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Culturally Adapted Motivational Interviewing With CBT and Mindfulness Based Relapse Prevention for Substance Use Disorder in Pakistan (CAMIAB)

Primary Purpose

Substance Use Disorder (SUD)

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Motivational interviewing with CBT (MICBT)
Mindfulness based Relapse Prevention (MBRP)
CAMIAB
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 Substance Use Disorder (SUD)

Eligibility Criteria

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

Inclusion Criteria

  • Participants with substance use disorder
  • Meeting DSM-V criteria for substance use disorder
  • Age 18 years and above
  • Being able to understand spoken or written Urdu
  • Have undergone through the process of detoxification before study intervention

Exclusion Criteria

• Any evidence of organic brain disease, clinically significant cooccurring medical illness or mental illness to the extent that can impede their ability to provide informed consent or engagement in the intervention.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    Experimental

    No Intervention

    Arm Label

    Motivational Interviewing with CBT (MICBT)

    Mindfulness based Relapse Prevention Group (MBRP)

    Integrated MICBT and MBRP Group (CAMIAB)

    Treatment as usual (TAU)

    Arm Description

    Participants in this arm will receive a total of 12 weekly sessions of CBT based Motivational Interviewing over a period of 12 weeks.

    Participants in this arm will receive a total of 12 weekly sessions of mindfulness intervention over a period of 12 weeks.

    This will be integrated MICBT plus MBRP intervention. Participants will receive a total of 12 weekly sessions of this integrated CAMIAB intervention.

    This will be routine care psychological treatment that they will be receiving.

    Outcomes

    Primary Outcome Measures

    Feasibility measures
    Feasibility will be determined by recruitment rates, adherence rate and retention rates. The criterion for success of feasibility is to recruit >50% of eligible participants, adherence rate (number of home assignments completed; > 50%) and retention rate of 70%.
    Acceptability measure
    Acceptability will be determined based on the number of sessions attended by participants and success criterion for intervention acceptability is mean attendance rate of at least 8 sessions.

    Secondary Outcome Measures

    The Maudsley Addiction Profile
    The Maudsley Addiction Profile is a brief, questionnaire that measures problems in four domains: substance use, health risk behaviour, physical and psychological health, and personal/social functions.
    The Short Warwick-Edinburgh Mental Well-being Scale
    The Short Warwick-Edinburgh Mental Well-being Scale is a 7 items measure that will be used to measure mental wellbeing. It consists of 7 statements on a 5 point Likert scale. The minimum scale score is 7 and the maximum is 35. The high score indicates high mental wellbeing.
    EuroQol-5
    Quality of life will be measured using EuroQoL (EQ-5D) scale. This is a standardized instrument to measure health status and associated population utility weights. It measures five dimensions of health (mobility, self-care, usual activities, pain/ discomfort and anxiety/ depression) at different levels that include "no problems, slight problems, moderate problems, severe problems, and unable to do/extreme".
    Client service receipt inventory
    CSRI will be used to estimate the health and social services received.

    Full Information

    First Posted
    April 25, 2021
    Last Updated
    August 25, 2023
    Sponsor
    Pakistan Institute of Living and Learning
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04885569
    Brief Title
    Culturally Adapted Motivational Interviewing With CBT and Mindfulness Based Relapse Prevention for Substance Use Disorder in Pakistan (CAMIAB)
    Official Title
    Feasibility Study of Culturally Adapted Cognitive Behavioral Therapy Based Integrated Motivational Interviewing and Mindfulness Intervention for Substance Use Disorder in Pakistan (CAMIAB)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 1, 2023 (Anticipated)
    Primary Completion Date
    December 2024 (Anticipated)
    Study Completion Date
    June 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Pakistan Institute of Living and Learning

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The study has both quantitative and qualitative components. The aim of study is to: Culturally adapt and integrate the existing Motivational Interviewing with Cognitive Behavioral Therapy(MICBT) and Mindfulness based Relapse Prevention (MBRP) for people with Substance Use Disorder (SUD) in Pakistan Test the feasibility and acceptability of the integrated intervention called CAMIAB ('CAMIAB' means success in Urdu) in a randomized control trial (RCT).
    Detailed Description
    This study aims to culturally adapt the existing Motivational Interviewing with CBT (MICBT) and integrate this with Mindfulness-Based Relapse Prevention (MBRP) intervention for people with SUD and to test the feasibility, and acceptability of the intervention in a randomized control trial (RCT). First phase will be cultural adaptation of intervention through focus groups and individual interviews with key stakeholders . Phase two will be to test integrated MICBT and MBRP on a small group of participants N=12. Third phase will be a feasibility factorial randomized control trial with 260 participants with SUD (n=65). Participants will be recruited from primary care hospitals and drug rehabilitation centers in Karachi, Lahore, Rawalpindi, Hyderabad, and Peshawar Pakistan. Intervention will take place weekly over a period of 12 weeks. The intervention will consist of individual as well as group sessions. Assessments will be completed at baseline, after completion of intervention (12th week) and 24th week post randomization. All assessments will be administered by masked research assistants (RAs), not involved in delivering intervention sessions. The therapists delivering the intervention will be trained and will be provided ongoing supervisions by a senior therapist.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Substance Use Disorder (SUD)

