In an experimental design using convenience sampling, adults with OCD were recruited from outpatients of clinics in Tehran, Iran, from February 2012 to March 2013. The study was approved by the Ethics Committee of Tehran University of Medical Sciences. A written informed consent was obtained from patients and received complete descriptions regarding the study procedures. Inclusion criteria for the sample were: a) a primary diagnosis of OCD according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) (
19); b) age between 18 and 50 years; and c) OC symptoms duration of at least one year. Patients were excluded from the study if they: a) had a current or past psychotic disorder; b) had suicidal tendencies; c) had a medical illness; d) had a substance abuse disorder; e) had a personality disorder and f) had been treated with either pharmacotherapy or psychotherapy in the last one month. Forty-four patients were referred for treatment, of which 40 met the DSM-IV-TR criteria for OCD. They were interviewed by a structured clinical interview for DSM-IV axis I disorders, patient edition (SCID-I/P version 2) (
20) and a structured clinical interview for DSM-IV axis II disorders (SCID-II) (
21) to verify the diagnosis by an independent evaluator (PhD level clinical psychologist). Two patients with bipolar disorder, two patients with psychotic disorder, one patient with avoidant personality disorder, two patients with OC personality disorder and one patient with borderline personality disorder were excluded from the study. In all, 32 patients fitted the inclusion/exclusion criteria and were randomly assigned to receive ACT (n = 10), SSRIs (n = 11) or combination of ACT and SSRIs (n = 11). Five patients did not complete the study. Three patients dropped out the drug group; one because of not tolerating adverse effects of sertraline and two for irregular use of fluoxetine. One patient abandoned the ACT group for needing SSRI during the treatment phase. One patient dropped out of the combination group for unknown reasons.
The mean age of the final sample (n = 27) was 26.96 ± 6.83 years; 55.6% (n = 15) of the patients were men and 44.4% (n = 12) women. Duration of OC symptoms ranged between 1 and 16 years. The Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) total and Acceptance and Action Questionnaire (AAQ) scores (mean ± standard deviation) for the sample were 24.40 ± 3.07 and 36.20 ± 6.08, respectively. All patients met the criteria for OCD as their primary diagnosis with 33.3% receiving one additional diagnosis. The frequency of comorbidities in each treatment condition was as follows; major depressive disorder and dysthymia, two ACT, two SSRIs, two ACT plus SSRIs; anxiety disorders, one ACT, one SSRI, one ACT plus SSRIs. OCD subtypes for the sample were washing, checking, ordering, religious/sexual/aggressive thoughts and hoarding.
ACT was based on an ACT manual for OCD developed by Twohig (
14). A PhD clinical psychologist (the first author) provided ACT under the supervision of an experienced clinical psychologist in treating OCD. The ACT program included evaluating patientās obsessions and compulsions (session 1); The āMan in the holeā metaphor was used to illustrate how patientās efforts to regulate obsessions are ineffective (session 2); The āTow scalesā metaphor was used to illustrate possible benefits of acceptance of obsessions and anxiety rather than attempting to control or reduce them (sessions 3 and 4); using defusion, contact with present or mindfulness, and self as context exercises (sessions 5 and 6); recognize his values; and preventing relapse (sessions 7 and 8). Patients in drug group received a different SSRI (sertraline = 50 - 200 mg/d; fluoxetine = 20 - 80 mg/d) for 10 weeks, which was monitored by two psychiatrists. The combination group received both ACT and a different SSRI (sertraline = 50 - 200 mg/d; fluoxetine = 20 - 80 mg/d) for 10 weeks. Studies showed equivalent efficacy for different SSRIs in OCD (
2). In this study, we did not compare the efficacy of sertraline with fluoxetine on each outcome measure at the end of treatment.
SCID-I/P and SCID-II are widely used as gold standard instruments for diagnosing axis I and axis II disorders (
22). All participants were initially assessed using the SCID-I/P and SCID-II. Clinical symptoms were assessed using the Y-BOCS (
23,
24), AAQ (
25) at the beginning and end of treatment.
Y-BOCS is a 10-item clinician administered scale used for the assessment of severity of OC symptoms. It has good psychometric properties and has shown excellent treatment sensitivity (
23,
24,
26,
27). AAQ is a 9-item self-report scale, which assesses EA. Each item is rated on a 7-point scale with higher scores indicating greater EA (range: 7 - 63). It has demonstrated good internal consistency (α = 0.70) and test-retest reliability over a 4-month interval (rs = 0.64) (
24). The reliability and validity of the Iranian version of the Y-BOCS (
28), AAQ (
29), SCID-I/P and SCID-II (
30) have been evaluated and shown to be as good as their original versions.
The criteria for clinically significant change (CSC) considered a Y-BOCS total score reduction of eight scores or more from pre-treatment to post-treatment and a final Y-BOCS total score ⤠14. Patients who achieved CSC were defined as recovered. Patients were classified as improved if they achieved reliable change that is eight score or more, but scoring above 14 on Y-BOCS total. Patients who did not achieve reliable change on the Y-BOCS were defined as unchanged (
6). Full remission was defined as post-treatment Y-BOCS total score ⤠8 (
31).
Group differences were evaluated using chi-square, one-way analysis of variance (ANOVA) and one-way analysis of covariance (ANCOVA) statistical procedures on each of the outcome measures using SPSS for Windows (version 16.0, SPSS Inc., Chicago, IL, USA) statistical package.