient’s depressive symptoms in one of four key areas: (1) grief, (2) role disputes, (3) role transitions, and (4) interpersonal deficits. The middle phase of treatment focuses on remediating these problem areas. For instance, if the main issue is the patient’s difficulty with social skills, much of the treatment will be focused on improving those skills (e.g., via role plays with the therapist). The final phase of treatment helps the patient to consolidate the gains, identify potential weaknesses, and develop a plan to cope with increases in depression should they occur again.


Marital Therapy


Although there is good evidence that marital therapy can be used to successfully treat marital discord (Beach, Jones, & Franklin, 2009), there is emerging evidence that martial therapy can effectively treat depression. Three studies found that behavioral marital therapy was equally effective for treating depression as cognitive therapy, and both were superior to a waitlist control (Beach & O’Leary, 1992; Emanuels-Zuurveen & Emmelkamp, 1996; Jacobson, Dobson, Fruzzetti, Schmaling, & Salusky, 1991). Behavioral martial therapy had the additional benefit of reducing marital discord to a greater extent than cognitive therapy. Other forms of marital treatment have been shown to be effective, such as spouse-aided cognitive therapy (Emanuels-Zuurveen & Emmelkamp, 1997), cognitive marital therapy (Teichman, Bar-El, Shor, & Sirota, 1995), and IPT modified for couples (Markowitz, Weissman, & Gabbard, 2009), although the evidence base is somewhat smaller for these forms of treatment.


Given the success of Behavioral Marital Therapy (BMT) for the treatment of depression, we provide a brief review of this intervention (for a more thorough review, see Beach et al., 2009). BMT is a relatively brief time-limited (approximately 10 weeks) treatment that is indicated for couples when one partner is depressed and marital discord is present. Initially, therapists identify relationship stressors and develop a plan to eliminate them, while simultaneously increasing the number of positive interactions between the couple. Ideally, this phase of treatment will improve depressed mood and prepare the couple for the second phase of treatment aimed at restructuring the marital relationship. The main focus of this second phase of treatment is to improve communication between partners, engage in more productive and healthy problem solving, and improve day-to-day interactions between the couple. Most of the work in BMT occurs during this phase. The final phase of treatment involves preparation for termination from treatment and setting a plan to cope with future stressors that may increase vulnerability to depression and marital discord.


Family Treatment


Family-based treatment is another type of intervention that appears to be effective for depression. For instance, severely depressed patients who received family treatment were more likely to improve and report less suicidal ideation than patients who did not receive family treatment (Miller et al., 2005). Although there are a number of family-based treatments, the McMaster approach appears to be effective for treating adult depression (Miller, Ryan, Keitner, Bishop, & Epstein, 2000).


This treatment takes a systems approach to understanding dysfunction within the family. It assumes that: (a) all parts of the family are interrelated; (b) one member of the family cannot be fully understood in isolation from the rest of the family; and (c) family structure, organization, and interactions influence family members’ behavior. At the beginning stages of treatment, family functioning is evaluated in six domains: problem-solving, communication, roles, affective responsiveness, affective involvement, and behavior control. The family and the therapist then develop a contract, which identifies the expectations, goals, and commitments regarding treatment. Treatment is then initiated to mitigate identified problems. Treatment focuses on behavioral changes via task setting that occurs between sessions. Subsequent sessions then focus on evaluating the success of those assignments and then planning future tasks that build on prior successes. A number of techniques are also explored during the session to help improve the family’s ability to communicate and change the problems without the help of the therapist. The final stages of treatment focus on summarizing treatment, setting long-term goals, and determining whether future follow-up treatment is necessary. For more detail, see Epstein, Bishop, Miller, and Keitner (1988).


