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Randomized Controlled Physical Activity App Intervention for Black Women

Developing a Tailored, Theoretically-Driven Smartphone Physical Activity Intervention for African American Women: RCT

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07114900
Acronym
PA4HealthRCT
Enrollment
50
Registered
2025-08-11
Start date
2025-03-09
Completion date
2026-06-30
Last updated
2025-09-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Activity

Keywords

Physical activity app, Wellness Text messaging, RCT

Brief summary

The goal of this study is test whether a physical activity app intervention compared to wellness text messaging intervention is more acceptable/engaging among Black women who want to increase their level of physical activity.

Detailed description

The goal of this K23 aim is to examine the acceptability and feasibility of the 8-week PA4Health intervention compared to a general wellness text program with 3 assessments (baseline, post-intervention \[8 weeks\] and 6 months). Participants will complete a single counseling session prior to starting the program. They complete an objective measure of physical activity by wearing an accelerometer for one week at each assessment time point. During the intervention, they will provided with a Fitbit wrist tracker, that will be synchronized to the app, to be worn during the 8-week intervention. Participants will be able to set goals for physical activity as well as monitor their progress toward achieving their goals. Following the trial, they will complete self-reports survey as well as objective measures of physical activity. They will also complete a single qualitative interview to assess their experience with the intervention and to provide feedback for modification.

Interventions

BEHAVIORALPA4Health app physical activity intervention

PA4Health app intervention Arm Description: During the app intervention consists of six components: 1) Goal setting and monitoring, 2) Tailored motivational messages based on survey data on barriers and facilitators of physical activity, 3) Education, which consists of twenty-two physical activity (PA) related topics, 4) a semi-structured chatroom where 3-5 participants per chatroom interact with one another to receive and provide peer support for PA, 5) Locator, which provides information about community resources (e.g., community parks, museums) based on participant's zip code, and 6) Steps, which allow participant to monitor their daily level of exercise. Participants wear a Fitbit tracker during the program

BEHAVIORALWellness Text Messaging Program

Participants set goal for PA and are encouraged to monitor their level of physical throughout the program. They receive a daily wellness related message during the program as a contact control. They also wear Fitbit tracker during the program.

Sponsors

Stony Brook University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

Eligible participants were: * ages 18-64, * Identify as AA and female * own a smartphone * be able to provide consent * not regularly physically active (i.e. less than 90 mins. of MVPA per week, * medically cleared for PA * have a valid email address, and 9) no previous engagement in the study.

Exclusion criteria

individuals were excluded if they report . physical limitations to PA engagement * significant medical conditions (e.g. heart failure) * planned surgery in the next 6 months * pregnant or plan to become pregnant in the next 6 months

Design outcomes

Primary

MeasureTime frameDescription
System Usability Scale (SUS)--app satisfactionEnd of 8 weeksDescription: The SUS measures ability of technology software. High levels of usability and acceptability of the app will be determined by a score greater than 70 on the SUS. Information will be used for improvement of the software. Time Frame: 8 weeks study
Metada data collected from app system8 weeksThis information will inform usage of patterns of participants, including how frequently the logged into the app system and the component of the app the more frequently or less frequently Time Frame: 8weeks

Secondary

MeasureTime frameDescription
Accelerometer/actigraph databaseline, 8 weeks, 6-month follow-upActigraph data will be analyzed to explore potential changes over time objectively collected min/week of MVPA
Physical activity constructsbaseline, 8 weeks, 6-month follow-upAssess changes in theoretical related constructs for physical activity, Stages of Change, Self-efficacy for Exercise, Physical Activity Enjoyment. Changes in mean scores from baseline to end intervention (8 weeks) will be assessed. Additionally changes in mean scores for these measures from end of intervention (8 weeks) and 6 month follow-up after controlling for baseline will be be explored.
Fitbit dataParticipants will wear this device daily during the active phase of the 8-week intervention and also until follow-up/ 6-month follow upFitbit data will be explored to estimate the effect of the intervention on mean steps/week over time

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026