Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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29 August 2016 |
Main ID: |
NCT02797691 |
Date of registration:
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26/05/2016 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Developing and Testing of Culturally Adapted Cognitive Behavior Therapy (CaCBT) for Pashto Speaking Pakistanis and Afghans
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Scientific title:
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Developing and Testing of Culturally Adapted Cognitive Behavior Therapy (CaCBT) for Pashto Speaking Pakistanis and Afghans |
Date of first enrolment:
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January 2016 |
Target sample size:
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40 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT02797691 |
Study type:
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Interventional |
Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Pakistan
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Contacts
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Name:
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Muhammad Irfan, MCPS FCPS MS |
Address:
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Telephone:
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Email:
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Affiliation:
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Peshawar Medical College |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- All those who fulfill the diagnostic criteria of Depressive episode (F32) or
Recurrent depressive disorder (F33 except 33.4) or Anxiety disorder using ICD10 RDC
and who live within travelling distance of the psychiatry department in Peshawar will
be approached. Those patients, who have agreed to enter the study, will be assessed 2
weeks later, to fill in the baseline measures when they attend their first
appointment. Patients will be asked to attend a further appointment at the end of
study period and will be assessed again.
Exclusion Criteria:
- Excessive use of alcohol or drugs (using ICD 10 RDC for alcohol or drug abuse or
dependence) significant cognitive impairment (for example learning disability or
dementia) and active psychosis.
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Depression, Anxiety
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Intervention(s)
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Other: CaCBT
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Other: Medication/ Psychotherapy
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Primary Outcome(s)
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Change in score of Hospital Anxiety and Depression Scale (HADS) from baseline to end of therapy
[Time Frame: 2 Months]
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Secondary Outcome(s)
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Change in score of Bradford Somatic Inventory (BSI) from baseline to end of therapy
[Time Frame: 2 Months]
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Change in score of Brief Disability Questionnaire/ WHO DAS from baseline to end of therapy
[Time Frame: 2 Months]
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Secondary ID(s)
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CBT Pashtu 1
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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