Exercise Clinical Trial
Official title:
Smartphone App to Increase and Maintain Physical Activity in African American Men (FitBrothers) Phase II
Low physical activity levels contribute to African American men experiencing health disparities across a number of chronic diseases. Studies have been effective in increasing physical activity levels in African American men; but few have targeted maintenance of behavior change and none have utilized emerging technologies. The purpose of the current study is to further develop a mobile phone application for African American men that will help them initiate and maintain their physical activity levels.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | January 1, 2025 |
Est. primary completion date | September 1, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 30 Years and older |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | Pennington Biomedical Research Center | Baton Rouge | Louisiana |
United States | Klein Buendel, Inc. | Golden | Colorado |
United States | Georgetown University | Washington | District of Columbia |
Lead Sponsor | Collaborator |
---|---|
Klein Buendel, Inc. | Georgetown University, National Institute on Minority Health and Health Disparities (NIMHD), Pennington Biomedical Research Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from Baseline in Physical activity-Acti Graph at 9 Months | 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 | Change from Baseline in Weight at 9 Months | Weight of each participant will be measured with a scale. | Baseline and 9 months | |
Secondary | Change from Baseline in Blood Pressure at 9 months | 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. | Baseline and 9 months | |
Secondary | Change from Baseline in Quality of Life Assessment at 9 Months | 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 | |
Secondary | Change from Baseline in Dietary Habits at 9 Months | 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 | |
Secondary | Satisfaction Assessment | 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 | |
Secondary | System Usability Scale (SUS) | 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. | 9 months | |
Secondary | FitBrothers App Usage | FitBrothers app usage will be assessed via a number of app usage sessions. Usage will be collected using Webtrends. | 9 months |
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