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Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan

Feasibility RCT of the Efficacy of a Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02210390
Enrollment
36
Registered
2014-08-06
Start date
2012-06-30
Completion date
2015-05-31
Last updated
2016-12-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder

Keywords

Psycho-education, Bipolar , cultural adaptation, Pakistan

Brief summary

Aim: To assess the Feasibility RCT of the efficacy of a culturally adapted psychological intervention for Bipolar disorder in Pakistan Design: Randomized Control Trial Setting: Psychiatric Departments of different Hospitals in Karachi. Participants: A total of 36 Bipolar disorder patients will be randomized to psychological Intervention and treatment as usual arm. Intervention: Culturally Adapted psychological intervention for bipolar disorder Outcome measure: * Acceptance of intervention in terms of attending session and dropouts * Knowledge and attitudes towards bipolar disorder

Detailed description

The purpose of the study is to test Feasibility RCT of the efficacy of a culturally adapted psychological intervention for Bipolar disorder in Pakistan Primary Objectives : 1. To determine effectiveness of educational intervention in terms of patient Satisfaction with overall care, knowledge and attitudes to bipolar disorder and medication adherence. 2. To assess feasibility in terms of * Recruitment * Using instruments that will be used to assess recurrence rate in the main study (BDI, YMRS and obtaining prospective hospitalisation and medication data) * acceptability of a culturally adapted bipolar group education package 3. To allow 'fine tuning' of culturally adapted bipolar group education package (this will partly be achieved by using the SEMI at study entry) The Participants will be recruited from psychiatric department of different hospitals. They will be randomly divided into two groups; intervention group and treatment-as-usual group. A total of thirty six participants will be recruited in the pilot study and divided equally into two arms. This will ensure that, even after loss to follow-up, we will have at least 12 subjects per group for analysis (FDA guidance http://www.fda.gov/cder/guidance/5356fnl.pdf) .Randomization will be carried out by the on offsite statistician. This will provide a reliable geographically remote service. For intervention group twelve sessions of psychoeducation will be provided by trained research clinician during the period of three months. Patients in the treatment as usual (TAU) group will be given details of intervention at the end of the study and interested patients will be offered psychoeducation.

Interventions

BEHAVIORALPsycho education

Psycho-education Sessions will be offered weekly basis

Sponsors

University of Manchester
CollaboratorOTHER
Dow University of Health Sciences
CollaboratorOTHER
Abbasi Shaheed Hospital
CollaboratorOTHER
Pakistan Institute of Living and Learning
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of DSM IV Bipolar disorder * Currently stable (YMRS \<8, BDI\<12) * Age 18 to 65 years. * Participants engaged with the mental health services since last 6 months. * Able to give written informed consent. * Resident of trial catchments area * Ability to speak Urdu /Punjabi

Exclusion criteria

* Substance or alcohol dependent (i.e., those who fulfill the criteria for dependence according to DSM IV criteria) * Inability to engage fully in the psychotherapy (due to cognitive impairment) * Actively suicidal * Any major psychiatric illness other than bipolar disorder

Design outcomes

Primary

MeasureTime frameDescription
Young Mania Rating Scale(YMRS)three monthsThe Young Mania Rating Scale (YMRS) is one of the most frequently utilized rating scales to assess manic symptoms
Knowledge and attitudesthree monthsKnowledge and attitudes towards bipolar disorder measured by using a standard questionnaire
Beck's Depression Inventory Scale (BDI)three monthsThe BDI is a measure of depression severity and has been used in several previous studies in Pakistan and is validated for use in Urdu.

Secondary

MeasureTime frameDescription
Medication adherencethree monthsSelf-reported Measure of Medication adherence
Visual Analogue Scalethree monthsPatient satisfaction with overall care
Short Explanatory Model Interviewthree monthsused to elicit beliefs of mental illness

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026