Psychological Treatment With Adolescents


Although CBT treatment has the most empirical support for the psychological treatment of adolescent depression (see Appendix A), evidence is accumulating for other forms of treatment. For instance, two studies have documented the efficacy of adolescent IPT (IPT-A) for depressed adolescents versus brief supportive therapy (Mufson, Weissman, Moreau, & Garfinkel, 1999) and waitlist (Rosselló & Bernal, 1999). Further, in a study involving training community clinicians to deliver the intervention, IPT-A outperformed treatment as usual (Mufson et al., 2004), with 50% recovering from depression in IPT-A versus 34% in treatment as usual. Adolescents receiving IPT-A also reported significantly better improvement in overall functioning and social functioning at the end of treatment than those who received treatment as usual. Thus, IPT-A is considered an efficacious treatment for adolescent depression (David-Ferdon & Kaslow, 2008).


Family-oriented treatment also appears to be an efficacious treatment for adolescent depression. One of the first studies compared systemic behavior family therapy (SBFT) to CBT and supportive therapy for the treatment of depression. SBFT identifies the presenting problems within the family and then focuses on changing dysfunctional interaction patterns and improving communication within the family. At the end of acute treatment (12 to 16 sessions), 17% of CBT participants, 32% of SBFT participants, and 42% of the supportive treatment participants still met criteria for MDD. However, by the 2-year follow-up, more than 80% had recovered from MDD and treatment did not predict who was more likely to recover. Thus, although this literature is sparse and much more work is needed, family treatment may work less efficiently than CBT for treating adolescent depression, but longer-term outcomes appear to be comparable.


Combined Pharmacological and Psychological Treatment


Given that pharmacological and psychological treatments can be effective in isolation, a related question is whether combining these treatments can improve depression treatment outcomes further. A number of studies have examined this question, including several meta-analyses. One meta-analysis found that adding psychotherapy to antidepressant treatment almost doubled the response rate compared to antidepressant treatment alone (Pampallona, Bollini, Tibaldi, Kupelnick, & Munizza, 2004). Participants in the combined treatment were also less likely to drop out of treatment compared to those who only received medication.


However, the picture is less clear when examining the impact of adding pharmacotherapy to psychotherapy. One review found that combined treatment was not more effective than psychotherapy for less severe forms of depression, but a significant advantage was observed for combined treatment for more severe recurrent depressions (Thase et al., 1997). Yet another review indicates that combined treatment compared to single treatment leads to small improvements in depression (Friedman et al., 2004). Overall, combined treatment in adults may be beneficial; however, the effects tend to be modest and are probably best indicated for more severe forms of depression.


Relatively fewer studies have examined the efficacy of combined treatment in adolescents. The Treatment for Adolescents with Depression Study (TADS) is a large multisite clinical research study examining the effectiveness of antidepressant medication, CBT psychotherapy, and their combination among adolescents 12 to 17 years old (Treatment for Adolescents with Depression Study Team, 2003). This study was conducted at 13 clinics across the United States (at a cost of $17 million) and involved 439 adolescents. After 12 weeks of treatment, 71% receiving combined treatment, 61% receiving fluoxetine (Prozac), 44% receiving CBT, and 35% receiving pill placebo were much or very much improved (Treatment for Adolescents with Depression Study Team, 2004). After 18 weeks of treatment, results were similar, as combination treatment was still most effective. By 36 weeks, the response rate was highest for combination treatment (86%), but response rates for fluoxetine and CBT had caught up (81% each)(Treatment for Adolescents with Depression Study Team, 2007). Interestingly, rates of suicidal thinking or behavior were highest in fluoxetine only (15%), compared to combined treatment (8%) and CBT alone (6%). Given adolescents’ rapid responses to combined treatment, these data suggest combining CBT with fluoxetine may be the quickest, most effective, and safest treatment for adolescent depression.


Evidence-Based Treatment for Depression: Interventions Included in This Volume


This book includes six chapters. In this chapter we provide background information about how depression is defined and measured. We also review effective treatments for adolescent and adult depression that are not included in this volume. In the remainder of this chapter, we provide a preview of interventions that are included in the subsequent chapters.


