Recruiting

Engagement Strategies

Sponsor:

University of Colorado, Denver

Code:

NCT07569224

Conditions

Implementation Strategy Bundles for Structured Follow-up

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Providing reminder and resources via messages

Reminder and resources sent via navigation

Regular care

Study Details

Brief summary:

This study will evaluate the impact of 3 different strategies to increase engagement of participants in My Own Health Report (MOHR) and health behavior change activities over time. This study will evaluate the level of engagement, outcomes, cost and cost-effectiveness of these strategies.

Conditions

Implementation Strategy Bundles for Structured Follow-up

Study ID

NCT07569224

Start date

Jun 2, 2026

Status verified date

Jun, 2026

Completion date

Dec 31, 2029

Anticipated

Primary completion date

Jun 30, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

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)).

Study Design

Enrollment

1000 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

active comparator: Control Arm

Standardized version of usual care

experimental: R2 Message Only

Reminder and Resources Messages sent to patient

experimental: R2 Navigation only

Reminder and Resources provided to patient via health navigator

experimental: R2 Message + R2 Navigation

Both reminder and resources messages and navigation provided to the patient

Interventions

Providing reminder and resources via messages

Patients will be provided reminders and resources using messages sent to patients.

Reminder and resources sent via navigation

Patients will be provided reminders and resources using health navigators calling the patients.

Regular care

Regular (standard) care provided by healthcare provider team

Primary outcome measure

  • Number of MOHR risk factors [ Time Frame: From enrollment to the follow-up survey timepoint at 2 months. ]
  • REACH - specifically representative engagement [ Time Frame: From enrollment to the follow-up survey timepoint at 6 months. ]
  • Patient experience [ Time Frame: From enrollment to the follow up survey time point at 6 months. ]

Central Contacts and Locations

Central contacts

Locations

University of Colorado Hospital

Recruiting

Aurora, Colorado, United States, 80045

Contacts

Principal Investigator:

Amy Huebschmann

UCHealth Women's Integrated Services in Health (WISH)

Recruiting

Denver, Colorado, United States, 80045

Contacts

UCHealth Cherry Creek Medical Center

Recruiting

Denver, Colorado, United States, 80206

Contacts

Principal Investigator:

Amy Huebschmann

UCHealth Internal Medical Clinic - Lowry

Recruiting

Denver, Colorado, United States, 80230

Contacts

Principal Investigator:

Amy Huebschmann

UCHealth Lone Tree Medical Center

Recruiting

Lone Tree, Colorado, United States, 80124

Contacts

Principal Investigator:

Amy Huebschmann

UCHealth Family Medicine - Westminster

Recruiting

Westminster, Colorado, United States, 80021

Contacts

Principal Investigator:

Amy Huebschmann

More Information

Sponsor

University of Colorado, Denver

Last update posted

Jun 16, 2026

Last verified

Jun, 2026

Keywords

  • Implementation strategy
  • patient follow-up

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Colorado, Denver on 2026-06-16.