- Anxiety sensitivity, experiential avoidance and emotion regulation difficulties moderated outcomes; higher scores showed greater benefit from group CBT/ERP than ACT.
- Findings contradicted hypotheses and highlight the need to investigate the active mechanisms of ACT.
- Group therapeutic alliance predicted and moderated treatment outcomes across both group CBT/ERP and ACT.
Psychother Res. 2026 May 15:1-13. doi: 10.1080/10503307.2026.2671186. Online ahead of print.
ABSTRACT
AIM: This study examined theory-driven predictors and moderators of treatment outcomes in group-based cognitive behavioral therapy with exposure and response prevention (CBT/ERP) and acceptance and commitment therapy (ACT) for obsessive-compulsive disorder (OCD).
METHOD: A total of 176 adults diagnosed with OCD according to DSM-5 criteria were randomized to either group-based CBT/ERP or ACT. Participants received 14 weekly sessions and were assessed using clinical interviews at baseline, post-treatment, and 6- and 12-month follow-ups.
RESULTS: Anxiety sensitivity, experiential avoidance, and emotion regulation difficulties significantly moderated treatment response, with individuals high on these dimensions benefiting more from CBT/ERP than ACT.
CONCLUSION: These findings were contrary to our hypotheses and underline the importance of investigating the active mechanisms of ACT. Additionally, group therapeutic alliance predicted and moderated treatment outcomes across both interventions.
CLINICAL OR METHODOLOGICAL SIGNIFICANCE OF THIS ARTICLE: This study provides preliminary evidence that anxiety sensitivity, experiential avoidance, and emotion regulation difficulties significantly moderated treatment response, with individuals scoring higher on these dimensions deriving greater benefit from CBT/ERP compared with ACT. These findings were contrary to our hypotheses and underscore the need for further investigation into the mechanisms of action underlying ACT. In addition, group therapeutic alliance moderated outcomes across both interventions.
PMID:42138010 | DOI:10.1080/10503307.2026.2671186
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