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Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan

Primary Purpose

Bipolar Disorder

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Psycho education
Sponsored by
Pakistan Institute of Living and Learning
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring Psycho-education, Bipolar , cultural adaptation, Pakistan

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Dow University of Health Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

Psycho-education Sessions will be offered weekly basis

Patients who will be randomized to the "treatment as usual" arm will receive routine care

Outcomes

Primary Outcome Measures

Young Mania Rating Scale(YMRS)
The Young Mania Rating Scale (YMRS) is one of the most frequently utilized rating scales to assess manic symptoms
Knowledge and attitudes
Knowledge and attitudes towards bipolar disorder measured by using a standard questionnaire
Beck's Depression Inventory Scale (BDI)
The 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 Outcome Measures

Medication adherence
Self-reported Measure of Medication adherence
Visual Analogue Scale
Patient satisfaction with overall care
Short Explanatory Model Interview
used to elicit beliefs of mental illness

Full Information

First Posted
August 5, 2014
Last Updated
December 21, 2016
Sponsor
Pakistan Institute of Living and Learning
Collaborators
University of Manchester, Dow University of Health Sciences, Abbasi Shaheed Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02210390
Brief Title
Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan
Official Title
Feasibility RCT of the Efficacy of a Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
June 2012 (undefined)
Primary Completion Date
May 2015 (Actual)
Study Completion Date
May 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pakistan Institute of Living and Learning
Collaborators
University of Manchester, Dow University of Health Sciences, Abbasi Shaheed Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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 : To determine effectiveness of educational intervention in terms of patient Satisfaction with overall care, knowledge and attitudes to bipolar disorder and medication adherence. 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 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
Keywords
Psycho-education, Bipolar , cultural adaptation, Pakistan

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Psycho-education Sessions will be offered weekly basis
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients who will be randomized to the "treatment as usual" arm will receive routine care
Intervention Type
Behavioral
Intervention Name(s)
Psycho education
Intervention Description
Psycho-education Sessions will be offered weekly basis
Primary Outcome Measure Information:
Title
Young Mania Rating Scale(YMRS)
Description
The Young Mania Rating Scale (YMRS) is one of the most frequently utilized rating scales to assess manic symptoms
Time Frame
three months
Title
Knowledge and attitudes
Description
Knowledge and attitudes towards bipolar disorder measured by using a standard questionnaire
Time Frame
three months
Title
Beck's Depression Inventory Scale (BDI)
Description
The BDI is a measure of depression severity and has been used in several previous studies in Pakistan and is validated for use in Urdu.
Time Frame
three months
Secondary Outcome Measure Information:
Title
Medication adherence
Description
Self-reported Measure of Medication adherence
Time Frame
three months
Title
Visual Analogue Scale
Description
Patient satisfaction with overall care
Time Frame
three months
Title
Short Explanatory Model Interview
Description
used to elicit beliefs of mental illness
Time Frame
three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nusrat Husain, MD
Organizational Affiliation
Pakistan Institute of Learning and Living, University of Manchester
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Imran Chaudhry, MD
Organizational Affiliation
University of Manchester
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Farooq Naeem, MRCPsych
Organizational Affiliation
Pakistan Institute of Learning and Living, University of Southampton
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Raza Ur Rehman, FCPS
Organizational Affiliation
Dow University of Health Sciences
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ajmal kazm
Organizational Affiliation
Pakistan Institute of Living and Learning
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Munir Hamirani, FCPS
Organizational Affiliation
Abbasi Shaheed Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Muhammad I Husain, MRCPsych
Organizational Affiliation
Camden and Islington NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dow University of Health Sciences
City
Karachi
State/Province
Sindh
Country
Pakistan

12. IPD Sharing Statement

Citations:
PubMed Identifier
28155203
Citation
Husain MI, Chaudhry IB, Rahman RR, Hamirani MM, Mehmood N, Haddad PM, Hodsoll J, Young AH, Naeem F, Husain N. Pilot study of a culturally adapted psychoeducation (CaPE) intervention for bipolar disorder in Pakistan. Int J Bipolar Disord. 2017 Dec;5(1):3. doi: 10.1186/s40345-017-0074-8. Epub 2017 Feb 11.
Results Reference
derived

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Culturally Adapted Psychological Intervention for Bipolar Disorder in Pakistan

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