Randomized Trial of Trust in Online Videos About Prostate Cancer
1 other identifier
interventional
3,649
1 country
1
Brief Summary
The study team will evaluate the impact of video characteristics on health consumers' trust in online videos. Participants will be randomized to watch a video by one of four speakers about prostate cancer screening or clinical trials and complete a questionnaire (approximately 15 minutes total).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable prostate-cancer
Started Aug 2021
Shorter than P25 for not_applicable prostate-cancer
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 18, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 7, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
January 7, 2022
CompletedFirst Submitted
Initial submission to the registry
May 24, 2023
CompletedFirst Posted
Study publicly available on registry
June 2, 2023
CompletedApril 26, 2024
April 1, 2024
5 months
May 24, 2023
April 23, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Level of Trust in the Video
Trust will be reported as a score on a Likert scale and asked as the following question: How much do you trust the information in the video? The total range of score is 1-4, where (1) trust the information completely, (2) trust most of the information, (3) trust some of the information, (4) do not trust the information
Visit 1 (Day 1)
Study Arms (8)
Video About Screening with Black Doctor
EXPERIMENTALVideo About Screening with White Doctor
EXPERIMENTALVideo About Screening with Black Patient
EXPERIMENTALVideo About Screening with White Patient
EXPERIMENTALVideo about Clinical Trials with Black Doctor
EXPERIMENTALVideo about Clinical Trials with White Doctor
EXPERIMENTALVideo about Clinical Trials with Black Patient
EXPERIMENTALVideo about Clinical Trials with White Patient
EXPERIMENTALInterventions
Participants will view an online video with a Black doctor speaking about prostate cancer screening.
Participants will view an online video with a White doctor speaking about prostate cancer screening.
Participants will view an online video with a Black patient speaking about prostate cancer screening.
Participants will view an online video with a White patient speaking about prostate cancer screening.
Participants will view an online video with a Black doctor speaking about prostate cancer clinical trials.
Participants will view an online video with a White doctor speaking about prostate cancer clinical trials.
Participants will view an online video with a Black patient speaking about prostate cancer clinical trials.
Participants will view an online video with a White patient speaking about prostate cancer clinical trials.
Eligibility Criteria
You may qualify if:
- US adult age 40+
- Enrolled in Dynata online survey panel
You may not qualify if:
- Children
- Individuals living outside the U.S.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- NYU Langone Healthlead
- United States Department of Defensecollaborator
Study Sites (1)
NYU Langone Health
New York, New York, 10016, United States
Related Publications (1)
Loeb S, Ravenell JE, Gomez SL, Borno HT, Siu K, Sanchez Nolasco T, Byrne N, Wilson G, Griffith DM, Crocker R, Sherman R, Washington SL 3rd, Langford AT. The Effect of Racial Concordance on Patient Trust in Online Videos About Prostate Cancer: A Randomized Clinical Trial. JAMA Netw Open. 2023 Jul 3;6(7):e2324395. doi: 10.1001/jamanetworkopen.2023.24395.
PMID: 37466938RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Stacy Loeb, MD, MSc, PhD(hc)
NYU Langone Health
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 24, 2023
First Posted
June 2, 2023
Study Start
August 18, 2021
Primary Completion
January 7, 2022
Study Completion
January 7, 2022
Last Updated
April 26, 2024
Record last verified: 2024-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP
- Time Frame
- Beginning 9 months and ending 36 months following article publication or as required by a condition of awards and agreements supporting the research.
- Access Criteria
- The investigator who proposed to use the data after signing a data use agreement will have access to the data upon reasonable request for biomedical research purposes. Requests should be directed to stacy.loeb@nyulangone.org. To gain access, data requestors will need to sign a data access agreement.
Individual participant data needed for the proposed biomedical research use according to data use agreement from both parties will be shared.