Actively Recruiting

Phase Not Applicable
Age: 20Years +
All Genders
Healthy Volunteers
ID07350694

Engagement of coMmunity Through Participatory Learning and Action for cOntrol and preVEntion of Type II Diabetes and Its Risk Factors [EMPOWER-D-Afg]: Feasibility Trial in Rural Kabul-Afghanistan

Led by HealthNet Transcultural Psychosocial Organization · Updated on 2026-01-20

250

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

Sponsors

H

HealthNet Transcultural Psychosocial Organization

Lead Sponsor

U

University of York

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a Participatory Learning and Action (PLA) based intervention aimed at preventing and controlling Type II Diabetes Mellitus (TIIDM) in rural Kabul, Afghanistan. TIIDM is a growing global health emergency, especially in low- and middle-income countries like Afghanistan, where many cases remain undiagnosed. This study aims to adapt and test a culturally appropriate intervention based on evidence from a successful trial in Bangladesh, focusing on the unique social and health challenges in rural Afghan communities. The study involves two groups: one receiving the PLA intervention through group sessions lasting about 2 to 3 hours, designed to engage community members with TIIDM and improve diabetes-related outcomes; and a control group receiving usual care and information about the project but no PLA sessions. Participants in the intervention group will be evaluated 10 months after starting the sessions to assess feasibility and outcomes. Participants will be involved in scheduled meetings and assessments before, during, and after the intervention, using structured and validated checklists to measure feasibility, acceptability, and implementation factors of the PLA approach. The study will also monitor the frequency of Type 2 Diabetes and intermediate hyperglycaemia over 12 months. Overall participation may last up to 12 months, with ongoing evaluation of barriers and facilitators to implementing the intervention in the community.

CONDITIONS

Brief Title

Engagement of coMmunity Through Participatory Learning and Action for cOntrol and preVEntion of Type II Diabetes and Its Risk Factors

Who Can Participate

Age: 20Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 20 years and above for the intervention phase
  • Individuals aged 30 years and above for baseline and endline assessments
  • Residents of randomized clusters in Kabul, Afghanistan
  • Willingness to participate and provide consent
  • Includes individuals with normal blood sugar, intermediate hyperglycaemia, and diabetes
  • Ability to attend scheduled meetings and interventions as per protocol
Not Eligible

You will not qualify if you...

  • Individuals below 20 years for the intervention phase
  • Individuals below 30 years for baseline and endline assessments
  • Unwillingness to provide consent
  • Health conditions hindering active involvement in the study
  • Non-compliance with research protocols

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - Approximately 10 months

Participants in the intervention group attend Participatory Learning and Action (PLA) sessions lasting approximately 2 to 3 hours each to educate and engage the community for prevention and control of Type II Diabetes.

Group sessions lasting 2 to 3 hours each; frequency as per community schedule

Follow-up

Duration - Up to 2 months after intervention completion

Participants are evaluated using a structured, validated assessment checklist to test feasibility, acceptability, and outcomes of the PLA intervention.

1 to 2 visits for endline assessments

Trial Site Locations

Total: 1 location

1

HealthNet TPO, Afghanistan

Kabul, Kabul, Afghanistan, 24000

Actively Recruiting

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Research Team

A

Abdul Rahman Shahab, MPH

S

Sayed Murtaza Sadat Hofiani, MPH

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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