Clinical trial Recruiting at 2 sites Interventional Ages 40 to 85

Smartphone app program to help rural adults stick with exercise

Official title: Improving Exercise Adherence With App Technology for At-Risk Adults Living in Rural Kansas and Nebraska

Run by Creighton University · NCT07171255 · Data updated 2026-11-12

This project will try a smartphone app to help middle-aged and older adults in rural Kansas and Nebraska keep up with an exercise program aimed at lowering Alzheimer's and related dementia risk.

Quick facts

Study typeInterventional
Ages40 Years to 85 Years
SexAll
Enrollment54 (estimated)
SponsorCreighton University
Academic / other
Locations2 sites (Emporia, Kansas and 1 other locations)
StatusRecruiting
StartedAugust 22, 2025
Main results expectedJune 30, 2026
Study endsJune 30, 2026
Registry record updatedSeptember 12, 2025
Trial IDNCT07171255 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are 40–85 years old, underactive, live in rural Kansas or Nebraska by RUCA codes, can use a smartphone, speak English, and have no major cognitive impairment or medical contraindication to exercise.

Probably not a fit

Patients with significant cognitive impairment, contraindications to high-intensity exercise, recent orthopedic surgery, no smartphone access, or who do not live in the designated rural areas are unlikely to benefit from this program.

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

What this trial studies

The program delivers RemoteEx+ through a smartphone application that provides video demonstrations, structured workout plans, motivational messages, and weekly dementia-risk reduction education. The study uses a pre/post design to measure exercise adherence, self-efficacy for exercise, enjoyment, and quality of life before and after the intervention. Participants are 40–85 years old, underactive, live in rural areas by RUCA codes, own a smartphone, and must not have significant cognitive impairment or contraindications to high-intensity exercise. Enrollment is coordinated through Emporia State University (Kansas) and Creighton University (Nebraska) while the intervention is delivered remotely.

Why it matters

Potential benefit: If successful, the app could increase regular exercise among rural adults and potentially lower their risk of cognitive decline while improving well-being.

How similar studies have gone: Previous smartphone and remotely delivered exercise programs have shown modest improvements in activity levels and self-efficacy, but applying a tailored RemoteEx+ app to rural adults at elevated dementia risk is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 40-85 years
* Characterized as underactive by the Telephone Assessment of Physical Activity (TAPA)50
* Self-reported proficiency in English
* Own a smartphone and willing to download an application
* Primary care provider clearance to participate for those who do not pass the PAR-Q+51
* Live in a rural area (Rural-Urban Commuting Area \[RUCA\] Codes) 52

Exclusion Criteria:

* Contraindications to high-intensity exercise
* Cognitive impairment (\<19 on the Telephone Montreal Cognitive Assessment \[MoCA\])
* Neurodegenerative or acute neurological diagnoses (e.g., Parkinson's disease, stroke, traumatic brain injury)
* Orthopedic surgery or injuries in the last 6 months

Where it's running

  • Emporia State University
    Emporia, Kansas, United States
    Recruiting
  • Creighton University
    Omaha, Nebraska, United States
    Recruiting

Study contacts

Similar studies

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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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.