A Randomized Control Trial of Conversations Advancing Resilience and Empowerment (CARE) Intervention

Part of paid clinical trials in Edinburg, Texas.

Sponsor
University of Texas Rio Grande Valley
Study ID
NCT07698964
Status
Recruiting

Conditions

  • Blood Pressure Monitoring, Self
  • Health Promotion
  • Quality of Life

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 49 Years
Healthy Volunteers
Accepted

Interventions

  • Conversations Advancing Resilience and Empowerment (CARE) — BEHAVIORAL
    Health promotion intervention to address chronic disease risk

Study Details

The investigators propose to implement and evaluate the effectiveness of the peer-led CARE Intervention designed to mitigate health differences among rural and low-income communities in Texas. This intervention leverages the expertise of Community Health Workers (CHWs) to empower rural and low-income communities, improving health outcomes through outreach, education, counseling, and social support.

Key Dates

First listed
Jul 13, 2026
Start date
Jun 2, 2026
Status verified
Jul 2026
Primary completion
Jan 31, 2027
Completion
Mar 31, 2027

Study Design

Enrollment
200 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • Experimental: CARE Intervention Arm
    Participants will have up to 60 minute scripted health conversations with a Community Health Worker (CHW) across four visits to leverage opportunities during conversations to address flawed information and provide accurate information about quality of life, wellness, and mental health (Session #1); blood pressure (Session #2); nutrition (Session #3); and physical activity (Session #4).
  • No Intervention: CARE Control Arm
    Participants in the control group will receive no intervention, but will be invited to participate in the intervention (health education sessions) after the 6-month follow-up period has been completed.

Primary Outcome Measure

Health-related Quality of Life [ Time Frame: From Baseline, end of intervention (following completion of Health Education Session #4; the intervention was designed to last 4 weeks but may be extended due to scheduling considerations), 3 months post-intervention, 6 months post-intervention. ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
The University of Texas at Rio Grande ValleyEdinburgTexas78539
Lindsey Simon, Assistant Director Regulatory Clinical Research
9562968723
Moises Cisneros
9562712725
Candace A Robledo, PhD, MPH (PRINCIPAL_INVESTIGATOR)
CAN DO HoustonHoustonTexas77025
Jasmine J Opusunju, DrPH, MSEd
832-405-5451
Jasmine J Opusunju, DrPH, MSEd (PRINCIPAL_INVESTIGATOR)

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