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Health Impact 360: Advancing Physical, Social, and Mental Health Toward Cardiovascular Disease Prevention in Community Settings

University of Michigan · with National Heart, Lung, and Blood Institute (NHLBI), Detroit Hispanic Development Corporation · NCT07034352

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · All sexes
Healthy volunteers
Accepted
Study type
Interventional · Not applicable
Target enrollment
328
US sites recruiting
4
Study start
June 20, 2025
Record last updated
July 16, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

The purpose of this clinical trial is to evaluate an evidence-based intervention, Health Impact 360, toward the promotion of cardiovascular health (CVH), including physical, mental, and social health outcomes, among adults living in marginalized communities.

Study hypotheses include

  • Participants in the Health Impact 360 intervention arm will have better CVH (i.e., a higher overall LE8 score) at the 16-week endpoint compared to the control.
  • Participants in the Health Impact 360 intervention arm will report better mental health (i.e., a lower perceived stress score) at the 16-week endpoint compared to the control.
  • Participants in the Health Impact 360 intervention arm will report better social support and well-being (i.e., higher emotional support and instrumental support scores and reduced social isolation) at the 16-week endpoint compared to control.
  • Participants with greater intervention engagement (e.g., better session attendance) will experience greater intervention impacts across all primary and secondary outcomes relative to the minimally engaged peers.

Researchers will compare outcomes among intervention participants to outcomes among delayed intervention control participants who will be invited to participate in Health Impact 360 once all endpoint measures are collected.

Participants will

  • Engage in group-based programming twice per week for 8 weeks
  • Engage in group-based programming once per week for 8 weeks
  • Participate in survey-based and biometric data collection at two timepoints: baseline and 16-week endpoint
  • Self-monitor their physical activity via a study-provided pedometer

Being studied: Health Impact 360; Usual care - Wait list control

Conditions: Health Promotion; Cardiovascular Health

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

  • English or Spanish speaking
  • Able to participate in group-based programming

Exclusion Criteria

  • All pregnant persons to prevent pregnancy-related biometric changes from biasing outcome analyses

Recruiting US locations

  • Hasselbringe Senior Center

    Flint, MI 48504

    Site contact: Tarnesa Martin · 313-583-7088 · healthimpact360@umich.edu

  • Spirit of Victory

    Flint, MI 48504

    Site contact: Tarnesa Martin · 313-583-7088 · healthimpact360@umich.edu

  • Flint Development Center

    Flint, MI 48505

    Site contact: Latressa Gordon · 313-583-7088 · healthimpact360@umich.edu

  • RL Jones Community Center

    Flint, MI 48505

    Site contact: Latressa Gordon · 313-583-7088 · healthimpact360@umich.edu

Study contacts (from the official record)

  • Michelle Clayson · 734-763-2003 · mclayson@umich.edu
All mental health studies in Michigan →
Health Impact 360: Advancing Physical, Social, and Mental Health… (NCT07034352) | Bored Studies