AI-powered personalized exercise plan for older adults using a wearable app
Official title: Artificial Intelligence-based Personalized Exercise Prescription Through Mobile Health on Physical Activity and Health Outcomes in Older Adults: A Feasibility Study
Run by The University of Tennessee, Knoxville · NCT07768670 · Data updated 2026-11-12
A wearable-enabled, AI-driven exercise app is tested to see if it’s feasible and acceptable for adults 65+ and whether it can help increase activity, improve mood, and boost quality of life.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 65 Years and up |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | The University of Tennessee, Knoxville Academic / other |
| Locations | 1 site (Knoxville, Tennessee) |
| Status | Recruiting |
| Started | October 1, 2026 |
| Main results expected | December 20, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | August 20, 2026 |
| Trial ID | NCT07768670 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 65 and older who own a compatible smartphone, have internet access, can use a smartphone app, and can safely engage in physical activity.
✕Probably not a fit
Older adults who are unable to use smartphone technology, lack internet access, or cannot safely participate in physical activity may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This feasibility study tests a mobile health solution that uses AI to tailor exercise prescriptions for older adults, delivered through a wearable device and fitness app. It evaluates feasibility, acceptability, appropriateness, and preliminary efficacy on physical activity, mental health, and quality of life. The study follows a stage 1b NIH framework, focusing on implementation processes, user engagement, and potential signals of benefit. Eligible participants are adults 65 and older who own a smartphone, have internet access, and can safely participate in physical activity. Outcomes will inform refinement of the AI-based intervention before larger trials.
Why it matters
Potential benefit: If successful, the approach could help more older adults increase activity and improve well-being through a personalized, technology-driven program.
How similar studies have gone: Previous studies have shown that mobile health and wearable interventions can increase activity levels, but AI-driven SDT- and BCT-based personalization in older adults is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Be aged 65 years or older. * Own a smartphone (Android or iOS) compatible with study applications. * Have reliable access to the internet or Wi-Fi. * Demonstrate basic digital literacy sufficient to operate a smartphone (e.g., ability to open applications, navigate simple interfaces, and follow on-screen instructions), with or without initial guidance from the research staff. * Be able to safely engage in physical activity, as determined by the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) or physician approval if indicated. * Report engaging in less than 150 minutes of moderate-to-vigorous physical activity (MVPA) per week. * Be able to communicate in English sufficiently to complete study procedures and assessments. Exclusion Criteria: * Are younger than 65 years of age. * Do not own a compatible smartphone (Android or iOS) or do not have reliable internet/Wi-Fi access. * Are deemed unable to safely participate in physical activity based on the screening process (including PAR-Q+, STEADI, and research staff assessment), or do not obtain required physician clearance when indicated. * Currently meet or exceed 150 minutes of moderate-to-vigorous physical activity (MVPA) per week. * Are unable to communicate in English sufficiently to understand study procedures, provide informed consent, or complete study-related assessments. * Have any medical, physical, or cognitive condition that, in the judgment of the research team, would make participation unsafe or prevent completion of study procedures.
Where it's running
-
Kinesiology, Recreation, and Sport Studies (865) 974-3340 krss@utk.edu
Knoxville, Tennessee, United States Recruiting
Study contacts
- Principal investigator: Zan Gao, PhD — University Of Tennessee,knoxville
- Study coordinator: John Oginni, MS
- Email: pael@utk.edu
- Phone: 8659747971
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Single-session intervention to change ambiguity aversion
This trial tests whether one brief intervention can change how adults with intolerance of uncertainty and anxiety make ambiguous decisions and how their brains respond.
-
See if preoperative anxiety affects recovery after major digestive cancer surgery
This study tests whether anxiety before surgery is linked to more complications after major digestive cancer operations in French-speaking adults.
-
Mindful Smartphone Use: A Mindfulness-Based Program for Teens with Sleep and Mood Challenges
This study tests Mindwire, a mindfulness-based program, to see if it helps teens with problematic phone use who also have depression or anxiety.
-
Tele-based wellbeing centres for women's mental health in Bangladesh
A randomized trial tests whether tele-counselling for depression and anxiety in Bangladeshi women is as effective as in-person counselling.
-
Buzzy Bee for Pain and Anxiety Control During Pediatric Dental Local Anesthesia
This study tests whether the Buzzy Bee device, with cold and vibration, reduces pain and anxiety during a dental injection in kids aged 5-7 compared with standard distraction.
-
Reflexology and hand massage after cesarean section
This study tests whether reflexology hand massage or stroking hand massage can reduce anxiety and increase satisfaction, and how they affect heart/blood pressure after cesarean delivery.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.