A Family-centred Approach Enhancing Cardiovascular Health in Ugandan Adolescents and Their Families

NCT07265453 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1280

Last updated 2025-12-12

No results posted yet for this study

Summary

The FaCe-D Study, with funding from the Canadian Institute for Health Research (CIHR) through Global Alliance for Chronic Diseases (GACD) aims to adapt and implement an evidence-based family centred approach (FCA) to prevent cardiovascular diseases (CVD) among adolescents and their families. This 5-year implementation science study will be conducted in 16 villages in Jinja district and another 16 in Kampala beginning April 2024 to evaluate the effectiveness of FCA in reducing the risk of CVD in Uganda and to assess feasibility, adoption, while measuring the costs of implementation. The study will be implemented by a group of researchers from MRC/UVRI \& LSHTM, University of British Columbia (Canada), TASO (Uganda) and University of California San Francisco (UCSF) - USA with guidance from the Ministry of Health - Uganda.

Conditions

  • Adolescent Behavior
  • Lifestyle Modification
  • Cardiovascular Disease Other

Interventions

BEHAVIORAL

The immediate (treatment) arm, will receive the FaCe-D intervention comprising of 'HOME VISITS, DIET, PHYSICAL ACTIVITY AND HEALTH MESSAGING

The participants will receive the FaCe-D intervention comprising of dietary and exercise interventions delivered by Village Health Teams (VHTs)

OTHER

Control Arm - standard of care

Arm Description: They will continue to receive standard care with VHts performing their usual roles of health promotion for both communicable and non-communicable diseases as outlined by the Ministry of Health guidelines. This standard care involves visits by the VHT at least once a quarter to check hygiene and environment, children's immunisation status and other health promotion activities. The VHT may or may not involve the entire family/household.

Sponsors & Collaborators

  • University of California

    collaborator OTHER
  • The AIDS Support Organization

    collaborator OTHER
  • University of British Columbia

    collaborator OTHER
  • MRC/UVRI and LSHTM Uganda Research Unit

    lead OTHER

Principal Investigators

  • Prof Rachel King, PhD · University of California, San Francisco

  • Prof David Moore, PhD · University of British Columbia

  • Dr Josephine Birungi · MRC/UVRI and LSHTM Uganda Research Unit

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
10 Years
Max Age
19 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-07-05
Primary Completion
2027-01-31
Completion
2028-01-31

Countries

  • Uganda

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07265453 on ClinicalTrials.gov