RecruitingNot ApplicableNCT06651359

Using a mHealth App to Improve Quality-of-Life Outcomes in Black Prostate Cancer Survivors

Development and Preliminary Evaluation of a Tailored mHealth App Designed to Improve Quality-of-Life Outcomes in Ethnically-Diverse Black Prostate Cancer Survivors (SAFE-CaPs)


Sponsor

University of Oklahoma

Enrollment

248 participants

Start Date

Aug 24, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to ensure that the mobile health application for Black patients with prostate cancer (either actively undergoing treatment or survivors) is usable and acceptable to patients, get feedback about how to improve the app and assess its usefulness in examining their quality of life.


Eligibility

Sex: MALEMin Age: 18 Years

Inclusion Criteria1

  • \- Ethnically-diverse Black prostate cancer (CaP) survivors who are either native-born, Caribbean-born, or African-born, within the early phase of their CaP survivorship journey (defined as within the first five years after diagnosis).

Exclusion Criteria5

  • Men from other races.
  • Men who have never been diagnosed with CaP
  • Men who have the inability to speak English
  • Men who do not own a smartphone
  • Black CaP survivors who are over 5 years since the time of diagnosis

Interventions

BEHAVIORALSurveys for Quality of Life

This group will take scheduled electronic surveys (at the beginning of the study, months 3, 6, 9, and 12) to assess the overall impact of prostate cancer on quality of life (QoL).

BEHAVIORALSurveys and mHealth App access

This group will take scheduled electronic surveys (at the beginning of the study, months 3, 6, 9, and 12) to assess the overall impact of prostate cancer on quality of life (QoL). Additionally, they will have a brief "initial study visit," in-person or virtually, to review the app use. This arm of participants will use the mobile application at home for 12 months. During the first 12 weeks, the application will send daily surveys about symptoms, dietary and physical activities, weekly surveys about their mood, and an assessment of their overall QoL every 3 months. The app will provide tailored educational content, including short readings, videos, and audio recordings, to help users learn more about managing symptoms and improving their functioning. After 12 months of app use, an interview will be conducted to gather feedback about their experiences with the app. The information collected from these interviews will be analyzed to further enhance and improve the app's functionality.


Locations(3)

Florida State University

Tallahassee, Florida, United States

Georgia College & State University

Milledgeville, Georgia, United States

University of Oklahoma HSC

Oklahoma City, Oklahoma, United States

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NCT06651359


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