- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05621044
Physical Activity Smartphone App for African American Men (FitBros) Ph II
Smartphone App to Increase and Maintain Physical Activity in African American Men (FitBrothers) Phase II
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
Colorado
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Golden, Colorado, United States, 80401
- Klein Buendel, Inc.
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-
District of Columbia
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Washington D.C., District of Columbia, United States, 20057
- Georgetown University
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Louisiana
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Baton Rouge, Louisiana, United States, 70808
- Pennington Biomedical Research Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Comparative Effectiveness Trial (CET) Inclusion criteria:
- self-identified African American male
- at least 30 years of age
- BMI > 18.5 kg/m2 and < 45 kg/m2
- resting systolic blood pressure # 159 mmHg and a diastolic blood pressure # 99 (to reduce risk of exercise-induced cardiovascular events)
- free of significant medical problems that would impact their ability to engage in aerobic and/or resistance training
- owns a smartphone
- sedentary at baseline (not being physically active ≥3 d·wk-1 for 20 min each time for the previous 6 months, not participating in regular resistance exercise, and having an average daily accelerometer step count less than the 50th percentile for age and gender).
Comparative Effectiveness Trial (CET) Exclusion criteria:
- unwilling to give written informed consent
- conditions that prevent regular exercise
- conditions that the medical or principal investigator determine to warrant exclusion
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: FitBrothers smartphone active app
Participants will be expected to engage with the FitBrothers app on a daily basis.
Daily alerts and notifications will engage users in daily use of the app and provide up-to-date information on users' progress.
Participant responses will also be used to evaluate additional or on-going support of users' needs (e.g., increase/ decrease prompts based on user preferences, tailored messages around a set goal, etc.).
To protect privacy and to ensure that the participant is the person completing the app activities, KB will uniquely identify the user's smartphone based off the device's "hardware footprint".
The app will upload all app activity data to the KB secured web server database.
|
The FitBrothers smartphone active app is designed to assist African American men with adopting and maintaining PA.
The app will be developed with significant input from African American men and contain self-monitoring, goal setting, reward, and educational components.
The app will include additional elements including PA adoption strategies, competitions, incentives, health information, and greater compatibility with activity monitoring devices.
The intervention is based on the Social Cognitive and Self-Determination theories and is culturally tailored.
|
|
Active Comparator: Comparator app
Nike Training Club is a free app available on iOS and Android platforms.
The app is designed to increase fitness in users through a variety of mechanisms.
Similar to FitBrothers, men will be able to track and monitor their physical activity level, set goals, engage in competitions, and upload activity data from a wearable.
They will also be provided with preset workouts, receive guidance from an expert, and receive personalized plans that automatically adapt to user behavior.
Unlike the FitBrothers app, the Nike Training Club app was not developed with input from African American men, does not track health information (e.g.
blood pressure, blood glucose), does not have a theoretical basis, and does not have specific strategies for maintenance.
|
The app is designed to increase fitness in users through a variety of mechanisms.
Users are able to track and monitor their physical activity level, set goals, engage in competitions, and upload activity data from a wearable.
They will also be provided with preset workouts, receive guidance from an expert, and receive personalized plans that automatically adapt to user behavior.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Physical activity-Acti Graph at 9 Months
Time Frame: Baseline and 9 months
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Steps per day will be collected using the ActiGraph WGT3X+BT accelerometer.
The device is worn on the wrist for a 7-day period.
|
Baseline and 9 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from Baseline in Weight at 9 Months
Time Frame: Baseline and 9 months
|
Weight of each participant will be measured with a scale.
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Baseline and 9 months
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Change from Baseline in Blood Pressure at 9 months
Time Frame: Baseline and 9 months
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Systolic and diastolic blood pressure will be measured at rest, under highly-controlled conditions.
All blood pressure measurements will be obtained using a Colin STBP-780 automated blood pressure monitor.
The first value will be discarded and the average of the last 3 values will be used, per standard Pennington Biomedical Research Center (PBRC) procedures.
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Baseline and 9 months
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Change from Baseline in Quality of Life Assessment at 9 Months
Time Frame: Baseline and 9 months
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The SF-36 Short Form Health Survey (SF-36) questionnaire will assess quality of life in a number of physiological and mental health domains. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability. |
Baseline and 9 months
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Change from Baseline in Dietary Habits at 9 Months
Time Frame: Baseline and 9 months
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The National Cancer Institute's Automated Self-Administered 24-hour Recall will be used to estimate daily intake of selected nutrients and macronutrients, food group servings, and alcohol. The NCI's Automated Self-Administered 24-hour Recall (ASA24) will be used to estimate daily intake of nutrients and macronutrients, food group servings, and alcohol. This tool enables self-administered 24-hour dietary recalls and calculates Healthy Eating Index scores (minimum score=0, maximum score=100). Healthy Eating Index measures diet quality and assesses conformance to federal dietary guidance. Higher scores reflect better dietary habits. |
Baseline and 9 months
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Satisfaction Assessment
Time Frame: 9 months
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A questionnaire will be used to assess each participant's satisfaction with the FitBrothers app. The questionnaire will assess satisfaction, helpfulness, enjoyment, and relevance across all components of app. Mean scores of 3.5 or greater, rated on a scale of 1 (poor) to 5 (excellent), will be deemed acceptable. |
9 months
|
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System Usability Scale (SUS)
Time Frame: 9 months
|
The System Usability Scale (SUS) is a validated, 10-item measure provides a global view of subjective usability for technology.
The 10 questions have 5 response options from "strongly disagree" to "strongly agree".
SUS yields a single number representing a composite measure of the overall usability of the system being studied.
Note that scores for individual items are not meaningful on their own.
To calculate the SUS score the score contributions from each item are summed.
Each item's score contribution ranges from 0 to 4. For items 1,3,5,7,and 9 the score contribution is the scale position minus 1.
For items 2,4,6,8 and 10, the contribution is 5 minus the scale position.
The sum of these scores are multiplied by 2.5 to obtain the overall value of SU.SUS scores have a range of 0 to 100.
SUS scores > 68 are considered acceptable.
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9 months
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FitBrothers App Usage
Time Frame: 9 months
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FitBrothers app usage will be assessed via a number of app usage sessions.
Usage will be collected using Webtrends.
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9 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Robert Newton, PHD, Pennington Biomedical Research Center
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0340
- 4R42MD014947-02 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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