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Recruiting NCT06730737

NCT06730737 Lifewise Preventive Video Education in Primary Care

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Clinical Trial Summary
NCT ID NCT06730737
Status Recruiting
Phase —
Sponsor Trinity Health-Livonia
Condition Prevention Harmful Effects
Study Type INTERVENTIONAL
Enrollment 350 participants
Start Date 2025-04-01
Primary Completion 2028-01-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 80 Years
Study Type INTERVENTIONAL
Interventions
Video preventive education

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 350 participants in total. It began in 2025-04-01 with a primary completion date of 2028-01-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

It is widely accepted that prevention is far more impactful than curative medicine and must be included in primary care. In a previous pilot study, we evaluated passive video preventive lifestyle education in the emergency department. The current study is a randomized prospective trial assessing the practicality and impact of a brief interactive educational video intervention to patients during primary care clinic visits.

Eligibility Criteria

Inclusion Criteria: * Adults between the ages of 18 and 80, inclusive. Exclusion Criteria: * Non-English-speaking patient * Unable or unwilling to consent to the study * Unable or unwilling to hear a video on a smartphone or computer tablet * The patient is in hospice care * Patients with advanced dementia, in the opinion of the person administering the survey

Contact & Investigator

Central Contact

Daniel Keyes, MD, MPH

✉ dankeyes@msu.edu

📞 734-931-0734

Principal Investigator

Daniel Keyes, MD, MPH

PRINCIPAL INVESTIGATOR

Trinity Health-Livonia

Frequently Asked Questions

Who can join the NCT06730737 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 80 Years, studying Prevention Harmful Effects. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06730737 currently recruiting?

Yes, NCT06730737 is actively recruiting participants. Contact the research team at dankeyes@msu.edu for enrollment information.

Where is the NCT06730737 trial being conducted?

This trial is being conducted at Livonia, United States.

Who is sponsoring the NCT06730737 clinical trial?

NCT06730737 is sponsored by Trinity Health-Livonia. The principal investigator is Daniel Keyes, MD, MPH at Trinity Health-Livonia. The trial plans to enroll 350 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology