d-Cycloserine as an Augmentation Strategy With Cognitive-Behavioral Therapy for Social Anxiety Disorder

Participants were recruited between September 2007 and June 2011 through referrals to the three study sites (Boston University [BU], Massachusetts General Hospital [MGH], and Southern Methodist University [SMU]), from other area clinical facilities and programs, and through advertisements. Participants had to be at least 18 years of age; have a current DSM-IV diagnosis of generalized social anxiety disorder that the patient designated as the most important source of current distress or interference; have a score ≥60 on the Liebowitz Social Anxiety Scale (29); have no clinically significant abnormalities based on physical examination, ECG, and laboratory findings; and be willing and able to comply with the requirements of the study protocol. Exclusion criteria included a lifetime history of bipolar disorder, schizophrenia, psychosis, delusional disorders, or OCD; an eating disorder in the past 6 months; organic brain syndrome, mental retardation, or other cognitive dysfunction that could interfere with the capacity to engage in therapy; a history of substance abuse or dependence (other than nicotine or caffeine) in the past 6 months or otherwise unable to commit to refraining from alcohol use during the treatment period of the study; PTSD within the past 6 months (entry of patients with other mood or anxiety disorders was permitted if the social anxiety disorder was judged to be the predominant disorder, in order to increase accrual of a clinically relevant sample); significant suicidal ideation as suggested by a score ≥3 on item 10 of the Montgomery-Åsberg Depression Rating Scale (30) (or presence of suicidal behaviors within the past 6 months; concurrent psychotropic medication (e.g., antidepressants, anxiolytics, beta-blockers) for at least 2 weeks prior to entering the study; significant personality dysfunction likely to interfere with study participation; serious medical illness or instability for which hospitalization may be likely during the following year; any history of seizures; pregnant or lactating women and women of childbearing potential who are not using medically accepted forms of contraception; any concurrent psychotherapy initiated within 3 months of baseline or ongoing psychotherapy of any duration directed specifically toward treatment of social anxiety disorder (prohibited psychotherapy included CBT or psychodynamic therapy focusing on exploring specific, dynamic causes of the phobic symptomatology and providing management skills; general supportive therapy initiated more than 3 months before baseline was acceptable); prior nonresponse to adequately delivered exposure (as defined by the patient’s report of receiving specific and regular exposure assignments as part of a previous treatment); a history of head trauma causing loss of consciousness, seizure, or ongoing cognitive impairment; current treatment with isoniazid; and inability to understand study procedures and participate in the informed consent process.

Study participants underwent a two-step screening evaluation, consisting of an initial telephone screen and then a psychiatric assessment, medical history, and physical examination. (A CONSORT diagram of participant flow is available in the data supplement that accompanies the online edition of this article). Patients in the d-cycloserine-augmented CBT group did not differ from the placebo-augmented CBT group in mean age (34.6 years and 30.5 years, respectively). Table 1 summarizes other demographic information for patients who were assigned to a treatment group. The two treatment groups did not differ in any of the demographic data at baseline, except that there were more males in the d-cycloserine group than in the placebo group (64% and 49%, respectively; two-tailed Fisher’s exact test, p=0.045).

Eligible participants were enrolled in a 12-session CBT protocol across three study sites (BU, MGH, and SMU), all using identical study protocols. One of the sites (MGH) is well known for conducting pharmacological studies, whereas the SMU and BU sites specialize in providing psychological interventions. At session 3, patients were randomly assigned to receive oral administration of either 50 mg of d-cycloserine (N=87) or pill placebo (N=82) 1 hour prior to the start of sessions 3–7. Assignment to treatment condition was determined by a computer-generated allocation schedule with stratification by baseline severity of social anxiety disorder (i.e., Liebowitz Social Anxiety Scale score <70 or ≥70) (29). Assessments of primary outcome variables were conducted at baseline, at sessions 2 through 8, at sessions 10 and 12, after treatment (week 13), and at 1-month, 3-month, and 6-month follow-ups (weeks 17, 25, and 37, respectively). The trial was sufficiently powered to detect a medium-sized effect (d=0.5) at 85% power and a significance threshold of 0.05 at the posttreatment (week 13) assessment. It was also sufficiently powered to detect a medium-sized group difference (d=0.5) at 80% power and a significance threshold of 0.05 at the 6-month follow-up, which was the assessment with the smallest number of participants available for the analyses. The protocol was approved by the institutional review boards of the three participating sites. Participants provided written informed consent after receiving a complete description of the study.

Initial diagnoses were performed by trained study therapists using the Structured Clinical Interview for DSM-IV (31) at the MGH and SMU sites and the Anxiety Disorders Interview Schedule for DSM-IV (32) at the BU site. In addition, the Liebowitz Social Anxiety Scale was administered to assess for the generalized social anxiety disorder diagnostic subtype specifier. The blinded assessments were conducted by a master’s- or doctoral-level clinician trained in these assessments. The integrity and reliability of the diagnostic and efficacy evaluations was established through training by the MGH site and maintained by providing the clinicians with weekly supervision and feedback based on approximately 20% of the audiorecorded assessment interviews.

The primary outcome measures were Clinical Global Impression ratings tailored to social anxiety as assessed by the Liebowitz Social Anxiety Scale rating scale (29) and the Social Phobic Disorders Severity and Change Form (33), which yielded two continuous measures, a Social Phobic Disorders Severity score and a Social Phobic Disorders Change score. These scores are the Clinical Global Impression scores (severity and improvement, respectively) with the wording modified specifically to measure symptoms of social anxiety disorder (33). These clinical interviews were conducted by an interviewer blind to treatment assignment.

Response was defined as an improvement score of 1 (“very much improved”) or 2 (“much improved”) on the Social Phobic Disorders Change scale; remission was defined as an improvement score of 1 or 2 on the Social Phobic Disorders Change scale and a score <30 on the Liebowitz Social Anxiety Scale.

The primary analyses were conducted using mixed-effects regression models for continuous outcome variables (Social Phobic Disorders Severity and Liebowitz Social Anxiety Scale scores), and generalized linear mixed models (mixed-effects regression models using a logistic linking function) for dichotomous outcomes (remission and response). These analytical approaches allow the inclusion of all subjects, regardless of missing data, thereby improving statistical power and the generalizability of the results, and they are the recommended approaches to analyzing longitudinal psychiatric data (37). Because the growth curve of the outcome measures changed markedly from treatment through follow-up, the curve was modeled as “discontinuous” (38), allowing all growth curve parameters to change from the treatment phase to the follow-up phase. The predictors in the models were time (t), t², treatment condition (T), T×t and T×t². In addition, because of the disproportionally higher rate of males in the d-cycloserine-augmented CBT condition, sex along with the interaction of sex and time were added as additional covariates in the model. Because initial severity is likely to be related to rate of improvement in outcomes, we also included initial severity and the interaction of initial severity with time as additional predictors of outcome to reduce variance in outcome. The growth curves during the treatment phase and the follow-up periods were linear for both of the continuous outcome measures (Social Phobic Disorders Severity and Liebowitz Social Anxiety Scale scores) but were curvilinear for the treatment phase in the analysis of the dichotomous outcomes (remission and response). Thus, the quadratic terms for the growth curve were omitted from the mixed-effects regression model analyses of Social Phobic Disorders Severity and Liebowitz Social Anxiety Scale scores and retained in the generalized linear mixed-model analyses for the treatment phase of the analysis of response and remission. Neither sex nor the interaction of sex and time were significant predictors of any of the outcomes.

Attrition rates during the 12-week treatment phase were low and did not differ significantly between groups (10.3% for the d-cycloserine-augmented CBT group and 15.9% for the placebo-augmented CBT group). (The reasons for attrition are listed in the flow diagram in the online data supplement.) Similarly, attrition was low during the follow-up phase (11.5% and 11.0% for the d-cycloserine and placebo groups, respectively). The mean number of CBT sessions attended was 10.8 (SD=2.19) in the d-cycloserine-augmented condition and 10.6 (SD=2.14) in the placebo-augmented condition. Similarly, compliance with pill administration was high, with 78.1% of patients receiving all pill administrations (d-cycloserine group, 75.9%; placebo group, 80.5%).

