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Study identifier: NCT07034352 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: RecruitingHI360

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

Condition: Health Promotion · Cardiovascular Health  ·  Sponsor: University of Michigan

PhaseNA
Planned participants328
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYesCheck eligibility criteria ↓
Where7 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

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…

This description comes directly from the study's public registry record.

Talk to the study team

Michelle Clayson  ·  734-763-2003  ·  mclayson@umich.edu

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (7)

Community Health and Social Service Centers (CHASS)Detroit, Michigan, United StatesCompleted
Eastside Community Network (ECN)Detroit, Michigan, United StatesCompleted
Detroit Hispanic Development Corporation (DHDC)Detroit, Michigan, United StatesCompleted
Hasselbringe Senior CenterFlint, Michigan, United StatesRecruiting
Spirit of VictoryFlint, Michigan, United StatesRecruiting
Flint Development CenterFlint, Michigan, United StatesRecruiting
RL Jones Community CenterFlint, Michigan, United StatesRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

FlintDetroit

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