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NCT Number: NCT07463144

Evaluation of a Mobile Wellness Application and Wearable Fitness Tracker on Weight Management and Health Outcomes

This randomized controlled trial aims to evaluate the effectiveness of a mobile wellness application, both alone and in combination with a wearable fitness tracker, for supporting weight management, physical activity, and mental well-being. Adults with a body mass index (BMI) ≥25 will be randomized to one of three groups: (1) mobile wellness application + wearable tracker, (2) mobile wellness application only, or (3) control receiving standard health information. Participants will use the interventions over a 12-week period, and outcomes including weight change, activity levels, and self-reported mental health will be assessed.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Sterling Institutional Review Board - Remote/Virtual Participation Only

Atlanta, Georgia, 30328, United States

About this study

Obesity is a growing public health concern worldwide, contributing to chronic conditions such as type 2 diabetes, cardiovascular disease, and mental health challenges. Digital wellness interventions, including mobile apps and wearable devices, have the potential to support behavior change, physical activity, and weight management.

This study will examine whether adding a wearable fitness tracker to a mobile wellness application enhances health outcomes compared with app-only use or standard health information. The trial is decentralized, conducted remotely, and does not require in-person visits.

Participants will complete baseline assessments, be randomized into one of three study arms, and follow a structured program for 12 weeks. Self-reported surveys, weight measurements (with optional video verification), app usage data, and wearable-collected data (for the tracker group) will be used to evaluate outcomes.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age: 18+ years
  • A baseline BMI ≥ 25
  • Willing to use the BetterMe mobile wellness app and fitness tracker for the entirety of the study
  • Ownership of a smartphone
  • Currently inactive, as defined by acknowledging "several times a month" or "never" to the exercise frequency question in the screener
  • Acknowledging "I believe I can do it" or "I'm uncertain, but willing to try" to the confidence to succeed question in the screener
  • Willingness to use scales for body weighing and submit video recording

Exclusion criteria

  • A baseline BMI < 25
  • Pregnant or planning to become pregnant
  • Breast-feeding or less than 6 months postpartum
  • Currently diagnosed with insomnia, sleep apnea, or other clinical sleep disorder
  • Diagnosed thyroid, liver, kidney, cardiovascular, moderate-severe depression or anxiety, bipolar disorder, schizophrenia, or cancer-related disease
  • Recent significant weight loss (e.g., >5-10% in the last 6 months)
  • Extreme life circumstances (e.g. family illness, recently lost job, going through a divorce)
  • Cannot participate in a regular exercise routine for any reason during the course of the study (i.e. contraindications to exercise)
  • Used the same mobile wellness app and/or fitness tracker in the last year
  • Currently enrolled in an additional weight loss program (e.g. Noom, WW, health coaching) and/or working with a dietician
  • Current, previous (in the last 6 months), or planned use of weight loss medications (e.g., Ozempic, Wegovy, etc.) (in the next 6 months)

Treatment and study plan

App + Fitness Tracker

Behavioral

Participants will use a commercially available mobile wellness app alongside a wearable fitness tracker. The app provides personalized exercise programs, habit tracking, progress monitoring, and motivational support. The wearable collects daily steps, heart rate, heart rate variability, and sleep metrics to enhance personalized feedback. Participants are encouraged to engage with both tools daily over a 12-week period to support weight management, physical activity, and overall well-being.

App Only

Behavioral

Participants will use the same mobile wellness app without the wearable fitness tracker. The app delivers personalized exercise programs, habit tracking, progress monitoring, and motivational support. Participants are encouraged to use the app daily over 12 weeks to support weight management, physical activity, and overall well-being.

Control Group

Behavioral

Participants will continue their usual health and exercise routines without access to the app or wearable tracker. They will receive standard wellness information via email or blog posts over the 12-week study period. This group serves as a comparison to evaluate the effects of the interventions on weight management, physical activity, and well-being.

Primary outcomes

  1. Weight Change

    Time frame: 3 months

    Change in % body weight

Secondary outcomes

  1. Physical Activity

    Time frame: 3 months

    Physical activity levels (self-reported via IPAQ (International Physical Activity Questionnaire) and wearable devices.

    Scale: IPAQ score ranges from 0 to 1000+ MET-minutes/week (where higher scores indicate higher activity levels).

    Wearable Tracking: Data from wearable devices will be summarized in minutes of activity per week.

  2. Mental Health: Total Anxiety Score

    Time frame: 3 months

    Measured by the Generalized Anxiety Disorder 7-item scale (GAD-7). The GAD-7 is a 7-item self-report questionnaire used to assess the severity of generalized anxiety disorder. Each item is scored from 0 (not at all) to 3 (nearly every day). The total score is calculated by summing the scores of all 7 items, resulting in a single value ranging from 0 to 21. Higher scores indicate greater anxiety severity.

  3. Mental Health: Depression Total Score

    Time frame: 3 months

    Measured using the Patient Health Questionnaire-8 (PHQ-8). The PHQ-8 is an 8-item self-report instrument used to measure the severity of depressive symptoms. Each item is scored on a 4-point scale ranging from 0 (not at all) to 3 (nearly every day). The total score is calculated by summing the scores of all 8 items, resulting in a single value ranging from 0 to 24. Higher scores indicate greater severity of depressive symptoms.

  4. Health-Related Quality of Life

    Time frame: 3 months

    Short Form 12 (SF-12), Health-Related Quality of Life Scale

    Scale: Scores range from 0 to 100 (where higher scores indicate better health-related quality of life).

  5. App usage metrics: Time

    Time frame: 3 months

    Metric: Time spent in app (minutes)

  6. App usage metrics: Exercise Count

    Time frame: 3 months

    Metric: Exercises started/completed (count)

  7. App usage metrics: Frequency

    Time frame: 3 months

    Metric: Frequency of logging (number of logins).

Sponsors and collaborators

Lead sponsor

BetterMe Limited

Industry

Registry information

Official study title

Evaluation of App-only Users Compared With Wearable Band + App Users With Regard to Weight Management and Program Engagement on the BetterMe Platform

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 11, 2026
Registry last updated
Mar 11, 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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