In Chapter 2, Paul Rohde reviews Cognitive Behavioral Treatment (CBT) for use with adolescents. He describes a group-based treatment for adolescent depression based on the Adolescent Coping With Depression (CWD-A) course. This course has outstanding empirical evidence for its efficacy, which is reviewed in Appendix A. Dr. Rohde also describes individual CBT treatment for depressed adolescents. The approach is consistent with treatment provided in the Treatment for Adolescent Depression Study (TADS). Incidentally, Dr. Rohde is a member of the Treatment for Adolescent Depression Study team, and he helped implement the CBT intervention in TADS. This chapter reviews the general structure of CBT sessions and provides an in-depth review of core CBT skills, such as goal setting, behavioral activation, and countering cognitive distortions. He then reviews optional CBT skills, such as problem solving, social skills, and relaxation. These can be implemented based on the adolescents’ needs and duration of treatment. Throughout the chapter, Dr. Rohde uses case examples to illustrate his points.


In Chapter 3, Cory Newman reviews the application of CBT to adult depression. Before reviewing the CBT mechanics, he provides an excellent review of commonly held myths about CBT and succinctly describes why each is, indeed, a myth. For instance, he debunks the notion that CBT has to be short-term, that the therapeutic relationship does not matter in CBT, and that CBT is simply replacing negative thoughts with the power of positive thinking. Next, he reviews how to conceptualize depression from a CBT perspective and provides two illuminating case examples. He then reviews the core techniques used in CBT when treating depressed adults. Note that there is some overlap with techniques discussed in Chapter 2; however, you will see a number of unique approaches as well. For instance, in addition to reviewing activity scheduling and responding to negative thoughts, he also reviews how to incorporate role-play, homework, and behavioral experiments. He also reviews how to apply CBT to suicidal clients—suicidal ideation and behavior is a common symptom of depression and Dr. Newman provides excellent advice on how to treat suicidal clients from a CBT perspective. Finally, he concludes with a review of additional issues that arise during CBT for depression, such as how to identify the client’s strengths, what to do when a depressed person takes on a “depressive identity,” or how to work with hopelessness. Together, Chapters 2 and 3 provide an in-depth review of CBT for depression and also discuss clinical issues that often arise during treatment but are often not addressed in treatment manuals or the research literature.


Although the research support for CBT for depression is impressive, the question was raised whether behavioral activation (BA) alone would be sufficient for the treatment of depression. A pioneering dismantling study compared the efficacy of BA versus CBT, with very encouraging results for BA (Jacobson et al., 1996). As a result of that study, BA treatment was developed and it is now an empirically supported treatment. In Chapter 4, Jonathan Kanter, William Bowe, David Baruch, and Andrew Busch review a variant of BA that includes the core features of the BA treatments that have been developed. They provide a rich overview of the theory behind BA and its general principles. They discuss how to convey the BA rationale to clients and how to deal with clients’ reactions to the conceptualization. Activity scheduling is a hallmark technique of BA. Thus, much of Chapter 4 is devoted to reviewing this technique in detail. They also incorporate a review of clients’ values—this approach is used to help make behavioral activation more meaningful. Ideally, clients are working toward goals that are personally meaningful and are consistent with their own values. The inclusion of values is a recent and cutting-edge addition to BA. They also review common barriers to treatment success, such as avoidance and failure to complete homework assignments. This chapter includes a number of detailed case descriptions, which help to illustrate this intervention. Although BA may sound straightforward, after reading this chapter, you will quickly see that this intervention is much more complex than the name implies.


Although depression is typically thought of as episodic, with periods of well-being interspersed with periods of depression, for some people depression takes a much more chronic course. Remission from MDD may be incomplete, or the MDD episode may persist for much longer than commonly expected. About 3% of the population suffers from this type of chronic depression (Kessler et al., 1994). Importantly, chronic forms of MDD are associated with impaired work performance, poorer social functioning (Wells, Burnam, Rogers, Hays, & Camp, 1992), increased health care utilization (Weissman, Leaf, Bruce, & Florio, 1988), and higher rates of attempted suicide (Klein et al., 1998) than are more acute forms of depression. Despite the large societal impact of chronic depression, until recently, few psychological treatments had been developed and shown to be effective for treating chronic depression.


