TY - JOUR
T1 - Impact of the diagnostic label for a low-risk prostate lesion
T2 - Protocol for two online factorial randomised experiments
AU - Bullen, James
AU - Nickel, Brooke
AU - McCaffery, Kirsten
AU - Wilt, Timothy J.
AU - Smith, Jenna
AU - Boroumand, Farzaneh
AU - Parker, Lisa
AU - Millar, Jeremy
AU - Brodersen, John Brandt
AU - Dahm, Philipp
AU - Delahunt, Brett
AU - Varma, Murali
AU - Glasziou, Paul
AU - Warden, Andrew
AU - Diller, Lawrence
AU - Billington, Larry
AU - Van Rensburg, Christo
AU - Bell, Katy
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ.
PY - 2024/8/9
Y1 - 2024/8/9
N2 - Introduction Many types of prostate cancer present minimal risk to a man's lifespan or well-being, but existing terminology makes it difficult for men to distinguish these from high-risk prostate cancers. This study aims to explore whether using an alternative label for low-risk prostate cancer influences management choice and anxiety levels among Australian men and their partners. Methods and analysis We will run two separate studies for Australian men and Australian women with a male partner. Both studies are between-subjects factorial (3×2) randomised online hypothetical experiments. Following consent, eligible participants will be randomised 1:1:1 to three labels: 'low-risk prostate cancer, Gleason Group 1', 'low-risk prostate neoplasm' or 'low-risk prostate lesion'. Participants will then undergo a second randomisation step with 1:1 allocation to the provision of detailed information on the benefits and harms of different management choices versus the provision of less detailed information about management choices. The required sample sizes are 1290 men and 1410 women. The primary outcome is the participant choice of their preferred management strategy: no immediate treatment (prostate-specific antigen (PSA)-based monitoring or active surveillance using PSA, MRI, biopsy with delayed treatment for disease progression) versus immediate treatment (prostatectomy or radiation therapy). Secondary outcomes include preferred management choice (from the four options listed above), diagnosis anxiety, management choice anxiety and management choice at a later time point (for participants who initially choose a monitoring strategy). Ethics and dissemination Ethics approval has been received from The University of Sydney Human Research Ethics Committee (2023/572). The results of the study will be published in a peer-reviewed medical journal and a plain language summary of the findings will be shared on the Wiser Healthcare publications page http://www.wiserhealthcare.org.au/category/publications/ Trial registration numbers Australian New Zealand Clinical Trials Registry (ID 386701 and 386889).
AB - Introduction Many types of prostate cancer present minimal risk to a man's lifespan or well-being, but existing terminology makes it difficult for men to distinguish these from high-risk prostate cancers. This study aims to explore whether using an alternative label for low-risk prostate cancer influences management choice and anxiety levels among Australian men and their partners. Methods and analysis We will run two separate studies for Australian men and Australian women with a male partner. Both studies are between-subjects factorial (3×2) randomised online hypothetical experiments. Following consent, eligible participants will be randomised 1:1:1 to three labels: 'low-risk prostate cancer, Gleason Group 1', 'low-risk prostate neoplasm' or 'low-risk prostate lesion'. Participants will then undergo a second randomisation step with 1:1 allocation to the provision of detailed information on the benefits and harms of different management choices versus the provision of less detailed information about management choices. The required sample sizes are 1290 men and 1410 women. The primary outcome is the participant choice of their preferred management strategy: no immediate treatment (prostate-specific antigen (PSA)-based monitoring or active surveillance using PSA, MRI, biopsy with delayed treatment for disease progression) versus immediate treatment (prostatectomy or radiation therapy). Secondary outcomes include preferred management choice (from the four options listed above), diagnosis anxiety, management choice anxiety and management choice at a later time point (for participants who initially choose a monitoring strategy). Ethics and dissemination Ethics approval has been received from The University of Sydney Human Research Ethics Committee (2023/572). The results of the study will be published in a peer-reviewed medical journal and a plain language summary of the findings will be shared on the Wiser Healthcare publications page http://www.wiserhealthcare.org.au/category/publications/ Trial registration numbers Australian New Zealand Clinical Trials Registry (ID 386701 and 386889).
KW - Adverse events
KW - Clinical Decision-Making
KW - Clinical Trial
KW - Patient-Centered Care
KW - Prostatic Neoplasms
KW - Surgical pathology
UR - https://www.scopus.com/pages/publications/85201064337
UR - https://www.scopus.com/pages/publications/85201064337#tab=citedBy
U2 - 10.1136/bmjopen-2024-085947
DO - 10.1136/bmjopen-2024-085947
M3 - Article
C2 - 39122400
AN - SCOPUS:85201064337
SN - 2044-6055
VL - 14
JO - BMJ open
JF - BMJ open
IS - 8
M1 - e085947
ER -