At the beginning of sessions 3–7 when the study pills were administered, patients were asked to indicate whether they believed the pill contained d-cycloserine or placebo or whether they were unable to guess. Approximately one-third to one-half of all patients (30.9%–46.2%, depending on group and session) in both conditions reported that they were unable to guess their treatment condition (all chi-square tests, n.s.). Among patients who guessed either of the two drug conditions, those who received d-cycloserine did not differ significantly from those who received placebo in their guess that they received d-cycloserine, in any of the sessions.

There were no differences between groups at baseline on Liebowitz Social Anxiety Scale score (mean=81.34 [SD=15.06] compared with mean=81.98 [SD=17.15]), Social Phobic Disorders Severity score (mean=5.33 [SD=0.83] compared with mean=5.26 [SD=0.86]) or depressive symptom severity. The median number of comorbid diagnoses in both groups was 1.

An intent-to-treat analysis using the last-observation-carried-forward approach revealed response rates of 79.3% in the d-cycloserine-augmented group and 73.2% in the placebo-augmented group (Table 2). The remission rates of these intent-to-treat analyses were 34.5% and 24.4% for the d-cycloserine and placebo groups, respectively. The difference between groups was not statistically significant for either response or remission rate.

The follow-up analyses using traditional intent-to-treat analyses also revealed no significant differences between the d-cycloserine-augmented and placebo-augmented groups in response rates at the 1-month follow-up (74.7% and 75.6%, respectively), the 3-month follow-up (73.6% and 70.7%, respectively), or the 6-month follow-up (70.1% and 74.4%, respectively). Similarly, these analyses revealed no between-group differences for remission rates at the 1-month follow-up (33.3% and 28.0%, respectively), the 3-month follow-up (29.9% and 28.0% respectively), or the 6-month follow-up (29.9% and 28.0%, respectively).

The mixed-effects regression models revealed that at the posttreatment assessment, the d-cycloserine-augmented group had lower mean global illness severity scores, as measured with the Social Phobic Disorders Severity score, than the placebo-augmented group (estimated parameter for treatment effect: 0.43; t=2.05, df=149, p=0.04). We also observed a statistical trend toward lower scores in the Liebowitz Social Anxiety Scale at the posttreatment assessment with d-cycloserine compared with placebo (estimated parameter for treatment effect: 5.22; t=1.75, df=146, p=0.08). Unadjusted means and 95% confidence intervals are presented in Table 2.

During the treatment phase, patients who received d-cycloserine-augmented CBT exhibited a faster slope of improvement on global illness severity (Social Phobic Disorders Severity scores; estimated parameter for treatment effect: 0.06; t=2.76, df=129, p=0.006) (Figure 1), on social anxiety symptom severity scores (Liebowitz Social Anxiety Scale; estimated parameter for treatment effect: 0.65; t=2.18, df=147, p=0.03), and on remission rates (estimated parameter for treatment effect: –0.10; t=2.59, df=1661, p=0.01) as compared with those who received placebo-augmented CBT. Compared with patients in the placebo group, those in the d-cycloserine group showed a 33% faster rate of improvement in Social Phobic Disorders Severity scores, a 24% faster reduction in Liebowitz Social Anxiety Scale scores, and a 30% faster increase in remission rates during treatment. There was no between-group difference on slopes of change in response rates.

During the follow-up period, the mixed-effects regression model and generalized linear mixed-model analyses showed that none of the slopes of change for any of the outcome measures (Social Phobic Disorders Change scores, Liebowitz Social Anxiety Scale, response, and remission) varied as a function of condition. Patients receiving d-cycloserine did not evidence significantly better outcomes on any of the measures at the posttreatment or follow-up assessments. Unadjusted means and 95% confidence intervals are presented in Table 2.