Clinical trial Recruiting at 1 site Interventional Ages 20 and up

Community participatory groups to prevent and control Type II diabetes in rural Peshawar and Swabi

Official title: Engagement of coMmunity Through Participatory Learning and Action for cOntrol and preVEntion of Type II Diabetes and Its Risk Factors [EMPOWER-D]: Cluster Randomized Controlled Trial

Run by Khyber Medical University Peshawar · NCT06561126 · Data updated 2026-11-12

This project will try a community group-based Participatory Learning and Action program to help prevent and control Type II diabetes among adults living in rural Peshawar and Swabi, Pakistan.

More Type II Diabetes Mellitus trials

Quick facts

Study typeInterventional
Ages20 Years and up
SexAll
Enrollment12744 (estimated)
SponsorKhyber Medical University Peshawar
Academic / other
Locations1 site (Peshawar, KPK)
StatusRecruiting
StartedMay 1, 2025
Main results expectedMay 30, 2026
Study endsAugust 31, 2026
Registry record updatedSeptember 2, 2025
Trial IDNCT06561126 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 20 years and older who live in the rural areas of Peshawar or Swabi, are willing to consent, and can attend scheduled community group meetings are ideal candidates.

Probably not a fit

People who cannot attend or participate in regular group activities, have severe health conditions that prevent active involvement, or require intensive medical management rather than community support may not benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The trial adapts a Participatory Learning and Action (PLA) approach—using community groups that follow cycles of problem identification, collaborative planning, action, and participatory evaluation—to address Type II diabetes and intermediate hyperglycemia. It will be delivered in rural clusters in Peshawar and Swabi and tailored to local needs, using methods such as photo-voice, group discussion, and role-play. A cluster randomized controlled design will compare PLA intervention clusters to control clusters to measure impact on diabetes prevention and control outcomes. Adults aged 20 and over across the glycemic spectrum (normoglycemia, pre-diabetes, and diabetes) will be invited to participate and attend regular local group meetings.

Why it matters

Potential benefit: If successful, the program could reduce new diabetes cases and improve self-care and prevention behaviors by empowering local communities to adopt healthier practices.

How similar studies have gone: PLA approaches have demonstrated effectiveness for maternal and neonatal health in South Asia and informed diabetes-focused community programs such as D-Magic Bangladesh, providing precedent though community PLA for diabetes control remains less widely validated.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Individuals aged 20 years and above.
* Participants residing in the rural areas of Peshawar and Swabi, Pakistan.
* Individuals willing to participate in the study and provide consent.
* Both individuals with normoglycemia, intermediate hyperglycemia, and diabetes are encouraged to participate.
* Participants who can attend the scheduled meetings and interventions as per the study protocol.

Exclusion Criteria:

* Individuals below the age of 20 years.
* Individuals unwilling to provide consent for participation.
* Participants with severe health conditions that may hinder their active involvement in the study.
* Individuals with a history of non-compliance with medical interventions or research protocols

Where it's running

  • Khyber Medical University Peshawar
    Peshawar, Kpk, Pakistan
    Recruiting

Study contacts

  • Principal investigator: Prof. Dr Zia Ul Haq, MBBS,MPH,PhD — Khyber Medical Univeristy Peshawar
  • Study coordinator: Prof. Dr Zia Ul Haq, MBBS,MPH,PhD
  • Email: drzia@kmu.edu.pk
  • Phone: +92 333 9258763

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.