In Chapter 5, James McCullough and Jennifer Penberthy describe the leading psychological treatment for chronic depression, Cognitive Behavioral Analysis System of Psychotherapy (CBASP). CBASP is one of the only treatments specifically developed for the treatment of chronic depression. In Chapter 5, the authors use a case study to illustrate the application of CBASP. They present a client who has been chronically depressed for approximately 2 years and then walk the reader through a course of CBASP treatment. They start with obtaining a psychiatric history, followed by collecting an interpersonal history. Next, a situational analysis is presented. This is a key CBASP intervention that involves reviewing past situations and identifying coping strategies employed in those situations. Over time, situational analysis helps clients to identify more effective ways of coping with stressors and increases their self-efficacy in those situations. Thus, CBASP shares many features of CBT, but also places much greater emphasis on interpersonal aspects of a client’s life.


In Chapter 6, Esteban Cardemil, Oswaldo Moreno, and Monica Sanchez tackle the tremendously important yet difficult issue of how to apply evidence-based practice to diverse populations. They correctly point out that much work on empirically supported treatments for depression has been conducted with people from European-American middle-class backgrounds. Thus, this raises the question of whether we need to adapt these interventions for other populations, and if so, how? Cardemil and colleagues propose that we should tailor interventions according to the needs of different populations. They provide several suggestions for how to adapt evidence-based treatments for diverse populations. This advice is based on empirical research with diverse populations, which is consistent with the philosophy of evidence-based practice. We believe this issue is critically important, as clients from diverse backgrounds who are seeking treatment are likely to become the norm rather than the exception.


We hope that after reading the various chapters in this volume you will have a better appreciation and understanding of evidence-based treatments for adolescents and adults with depression. Moreover, we hope that these descriptions inspire you to incorporate these techniques into your own practice or perhaps motivate you to receive additional training on one or more of the approaches reviewed in this volume. Ultimately, we hope you find this book to be of value for treating depressed clients. If you have feedback about any aspect of the book that you would like to share with us, do not hesitate to contact us at beevers@psy.utexas.edu or dwspringer@austin.utexas.edu.


References


Ambrosini, P. J. (2000). Historical development and present status of the Schedule for Affective Disorders and Schizophrenia for School-Age Children (K-SADS). Journal of the American Academy of Child and Adolescent Psychiatry, 39, 49.


Bagby, R. M., Ryder, A. G., Schuller, D. R., & Marshall, M. B. (2004). The Hamilton depression rating scale: Has the gold standard become a lead weight? American Journal of Psychiatry, 161, 2163–2177.


Beach, S. R. H., Jones, D. J., & Franklin, K. J. (2009). Marital, family, and interpersonal therapies for depression in adults. In I. H. Gotlib & C. L. Hammen (Eds.), Handbook of depression (2nd ed., pp. 624–641). New York, NY: Guilford Press.


Beach, S. R. H., & O’Leary, K. D. (1992). Treating depression in the context of marital discord: Outcome and predictors of response of marital therapy versus cognitive therapy. Behavior Therapy, 23, 507–528.


Beautrais, A. L., Joyce, P. R., Mulder, R. T., Fergusson, D. M., Deavoll, B. J., & Nightingale, S. K. (1996). Prevalence and comorbidity of mental disorders in persons making serious suicide attempts: A case-control study. American Journal of Psychiatry, 153, 1009–1014.


Beck, A. T., Steer, R., & Brown, G. K. (1996). Beck Depression Inventory (BDI-II). San Antonio, TX: Psychological Corp.


Blazer, D. G., Kessler, R. C., McGonagle, K. A., & Swartz, M. S. (1994). The prevalence and distribution of major depression in a national community sample: The National comorbidity survey. American Journal of Psychiatry, 151, 979–986.


