Data-driven rural wellness interventions for vitality and endurance (DRIVE) pilot

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The DRIVE pilot will implement data-driven, personalized lifestyle coaching in a rural outpatient context. It combines genomic, clinical, behavioral, and functional information to tailor wellness interventions. The study will evaluate feasibility, recruitment and engagement factors, and potential health improvements, informing future precision health research in similar communities. Outcomes include cardiometabolic, cognitive, mental health, and functional measures, collected over a four-month period. Key questions address data utility, biomarker relevance in rural populations, and scalable engagement frameworks.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adults \>18 years of age or older at enrollment ● Weight is greater than or equal to 110 lbs
* Able and willing to comprehend and sign the informed consent document
* Able and willing to perform required physical performance tests
* Able and willing to provide study samples
* Able and willing to participate in study procedures
* Able and willing to complete surveys, cognitive assessments, and questionnaires in English only
* Able and willing to wear a fitness tracker as continuously as possible for the duration of the study.

Weissman Hood Institute at Touro University Protocol # MRI010 Data-driven Rural Interventions for Vitality and Endurance (DRIVE) Pilot page 5 of 36

● Has or has ready access to a PC, tablet, or smartphone with an internet connection required for procedures that they consent to

Exclusion Criteria:

* A diagnosis of dementia
* Self-reported pregnancy or breastfeeding
* Individuals not fluent in written and spoken English
* Self-reported chronic or end-stage disease that would interfere with their participation in the study
* Severe and non-correctable hearing and visual impairment that would interfere with the ability to complete study measures
* Individuals for whom the total volume of blood would exceed 550 mL over an 8-week period and/or more than two draws within one week for combined clinical and research purposes. ● Any other vulnerable subject at the time of enrollment as specified above

Where it's running

• Weissman Hood Institute at Touro University
  Great Falls, Montana, United States Recruiting

Study contacts

• Study coordinator: Tiffany R Hensley-McBain, PhD
• Email: thmcbain@mclaughlinresearch.org
• Phone: 406-454-6016

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.