MOHR follow-up support options to boost healthy habits
Testing the Impact of the My Own Health Report Intervention With 3 Distinct Options for Structured Follow-up as Compared to a Control Condition
This study will test three follow-up approaches (electronic reminders and resources, navigator-delivered reminders and resources, or regular care) to see if they help adults with low physical activity and low fruit/vegetable intake stay engaged with MOHR and improve health behaviors.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Colorado, Denver Academic / other |
| Locations | 6 sites (Aurora, Colorado and 5 other locations) |
| Trial ID | NCT07569224 on ClinicalTrials.gov |
What this trial studies
In a randomized comparative effectiveness-implementation trial, 1,000 adults who completed the MOHR health risk assessment and have both low physical activity and low fruit/vegetable intake will be enrolled. Participants will be randomized to receive Reminder-and-Resources messages (R2 Message), person-delivered Reminder-and-Resources navigation (R2 Navigation), or usual care and followed for engagement, behavior change, and cost outcomes. The intervention menus for MOHR delivery and the R2 bundles were co-developed with clinic partners and patient advisors and are delivered electronically or by staff. The study will measure levels of engagement, behavioral outcomes, and cost-effectiveness across the three strategies.
Who should consider this trial
Good fit: Adults aged 18 or older who completed the MOHR assessment, score at-risk for both physical activity (<150 minutes/week) and diet (<5 servings/day of fruits/vegetables), and receive care at a participating clinic are the best candidates.
Not a fit: Patients who did not complete the MOHR assessment, who have advanced illness or cognitive impairment, who speak neither English nor Spanish, or who do not attend the participating Colorado clinics are unlikely to benefit from participating.
Why it matters
Potential benefit: If successful, one of the follow-up approaches could help patients maintain activity and dietary goals more consistently by improving ongoing engagement with MOHR.
How similar studies have performed: Prior MOHR pilot work showed significant improvements in physical activity and diet, but structured follow-up bundles like R2 Message versus R2 Navigation are less tested and represent a newer implementation comparison.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults, aged 18 years and older. * Completion of the MOHR health risk assessment and goal-setting tool * Score in the "at-risk" range on both of the following cancer risk assessments: 1) Physical activity risk: less than 150 minutes per week of moderate to vigorous physical activity; Diet risk: Less than 5 servings daily of combined fruit/vegetables * Patient at one of the participating clinics Exclusion Criteria: * Incomplete or no MOHR assessment * Language preference/proficiency other than English or Spanish * Presence of a condition(s) or diagnosis, either physical or psychological, or physical exam finding that precludes participation. Examples include - Indices of advanced illness and frailty, such as dementia (ICD-10 codes F01.50, F01.51, F02.80, F02.81, F03.90, F03.91, F10.27, F10.97, G31.09, G31.83 or dementia medication of Donepezil • Galantamine • Rivastigmine, Memantine, or Donepezil-memantine)).
Where this trial is running
Aurora, Colorado and 5 other locations
- University of Colorado Hospital — Aurora, Colorado, United States (Recruiting)
- UCHealth Women's Integrated Services in Health (WISH) — Denver, Colorado, United States (Recruiting)
- UCHealth Cherry Creek Medical Center — Denver, Colorado, United States (Recruiting)
- UCHealth Internal Medical Clinic - Lowry — Denver, Colorado, United States (Recruiting)
- UCHealth Lone Tree Medical Center — Lone Tree, Colorado, United States (Recruiting)
- UCHealth Family Medicine - Westminster — Westminster, Colorado, United States (Recruiting)
Study contacts
- Study coordinator: Principal Investigator
- Email: amy.huebschmann@cuanschutz.edu
- Phone: (303) 724-2268
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.