Contextualization and Digitalization of WHO's Mental Health Action Gap Intervention Guide Substance Use Disorders Module

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorPakistan Institute of Living and Learning

About this trial

The aim of study is to:

1. To contextualize, adapt, customize and digitalize WHO's Mental Health Gap Action Programme Intervention Guide (e-mhGAP-IG); Substance Use Disorders Module (SUD module) V 2.0 for primary care settings (PCPs) in Pakistan. 2. To test the feasibility and acceotability of the e-mhGAP-IG (SUD module) training program in a feasibility cluster randomized controlled (cRCT) trial to enable mental health services in primary health care settings in Pakistan.

The proposed study includes contextualization, adaptation, customization, and a feasibility cRCT of e-mhGAP-IG (SUD module) V 2.0 by constituting a combination of traditional and technological approaches of eHealth (mHealth, blended learning, and telemedicine) enabling mental health services in primary care settings to be well informed and accessible. This intervention will empower 300 Primary Care Physicians (PCPs) based in Primary Care Units (PCUs) from urban settlements and Basic Health Units (BHUs) from rural settlements in three major cities, Karachi, Lahore, and Rawalpindi, Pakistan.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Primary and non-specialized healthcare providers working in the identified health facilities for this study across three targeted cities; willing to give informed consent for participation in this trial.

Disqualifiers

Any primary and non-specialized healthcare provider who is not permanently working in the selected health facilities, has no access to a smart mobile phone and/or internet connection; and is uncomfortable using a mobile phone.

Trial design

Design model

Parallel

Treatments tested in this trial

  • mhGap IG SUD Module Intervention Training

    Other intervention

    8 bi-weekly training sessions of e-mhGAP IG SUD Module

  • Control

    Other intervention

    Routine practices or standard of care

Treatment groups

300 Participants
are divided into 2 treatment groups
Group A: e-mhGAP-IG-SUD Intervention GroupExperimental treatment 1 intervention
Group B: Control GroupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility measures

Feasibility will be determined by recruitment and retention rates of participants throughout the study.

Time frame
From enrollement to the end of intervention at 4 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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Pakistan Institute of Living and Learning

Lead sponsor

Capaital University of Sceince of Technology

Collaborator