Bridge, J. A., Iyengar, S., Salary, C. B., Barbe, R. P., Birmaher, B., Pincus, H. A.,…Ren, L. (2007). Clinical response and risk for reported suicidal ideation and suicide attempts in pediatric antidepressant treatment: A meta-analysis of randomized controlled trials. JAMA, 297, 1683–1696.


David-Ferdon, C., & Kaslow, N. J. (2008). Evidence-based psychosocial treatments for child and adolescent depression. Journal of Clinical Child and Adolescent Psychology, 37, 62–104.


Depression Guideline Panel. (1993). Clinical practice guideline: Depression in primary care. Rockville, MD: Department of Health and Human Services, Agency for Health Care Policy and Research.


Dozois, D. J. A., Dobson, K. S., & Ahnberg, J. L. (1998). A psychometric evaluation of the Beck Depression Inventory-II. Psychological Assessment, 10, 83–89.


Elkin, I., Shea, M. T., Watkins, J. T., Imber, S. D., Sotsky, S. M., Collins, J. F.,…. Glass, D.R. (1989). National Institute of Mental Health treatment of depression collaborative research program: General effectiveness of treatments. Archives of General Psychiatry, 46, 971–982.


Emanuels-Zuurveen, L., & Emmelkamp, P. M. G. (1996). Individual behavioural-cognitive therapy v. marital therapy for depression in maritally distressed couples. British Journal of Psychiatry, 169, 181–188.


Emanuels-Zuurveen, L., & Emmelkamp, P. M. G. (1997). Spouse-aided therapy with depressed patients. Behavior Modification, 21, 62–77.


Epstein, N. B., Bishop, D. S., Miller, I. W., & Keitner, G. I. (1988). Treatment manual—Problem centered systems therapy of the family. Providence, RI: Brown University Family Research Program.


First, M., Spitzer, R., Williams, J., & Gibbon, M. (1995). Structured clinical interview for DSM-IV—Patient version. New York, NY: Biometrics Research Department, New York State Psychiatric Institute.


Fournier, J. C., DeRubeis, R. J., Hollon, S. D., Dimidjian, S., Amsterdam, J. D., Shelton, R. C., et al. (2010). Antidepressant drug effects and depression severity: A patient-level meta-analysis. JAMA, 303, 47–53.


Friedman, M. A., Detweiler-Bedell, J. B., Leventhal, H. E., Home, R., Keitner, G. I., & Miller, I. W. (2004). Combined psychotherapy and pharmacotherapy for the treatment of major depressive disorder. Clinical Psychology: Science and Practice, 11, 47–68.


Gibbons, R. D., Brown, C. H., Hur, K., Marcus, S. M., Bhaumik, D. K., Erkens, J. A., et al. (2007). Early evidence on the effects of regulators’ suicidality warnings on SSRI prescriptions and suicide in children and adolescents. American Journal of Psychiatry, 164, 1356–1363.


Gibbons, R. D., Hur, K., Bhaumik, D. K., & Mann, J. J. (2006). The relationship between antidepressant prescription rates and rate of early adolescent suicide. American Journal of Psychiatry, 163, 1898–1904.


Greenberg, P. E., Stiglin, L. E., Finkelstein, S. N., & Berndt, E. R. (1993). The economic burden of depression in 1990. Journal of Clinical Psychiatry, 54, 405–418.


Hamilton, M. (1960). Development of a rating scale for depression. Journal of Neurology, Neurosurgery, and Psychiatry, 23, 56–62.


Hankin, B. L., Abramson, L. Y., Moffitt, T. E., Silva, P. A., McGee, R., & Angell, K. E. (1998). Development of depression from preadolescence to young adulthood: Emerging gender differences in a 10-year longitudinal study. Journal of Abnormal Psychology, 107, 128–140.


