The BALANCE Study: BlAck and Mixed Men's Lived Experience With Prostate cANCEr-Diversity in Prostate Cancer PROMS Study

Starting soon

Conditions studied: Prostate Cancer

In brief

The BALANCE study is a prospective Patient Reported Outcomes Measures (PROMs) study developed to look at the quality of life (QoL) of patients diagnosed with prostate cancer (PCa) in communities underrepresented in research, especially Black men of African, and Caribbean ancestry as well as men of Mixed ethnicity. This study will also investigate various PCa treatment types and their mental health impact on patients. There is a lack of research on PROMs in diverse populations. Collecting PROMs specifically from Black men and individuals with prostates who are receiving/have received treatment for PCa is essential for understanding their unique post-treatment experiences. The insights are vital to addressing documented disparities, tailoring supportive care and ultimately providing equitable health outcomes. Participants in this study will be asked to complete a questionnaire (either electronically or hardcopy) to share their insights following their PCa diagnosis.

Key facts

Study ID

NCT07529418

Run by

Institute of Cancer Research, United Kingdom

People needed

800

Starts

2026-05-05

Expected to finish

2027-03-01

Last updated by the study team

2026-04-14

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• In order to be eligible to participate in this study, a subject must meet all of the following criteria:
• Age ≥ 18 years;
• Be of either:
• Black African ancestry; OR
• Black African-Caribbean ancestry; OR
• Mixed Black ancestry.
• Diagnosed with PCa;
• Assigned male at birth;
• Participants with access to digital devices (smartphones, tablets, computers) or able to complete hardcopy versions of the survey;
• Participants willing to participate and provide informed consent.

You may not qualify if…

• A potential subject who meets any of the following criteria will be excluded from participation in this study:
• Participants having no diagnosis of PCa;
• Participants unable to provide consent;
• Participants assigned female at birth.

Full record on ClinicalTrials.gov

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