Recruiting

mHealth App

Sponsor:

University of Oklahoma

Code:

NCT06651359

Conditions

Prostate Cancer

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Surveys for Quality of Life

Surveys and mHealth App access

Study Details

Brief 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.

Conditions

Prostate Cancer

Study ID

NCT06651359

Start date

Aug 24, 2025

Status verified date

Mar, 2026

Completion date

Nov, 2030

Anticipated

Primary completion date

Oct, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

\- Ethnically-diverse Black prostate cancer (CaP) survivors who are either native-born, Caribbean-born, or African-born

Exclusion Criteria:

  • Men from other races.
  • Men who have never been diagnosed with CaP
  • Men who have the inability to speak English

Study Design

Enrollment

248 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Supportive Care

Interventions and Outcome Measures

Arms

other: Control group

Participants in this arm will be eligible Black men who have prostate cancer and are either currently undergoing treatment or are cancer survivors.

experimental: Intervention group

Participants in this arm will be eligible Black men who have prostate cancer and are either currently undergoing treatment or are cancer survivors, who are given access to the mHealth app for this study.

Interventions

Surveys 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).

Surveys 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.

Primary outcome measure

  • Overall Quality of Life (QoL) assessment in Black men with prostate cancer [ Time Frame: 12 months ]

Central Contacts and Locations

Central contacts

Locations

Florida State University

Recruiting

Tallahassee, Florida, United States, 32306-4310

Georgia College & State University

Recruiting

Milledgeville, Georgia, United States, 31061

University of Oklahoma HSC

Recruiting

Oklahoma City, Oklahoma, United States, 73104

Contacts

Motolani Adedipe, PhD, DPh, MS

Motolani-adedipe@ouhsc.edu

Principal Investigator:

Motolani Adedipe

More Information

Sponsor

University of Oklahoma

Last update posted

Apr 1, 2026

Last verified

Mar, 2026

Keywords

  • mHealth
  • Black men
  • Black survivors
  • native-born Black man
  • African-born Black man
  • Caribbeanborn Black man

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Oklahoma on 2026-04-01.