Irwin, M., Artin, K. H., & Oxman, M. N. (1999). Screening for depression in the older adult: Criterion validity of the 10-item center for epidemiological studies depression scale (CES-D). Archives of Internal Medicine, 159, 1701–1704.


Jacobson, N. S., Dobson, K., Fruzzetti, A. E., Schmaling, K. B., & Salusky, S. (1991). Marital therapy as a treatment for depression. Journal of Consulting and Clinical Psychology, 59, 547–557.


Jacobson, N. S., Dobson, K. S., Truax, P. A., Addis, M. E., Koerner, K., Gollan, J. K.,…Gortner, E. (1996). A component analysis of cognitive-behavioral treatment for depression. Journal of Consulting and Clinical Psychology, 64, 295–304.


Kaufman, J., Birmaher, B., Brent, D., Rao, U., Flynn, C., Moreci, P.,…Williamson, D. (1997). Schedule for affective disorders and schizophrenia for school-age children-present and lifetime version (K-SADS-PL): Initial reliability and validity data. Journal of the American Academy of Child and Adolescent Psychiatry, 36, 980–988.


Keller, M. B., Lavori, P. W., Mueller, T. I., Endicott, J., Coryell, W., Hirschfeld, R. M.,…Shea, T. (1992). Time to recovery, chronicity, and levels of psychopathology in major depression. A 5-year prospective follow-up of 431 subjects. Archives of General Psychiatry, 49, 809–816.


Kendler, K. S., Walters, E. E., & Kessler, R. C. (1997). The prediction of length of major depressive episodes: Results from an epidemiological sample of female twins. Psychological Medicine, 27, 107–117.


Kessler, R. C., & Wang, P. S. (2009). Epidemiology of depression. In I. H. Gotlib & C. L. Hammen (Eds.), Handbook of depression (2nd ed., pp. 5–22). New York, NY: Guilford.


Kessler, R. C., Berglund, P., Demler, O., Jin, R., Koretz, D., Merikangas, K. R., et al. (2003). The epidemiology of major depressive disorder. Results from the National Comorbidity Survey Replication (NCS-R). JAMA, 289, 3095–3105.


Kessler, R. C., McGonagle, K. A., Zhao, S., Nelson, C. B., Hughes, M., Eshleman, S.,…Wittchen, H. U. (1994). Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey.


Kessler, R. C., & Walters, E. E. (1998). Epidemiology of DSM-III-R major depression and minor depression among adolescents and young adults in the National Comorbidity Survey. Depress Anxiety, 7, 3–14.


Klein, D. N., Norden, K. A., Ferro, T., Leader, J. B., Kasch, K. L., Klein, L. M.,…. Schwartz, J. E. (1998). Thirty-month naturalistic follow-up study of early-onset dysthymic disorder: Course, diagnostic stability, and prediction of outcome. Journal of Abnormal Psychology, 107, 338–348.


Klerman, G. L., DiMascio, A., Weissman, M. M., Prusoff, B. A., & Paykel, E. S. (1974). Treatment of depression by drugs and psychotherapy. American Journal of Psychiatry, 131, 186–191.


Kovacs, M. (1992). Children’s depression inventory manual. Toronto, Canada: Multihealth Systems.


Lewinsohn, P. M., Hops, H., Roberts, R. E., & Seeley, J. R. (1993). Adolescent psychopathology: I. Prevalence and incidence of depression and other DSM-III-R disorders in high school students. Journal of Abnormal Psychology, 102, 133.


Lewinsohn, P. M., Roberts, R. E., Seeley, J. R., Rohde, P., Gotlib, I. H., & Hops, H. (1994). Adolescent psychopathology: II. Psychosocial risk factors for depression. Journal of Abnormal Psychology, 103, 302–315.


Lewinsohn, P. M., Rohde, P., & Seeley, J. R. (1998). Treatment of adolescent depression: Frequency of services and impact on functioning in young adulthood. Depression and Anxiety, 7, 47–52.


