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PA4Health Physical Activity App Open Pilot Study for African American Women

Not Applicable
Completed
Conditions
Test Acceptability/Usability of a Physical Activity App Developed for African American Women
Registration Number
NCT05714280
Lead Sponsor
City University of New York, School of Public Health
Brief Summary

Test the acceptability of a smartphone physical activity app for African American women

Detailed Description

The goal of this aim is to collect data that guide the refinement of intervention components and structure to increase appeal to AA women. Fifteen physically inactive AA women will participate in a 12-week study examining the feasibility, acceptability, and usage of the PA4Health app. They will receive a Fitbit tracker to be worn during the trial. Following the trial, participants will complete self-report measures as well as a semi-structured interview to learn about their experience in using the app, any experienced difficulties, and recommendations for improving the acceptance and usage of the app.

Intervention components: The intervention components include: tailored daily text intervention text message, educational feature, goal setting and monitoring, and an activity locator that allow participants to enter their zip code and view available resources for physical activity.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
15
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
System usability scale (SUS)-- app satisfaction8 weeks study

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.

Metada; collected through app system8weeks

This 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

Secondary Outcome Measures
NameTimeMethod
AccelerometerParticipants will wear this device for 7 consecutive days at baseline and at 8 weeks(end of the intervention)

actigraph data will be analyzed to explore potential changes over time objectively collected min/week of MVPA

Fitbit dataParticipants will wear this device daily during the 8-week intervention

Fitbit data will be explored to estimate the effect of the intervention on mean steps/week over time

Trial Locations

Locations (1)

City University of New York School of Public Health & Health Policy

🇺🇸

New York, New York, United States

City University of New York School of Public Health & Health Policy
🇺🇸New York, New York, United States
Michele Kiely, Dr.P.H.
Contact
646-364-9775
Michele.Kiely@sph.cuny.edu
Marie A Sillice, Ph.D
Principal Investigator

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