Clinical trial Recruiting at 1 site Interventional Ages 50 to 100

Feasibility of a Smartphone App to Support Mental Well-Being for Older Adults and Caregivers

Official title: Feasibility of A Smartphone Application Intervention in Community Settings: A Pretest-Posttest Pilot Study

Run by The University of Texas Medical Branch, Galveston · NCT07313540 · Data updated 2026-11-12

This pilot test checks whether the utmbHealthyBrain app can be used in community settings by adults 50+ and their caregivers to support mood and social connection over six weeks.

Quick facts

Study typeInterventional
Ages50 Years to 100 Years
SexAll
Enrollment40 (estimated)
SponsorThe University of Texas Medical Branch, Galveston
Academic / other
Locations1 site (Galveston, Texas)
StatusRecruiting
StartedOctober 22, 2026
Main results expectedOctober 2027
Study endsOctober 2027
Registry record updatedNovember 5, 2026
Trial IDNCT07313540 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 50 and older and their caregivers who can commit to six weeks, can read and communicate in English, and own a smartphone.

Probably not a fit

Individuals with moderate to severe cognitive impairment or psychiatric disorders, or those not planning to stay in the area, may not benefit.

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

What this trial studies

This pilot study will enroll 20 older adults and 20 caregiver pairs to use the utmbHealthyBrain smartphone app for six weeks in collaboration with community organizations. Participants will complete a mood assessment, install and use the app at least three times per week, and maintain a usage log, followed by a post-intervention mood check and feedback survey. The app includes drawing, Tai-Chi and meditation, and prayer readings, plus a share feature for family interaction, with no required account creation or collection of personal data. The study aims to assess feasibility and acceptability of delivering a smartphone-based mental-well-being intervention in real-world community settings. Eligible dyads include English-speaking pairs where both members have a smartphone and can participate fully for six weeks.

Why it matters

Potential benefit: If feasible and acceptable, this approach could offer a scalable way to support mood, social engagement, and daily activity among older adults and their caregivers.

How similar studies have gone: Previous similar app-based interventions in aging populations have shown feasibility and positive user engagement, though this exact multi-component app in community settings is novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Individuals aged 50+ who has a primary source of assistance (no age limitation for the caregiver)
2. Both care recipient and caregiver can participate in the study for six weeks in total,
3. Both care recipient and caregiver can read, listen, write, and speak English
4. Both care recipient and caregiver have a personal smartphone.

Exclusion Criteria:

1. People who are diagnosed with any middle to severe cognitive symptoms (dementia or Alzheimer's Disease) or any psychiatric disease (depression, bipolar, PTSD, Schizophrenia, anxiety disorders, eating disorders)
2. People who are at hospice care
3. People who plan to move out of the current area in one year, and (4) people younger than 50 (but no age limitation for caregivers)

Where it's running

  • University of Texas Medical Branch, Galveston
    Galveston, Texas, United States
    Recruiting

Study contacts

  • Principal investigator: Wei-Chen Lee, PhD — University of Texas Medical Branch, Galveston
  • Study coordinator: Wei-Chen Lee, PhD
  • Email: weilee@utmb.edu
  • Phone: 409-747-2649

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.