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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06361056
Other study ID # LCCC2140
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date May 2, 2022
Est. completion date January 2026

Study information

Verified date April 2024
Source UNC Lineberger Comprehensive Cancer Center
Contact Lauren Matthews
Phone 919-843-5321
Email lauren_matthews@med.unc.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study explores the overall feasibility, impact, and satisfaction of using the "mHealth app" on clinic workflow for Black or African American women diagnosed with breast cancer. The "mHealth app" which can be used as a platform to share clinical trial education and communication, was created and tested in previous steps of this study.


Description:

A patient advisory council (PAC) was recruited from established hospital and community networks (North Carolina Cancer Hospital's Patient and Family Advisory Board, and the Lineberger Community Outreach and Engagement Office's Community Advisory Board). The PAC informed the content of interview guides, questionnaire/survey instruments, and mHealth app design, and will be involved in the analyses of qualitative and quantitative data, and dissemination of study results. After analysis of the in-depth interviews, the Connected Health for Applications and Interventions (CHAI) core staff developed a progressive web application "mHealth app". mHealth app was tested in a pilot study included 20 African American (AA) patients diagnosed with breast cancer were interviewed to answer questions that will better inform the clinical trial education and communication needs of Black women with breast cancer. Eighty African American women with newly diagnosed breast cancer who have access to a mobile device or computer will be recruited for the study intervention. Women will receive access to the "mHealth" app, a list of available clinical trials within a 50-mile radius of their zip code, and the existing standard of care packet of cancer center resources. Participants will complete a brief questionnaire that will assess clinical trial knowledge, how often a clinical trial discussion occurred during their oncology appointment, and if a therapeutic trial was offered.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date January 2026
Est. primary completion date January 2025
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - 18 years or older - English speaking - Able and willing to participate to complete the survey. - Have access to a mobile device or computer. - Diagnosed with breast cancer. - Identify as African American Exclusion Criteria: - Inability to read and speak English. - Dementia altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Survey
All participants will complete a brief questionnaire.
mHealth app
Eighty Black women with newly diagnosed breast cancer (inclusive of all stages) and who have access to a mobile device or computer will be recruited to the study intervention.

Locations

Country Name City State
United States UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina

Sponsors (1)

Lead Sponsor Collaborator
UNC Lineberger Comprehensive Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility of Mobile Health Application (mHealth app)- subjects The feasibility of the mHealth app will be determined by the percentage of subjects who enrolled and completed trial requirements. Up to 1 year
Primary Feasibility of Mobile Health Application (mHealth app) - Clinicians and staff Clinicians and staff will be interviewed to assess feasibility. Up to 1 year
Secondary Overall satisfaction Overall satisfaction will be assessed by survey questions administered to study participants. The rate of participants' satisfactions will be reported. Up to 1 year
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