Brief Culturally Adapted CBT for OCD
Brief Culturally Adapted Cognitive Behaviour Therapy (CaCBT) for Obsessive-Compulsive Disorder: A Randomised Controlled Trial From Pakistan
1 other identifier
interventional
166
1 country
1
Brief Summary
The purpose aims to assess the efficacy of Brief Culturally Adapted Cognitive Behaviour Therapy (Ca-CBT) for the treatment of Obsessive Compulsive Disorder (OCD).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 16, 2024
CompletedStudy Start
First participant enrolled
October 20, 2024
CompletedFirst Posted
Study publicly available on registry
November 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 10, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedNovember 18, 2025
November 1, 2025
1.1 years
October 16, 2024
November 15, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Efficacy of brief culturally adapted cognitive behaviour therapy (CaCBT) for OCD
By comparing pre- and post-treatment OCD scores measured through the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS).
6 weeks
Acceptability of the brief culturally adapted cognitive behaviour therapy (CaCBT) for OCD
Feedback will be taken from both patients and their family members, who will be trained as co-therapists, to evaluate their satisfaction with the therapy.
6 weeks
Secondary Outcomes (2)
Reduction in depression and anxiety associated with OCD
6 weeks
Reduction in functioning decline associated with OCD
6 weeks
Study Arms (2)
Brief culturally adapted CBT (CaCBT) group
EXPERIMENTALParticipants in this group will receive the Culturally Adapted CBT (CaCBT) manual along with treatment as usual (which typically involves medication prescriptions and regular hospital visits). The manual will focus on psychoeducation, symptom management, Exposure and Response prevention (ERP), thought distraction techniques, relaxation exercises, detection of mood and thoughts, cognitive errors, changing negative thinking, behavioural activation, problem solving, improving relationships and communication skills, Thought diaries and progress diary.
Treatment as usual group
NO INTERVENTIONParticipants in this group will receive only treatment as usual (TAU), which typically involves medication prescriptions and regular hospital visits. Research psychologists delivering the intervention will not be involved with participants allocated to TAU.
Interventions
The intervention will focus on psychoeducation, symptom management, Exposure and Response prevention (ERP), thought distraction techniques, relaxation exercises, detection of mood and thoughts, cognitive errors, changing negative thinking, behavioural activation, problem solving, improving relationships and communication skills, Thought diaries and progress diary.
Eligibility Criteria
You may qualify if:
- Participants aged 18 years or above
- Participants with at least an elementary level of reading and writing
- Clinical diagnosis of Obsessive Compulsive Disorder, either alone or comorbid with depression or anxiety
You may not qualify if:
- Participants with excessive use of alcohol or drugs (using ICD-10 RDC for alcohol or drug abuse or dependence)
- Those with significant cognitive impairment (for example, intellectual disability or dementia)
- Or those with OCD comorbid active psychosis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Professional Association of Cognitive Therapy
Lahore, Punjab Province, 54000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Farooq Naeem
Professional Association of Cognitive Therapy
- PRINCIPAL INVESTIGATOR
Muhammad Aslam
Professional Association of Cognitive Therapy
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 16, 2024
First Posted
November 18, 2025
Study Start
October 20, 2024
Primary Completion
December 10, 2025
Study Completion
December 31, 2025
Last Updated
November 18, 2025
Record last verified: 2025-11