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NCT Number: NCT07313540

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

The objective of this project is to test the feasibility of using a smartphone app in a community setting through collaborating with community-based organizations. The app is called utmbHealthyBrain and it has three activities: (1) drawing, (2) Tai-Chi and meditation, and (3) prayer reading. It also has a "share" function to enable users to interact with their family and friend. These activities can be translated to humans' well-beings such as a more stable emotion, more muscle movement, and better social engagement. This app does not collect any personal data and users are not required to register an account either. The overall study period is 6 weeks including one introduction session (week 1), four weeks of intervention (week 2 to 5), and final feedback session (week 6).

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Key information

Age range

50 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Texas Medical Branch, Galveston

Galveston, Texas, 77555, United States

Location contact

Wei-Chen Lee, PhD

CONTACT

[email protected]

409-747-2649

About this study

This study will conduct primary data collection on 20 individuals aged 50+ and another 20 who are their caregivers regarding the use of a smartphone application (app) to promote mental well-being. The aging population is growing rapidly from 52 million in 2018 to 95 million by 2060. Approximately 34.2 million Americans have provided unpaid care to an adult age 50 or older. While 82% of them care for one adult, about 15% care for 2 adults and 3% for 3 or more adults. This number is expected to increase as the population ages. Deteriorating health of care recipients and caregivers is a critical issue that may be delayed by the use of a smartphone app to improve mental and emotional well-beings.

The objective of this proposed project is through collaborating with community-based organizations to test the acceptability and feasibility of a smartphone app intervention. We will collaborate with the community-based organization (i.e., UTMB OLLI and Libbie's Place) to announce the study by flyers and request RSVP to the study investigator. The investigator will provide instructions on using the smartphone app to potential participants and obtain participant's written consent to the study. After consenting, 20 pairs of older adults and their caregivers will fill out a mood test, download the app to their phone, and use it at least three times a week for four weeks. Participants will be required to keep their utilization log and fill out the post-intervention mood test and the feedback survey after four weeks of participation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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)
  • People who are at hospice care
  • 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)

Treatment and study plan

utmbHealthyBrain Smartphone App

Behavioral

a wellness product related to relaxation and stress management and presents a low risk to the safety of users and other persons

Primary outcomes

  1. Feasibility of a smartphone app intervention

    Time frame: 3 times per week for 4 weeks

    Feasibility will be assessed by participant adherence to the smartphone app intervention, defined as completion of activities three times per week.

Study contacts

Contact information is provided by the study sponsor or research team.

Wei-Chen Lee, PhD

CONTACT

[email protected]

409-747-2649

Sponsors and collaborators

Lead sponsor

The University of Texas Medical Branch, Galveston

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jan 2, 2026
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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