PA4Health Physical Activity App Open Pilot Study for African American Women

Sponsor
City University of New York, School of Public Health (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05714280
Collaborator
National Institute on Minority Health and Health Disparities (NIMHD) (NIH)
15
1
2.9
5.1

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: PA4Health Open Pilot
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Developing a Tailored, Theoretically-Driven Smartphone Physical Activity Intervention for African American Women
Anticipated Study Start Date :
Feb 1, 2023
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
May 1, 2023

Outcome Measures

Primary Outcome Measures

  1. System usability scale (SUS)-- app satisfaction [12 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.

  2. Metada; collected through app system [12 weeks]

    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

  1. Accelerometer [Participants will wear this device for 7 consecutive days at baseline and at 12 weeks(end of the intervention)]

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

  2. Fitbit data [Participants will wear this device daily during the 12-week intervention]

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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 64 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion: Eligible participants must:
  1. be ages 18-64

  2. identify as AA and female

  3. own a smartphone

  4. be able to provide consent

  5. not regularly physically active (i.e. less than 90 mins. of MVPA per week), 6) medically cleared for PA,

  1. have a valid email address, and 9) no previous engagement in the study.
Exclusion: Individuals will be excluded if they report:
  1. physical limitations to PA engagement

  2. significant medical conditions (e.g., heart failure)

  3. planned surgery in the next 6 months,

  4. pregnant or plan to become pregnant in the next 6 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 City University of New York School of Public Health & Health Policy New York New York United States 10027

Sponsors and Collaborators

  • City University of New York, School of Public Health
  • National Institute on Minority Health and Health Disparities (NIMHD)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
City University of New York, School of Public Health
ClinicalTrials.gov Identifier:
NCT05714280
Other Study ID Numbers:
  • CityUNYSPH
  • K23MD014164
First Posted:
Feb 6, 2023
Last Update Posted:
Feb 6, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by City University of New York, School of Public Health

Study Results

No Results Posted as of Feb 6, 2023