Markowitz, J. C., Weissman, M. M., & Gabbard, G. O. (2009). Applications of individual interpersonal psychotherapy to specific disorders: Efficacy and indications. In Textbook of psychotherapeutic treatments (pp. 339–364). Arlington, VA: American Psychiatric Association.


McLeod, J. D., Kessler, R. C., & Landis, K. R. (1992). Speed of recovery from major depressive episodes in a community sample of married men and women. Journal of Abnormal Psycholology, 101, 277.


Miller, I. W., Keitner, G. I., Ryan, C. E., Solomon, D. A., Cardemil, E. V., & Beevers, C. G. (2005). Treatment matching in the posthospital care of depressed patients. American Journal of Psychiatry, 162, 2131–2138.


Miller, I. W., Ryan, C. E., Keitner, G. I., Bishop, D. S., & Epstein, N. B. (2000). The McMaster approach to families: Theory, assessment, treatment and research. Journal of Family Therapy, 22, 168–189.


Moncrieff, J., & Kirsch, I. (2005). Efficacy of antidepressants in adults. BMJ, 331, 155–157.


Mufson, L., Dorta, K. P., Wickramaratne, P., Nomura, Y., Olfson, M., & Myrna, M. W. (2004). A randomized effectiveness trial of interpersonal psychotherapy for depressed adolescents. Archives of General Psychiatry, 61, 577.


Mufson, L., Moreau, D., Weissman, M. M., & Klerman, G. L. (1993). Interpersonal psychotherapy for depressed adolescents. New York, NY: Guilford.


Mufson, L., Weissman, M. M., Moreau, D., & Garfinkel, R. (1999). Efficacy of interpersonal psychotherapy for depressed adolescents. Archives of General Psychiatry, 56, 573–579.


Nolen Hoeksema, S., & Girgus, J. S. (1994). The emergence of gender differences in depression during adolescence. Psychological Bulletin, 115, 424–443.


Pampallona, S., Bollini, P., Tibaldi, G., Kupelnick, B., & Munizza, C. (2004). Combined pharmacotherapy and psychological treatment for depression: A systematic review. Archives of General Psychiatry, 61, 714–719.


Philip, S. W., Gregory, S., & Ronald, C. K. (2003). The economic burden of depression and the cost-effectiveness of treatment. International Journal of Methods in Psychiatric Research, 12, 22–33.


Prinstein, M. J., Borelli, J. L., Cheah, C. S. L., Simon, V. A., & Aikins, J. W. (2005). Adolescent girls’ interpersonal vulnerability to depressive symptoms: A longitudinal examination of reassurance-seeking and peer relationships. Journal of Abnormal Psychology, 114, 676.


Radloff, L. S. (1977). The CES-D scale: A self-report depression scale for research in the general population. Applied Psychological Measurement, 1, 385–401.


Rohde, P., Beevers, C. G., Stice, E., & O’Neil, K. (2009). Major and minor depression in female adolescents: Onset, course, symptom presentation, and demographic associations. Journal of Clinical Psychology, 65, 1339–1349.


Rosselló, J., & Bernal, G. (1999). The efficacy of cognitive-behavioral and interpersonal treatments for depression in Puerto Rican adolescents. Journal of Consulting and Clinical Psychology, 67, 734–745.


Rush, A. J., Thomas, C., & Paul-Egbert, R. (2000). The inventory of depressive symptomatology (IDS): Clinician (IDS-C) and self-report (IDS-SR) ratings of depressive symptoms. International Journal of Methods in Psychiatric Research, 9, 45–59.


Rush, A. J., Trivedi, M. H., Ibrahim, H. M., Carmody, T. J., Arnow, B., Klein, D. N.,…Markowitz, J. C. (2003). The 16-item quick inventory of depressive symptomatology (QIDS), clinician rating (QIDS-C), and self-report (QIDS-SR): A psychometric evaluation in patients with chronic major depression. Biological Psychiatry, 54, 573–583.


Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S.,…Weistaub, N. (2003). Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants. Science, 301, 805–809.