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Motivational Interviewing with CBT (MICBT)
    Arm Type
    Experimental
    Arm Description
    Participants in this arm will receive a total of 12 weekly sessions of CBT based Motivational Interviewing over a period of 12 weeks.
    Arm Title
    Mindfulness based Relapse Prevention Group (MBRP)
    Arm Type
    Experimental
    Arm Description
    Participants in this arm will receive a total of 12 weekly sessions of mindfulness intervention over a period of 12 weeks.
    Arm Title
    Integrated MICBT and MBRP Group (CAMIAB)
    Arm Type
    Experimental
    Arm Description
    This will be integrated MICBT plus MBRP intervention. Participants will receive a total of 12 weekly sessions of this integrated CAMIAB intervention.
    Arm Title
    Treatment as usual (TAU)
    Arm Type
    No Intervention
    Arm Description
    This will be routine care psychological treatment that they will be receiving.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Motivational interviewing with CBT (MICBT)
    Intervention Description
    The culturally adapted MICBT will include approaches of motivational interviewing and offer ways of managing difficulties from a cognitive behavioural formulation.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Mindfulness based Relapse Prevention (MBRP)
    Intervention Description
    MBRP will incorporate cognitive-behavioural skills (i.e., effective coping skills, self-efficacy, and recognizing common antecedents of relapse) with mindfulness-based practices to decrease the probability of relapse by increasing awareness and flexible responding in the presence of substance use triggers.
    Intervention Type
    Behavioral
    Intervention Name(s)
    CAMIAB
    Intervention Description
    This will be integrated CBT based motivational interviewing plus mindfulness based relapse prevention intervention group.
    Primary Outcome Measure Information:
    Title
    Feasibility measures
    Description
    Feasibility will be determined by recruitment rates, adherence rate and retention rates. The criterion for success of feasibility is to recruit >50% of eligible participants, adherence rate (number of home assignments completed; > 50%) and retention rate of 70%.
    Time Frame
    From baseline to 3rd month (at the end of intervention)
    Title
    Acceptability measure
    Description
    Acceptability will be determined based on the number of sessions attended by participants and success criterion for intervention acceptability is mean attendance rate of at least 8 sessions.
    Time Frame
    From baseline to 3rd month (at the end of intervention)
    Secondary Outcome Measure Information:
    Title
    The Maudsley Addiction Profile
    Description
    The Maudsley Addiction Profile is a brief, questionnaire that measures problems in four domains: substance use, health risk behaviour, physical and psychological health, and personal/social functions.
    Time Frame
    Change in problem scores from Baseline to 3rd Month and 6th month
    Title
    The Short Warwick-Edinburgh Mental Well-being Scale
    Description
    The Short Warwick-Edinburgh Mental Well-being Scale is a 7 items measure that will be used to measure mental wellbeing. It consists of 7 statements on a 5 point Likert scale. The minimum scale score is 7 and the maximum is 35. The high score indicates high mental wellbeing.
    Time Frame
    Change in scores from baseline to 3rd Month and 6th month
    Title
    EuroQol-5
    Description
    Quality of life will be measured using EuroQoL (EQ-5D) scale. This is a standardized instrument to measure health status and associated population utility weights. It measures five dimensions of health (mobility, self-care, usual activities, pain/ discomfort and anxiety/ depression) at different levels that include "no problems, slight problems, moderate problems, severe problems, and unable to do/extreme".
    Time Frame
    Change in scores from baseline to 3rd Month and 6th month
    Title
    Client service receipt inventory
    Description
    CSRI will be used to estimate the health and social services received.
    Time Frame
    Changes from baseline to 3rd Month and 6th month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria Participants with substance use disorder Meeting DSM-V criteria for substance use disorder Age 18 years and above Being able to understand spoken or written Urdu Have undergone through the process of detoxification before study intervention Exclusion Criteria • Any evidence of organic brain disease, clinically significant cooccurring medical illness or mental illness to the extent that can impede their ability to provide informed consent or engagement in the intervention.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Imran Bashir Chaudhry, Prof.
    Phone
    02135871845
    Email
    imran.chaudhry@pill.org.pk
    First Name & Middle Initial & Last Name or Official Title & Degree
    Muqaddas Asif, Ms.
    Phone
    04235775483
    Email
    muqaddas.asif@pill.org.pk
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Imran Bashir Chaudhry, Prof.
    Organizational Affiliation
    Pakistan Institute of Living and Learning
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Culturally Adapted Motivational Interviewing With CBT and Mindfulness Based Relapse Prevention for Substance Use Disorder in Pakistan (CAMIAB)

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