Testing Support Strategies for My Own Health Report (MOHR)

This study is looking at different ways to help people use the My Own Health Report (MOHR) program and make healthy changes. We are testing three approaches: sending reminders and resources through messages, having health navigators call patients with reminders and resources, or providing regular care. We want to see how well these strategies help people stay involved, improve their health, and how much they cost. You might be able to join if you are an adult aged 18 or older, have completed the MOHR health assessment, and score "at-risk" for physical activity (less than 150 minutes per week) and diet (less than 5 servings of fruits/vegetables daily). We will measure how many MOHR risk factors you have at 2 months, how engaged you are at 6 months, and your overall experience at 6 months. The current recruitment status is unclear.

Study design
This is an interventional study, meaning participants will receive one of the three support strategies. The planned enrollment is 1000 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for up to 6 months after enrollment to measure outcomes.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07569224

Testing the Impact of the MOHR Follow-up Support

Recruiting
NAAges 18+InterventionalPrevention
University of Colorado, Denver
~1,000 participants
Updated 2026-06-16 on ClinicalTrials.gov
What's tested:Providing reminder and resources via messagesReminder and resources sent via navigationRegular care

At a glance

Recruiting sites
6 of 6 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of MOHR risk factors
Measured over From enrollment to the follow-up survey timepoint at 2 months.
+2 more outcomes measured
Implementation Strategy Bundles for Structured Follow-up
6 sites across 1 states
Colorado6

Opens a ready-to-send draft in your own email app — review before sending.

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

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

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)).
  • Number of MOHR risk factorsFrom enrollment to the follow-up survey timepoint at 2 months.

    Primary effectiveness outcome measured on scale from -6 to +6 as change of the number of risk factors improved. MOHR questions are organized into 6 risk areas: 1) intake of fruits and vegetables; 2) high sugar beverages; 3) fast food; 4) physical activity; 5) stress; and 6) sleep. Each risk factor is evaluated as low risk, medium risk, or high risk. Level of improvement in risk factors outcome will be a count score from -6 to 6 (any improvement or decrement in level of risk in each factor will count as 1 or -1).

  • REACH - specifically representative engagementFrom enrollment to the follow-up survey timepoint at 6 months.

    Primary implementation outcome. Representative engagement: Engagement during the follow-up period involves interactions over time of the participant with either or both a navigator or text messages . Engagement will be assessed percent of navigator calls completed (maximum of 12 over 6 months) and percent of text messages successfully sent (maximum of 60 over 6 months). To assess whether engagement is representative our primary assessments will be if there is differential engagement across conditions (e.g., an interaction effect) based on 1) number of baseline social needs, 2) Latine vs. non Latine ethnicity or 3) digital literacy.

  • Patient experienceFrom enrollment to the follow up survey time point at 6 months.

    Primary practice value outcome measured by change in mean score on Patient Assessment of Quality-of-Care subscales of goal setting/tailoring and follow-up/coordination (PACIC). Scale ranges from almost never (indicating the worst patient experience) to almost always (indicating the best patient experience).