Seeley, J. R., Stice, E., & Rohde, P. (2009). Screening for depression prevention: Identifying adolescent girls at high risk for future depression. Journal of Abnormal Psychology, 118, 161–170.


Sheehan, D. V., Lecrubier, Y., Sheehan, K. H., Amorim, P., Janavs, J., Weiller, E.,…Hergueta, T. (1998). The mini-international neuropsychiatric interview (M.I.N.I): The development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. Journal of Clinical Psychiatry, 59, 22.


Sheehan, D. V., Lecrubier, Y., Sheehan, K. H., Janavs, J., Weiller, E., Keskiner, A.,…Schnika, J. (1997). The validity of the mini international neuropsychiatric interview (MINI) according to the SCID-P and its reliability. European Psychiatry, 12, 232.


Stahl, S. M., Entsuah, R., & Rudolph, R. L. (2002). Comparative efficacy between venlafaxine and SSRIs: a pooled analysis of patients with depression. Biological Psychiatry, 52, 1166–1174.


Teichman, Y., Bar-El, Z., Shor, H., & Sirota, P. (1995). A comparison of two modalities of cognitive therapy (individual and marital) in treating depression. Psychiatry: Interpersonal and Biological Processes, 58, 136–148.


Thase, M. E., Greenhouse, J. B., Frank, E., Reynolds, C. F., III, Pilkonis, P. A., Hurley, K.,…Grochocinski, V. (1997). Treatment of major depression with psychotherapy or psychotherapy-pharmacotherapy combinations. Archives of General Psychiatry, 54, 1009–1015.


Treatment for Adolescents with Depression Study Team. (2003). Treatment for adolescents with depression study (TADS): Rationale, design, and methods. Journal of the American Academy of Child and Adolescent Psychiatry, 42, 531–542.


Treatment for Adolescents with Depression Study Team. (2004). Fluoxetine, cognitive-behavioral therapy, and their combination for adolescents with depression: Treatment for adolescents with depression study (TADS) randomized controlled trial. JAMA, 292, 807–820.


Treatment for Adolescents with Depression Study Team. (2007). The treatment for adolescents with depression study (TADS): Long-term effectiveness and safety outcomes. Archives of General Psychiatry, 64, 1132–1143.


Trivedi, M. H., Rush, A. J., Wisniewski, S. R., Nierenberg, A. A., Warden, D., Ritz, L.,…Norquist, G. (2006). Evaluation of outcomes with citalopram for depression using measurement-based care in STAR∗D: Implications for clinical practice. American Journal of Psychiatry, 163, 28–40.


Weissman, M. M., Leaf, P. J., Bruce, M. L., & Florio, L. (1988). The epidemiology of dysthymia in five communities: Rates, risks, comorbidity, and treatment. American Journal of Psychiatry, 145, 815–819.


Weissman, M. M., Markowitz, J. C., & Klerman, G. L. (2000). Comprehensive guide to interpersonal psychotherapy. New York, NY: Basic Books.


Weissman, M. M., Prusoff, B. A., DiMascio, A., Neu, C., Goklaney, M., & Klerman, G. L. (1979). The efficacy of drugs and psychotherapy in the treatment of acute depressive episodes. American Journal of Psychiatry, 136, 555–558.


Wells, K. B., Burnam, M. A., Rogers, W., Hays, R., & Camp, P. (1992). The course of depression in adult outpatients: Results from the medical outcomes study. Archives of General Psychiatry, 49, 788–794.


Wilfley, D. E., MacKenzie, R. K., Welch, R. R., Ayres, V. E., & Weissman, M. M. (2000). Interpersonal psychotherapy for groups. New York, NY: Basic Books.


Stay updated, free articles. Join our Telegram channel

Aug 10, 2016 | Posted by in PSYCHOLOGY | Comments Off on Introduction: Evidence-Based Practice for Major Depressive Disorder

Full access? Get Clinical Tree

Get Clinical Tree app for offline access