ClinicalTrials.gg
CompletedNCT05886751Updated Apr 26, 2024

Randomized Trial of Trust in Online Videos About Prostate Cancer

An interventional study of Black Doctor Screening Video and White Doctor Screening Video in Prostate Cancer, sponsored by NYU Langone Health. Completed at 1 site in United States. Open to participants aged 40 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-04-26.

Sponsored by NYU Langone Health · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 9 months after the study started (first participant enrolled Aug 2021, registered May 2023).
Phase
Not applicable
Study type
Interventional
Enrollment
3,649
Allocation
Randomized
Ages
40 Years and older
Sex
All
01

Study 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).

02

Conditions studied

  • Prostate Cancer

Browse trials for

Keywords

  • Trust
03

In context

Prostatic Neoplasms

6,484 studies on the registry are indexed under Prostatic Neoplasms; 1,415 are open to participants now.

This study's enrollment of 3,649 is above the median of 58 across 4,908 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

NYU Langone Health is the lead sponsor of 1,421 studies on the registry; 254 are open to participants now.

Of its 231 completed or terminated interventional studies of FDA-regulated products, 195 (84%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. US adult age 40+
  2. Enrolled in Dynata online survey panel

Exclusion criteria

Exclusion Criteria:

  1. Children
  2. Individuals living outside the U.S.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
3,649 participants (actual)

Study arms

  • Experimental
    Video About Screening with Black Doctor

    Other: Black Doctor Screening Video

  • Experimental
    Video About Screening with White Doctor

    Other: White Doctor Screening Video

  • Experimental
    Video About Screening with Black Patient

    Other: Black Patient Screening Video

  • Experimental
    Video About Screening with White Patient

    Other: White Patient Screening Video

  • Experimental
    Video about Clinical Trials with Black Doctor

    Other: Black Doctor Clinical Trials Video

  • Experimental
    Video about Clinical Trials with White Doctor

    Other: White Doctor Clinical Trials Video

  • Experimental
    Video about Clinical Trials with Black Patient

    Other: Black Patient Clinical Trials Video

  • Experimental
    Video about Clinical Trials with White Patient

    Other: White Patient Clinical Trials Video

Interventions

  • OtherBlack Doctor Screening Video

    Participants will view an online video with a Black doctor speaking about prostate cancer screening.

  • OtherWhite Doctor Screening Video

    Participants will view an online video with a White doctor speaking about prostate cancer screening.

  • OtherBlack Patient Screening Video

    Participants will view an online video with a Black patient speaking about prostate cancer screening.

  • OtherWhite Patient Screening Video

    Participants will view an online video with a White patient speaking about prostate cancer screening.

  • OtherBlack Doctor Clinical Trials Video

    Participants will view an online video with a Black doctor speaking about prostate cancer clinical trials.

  • OtherWhite Doctor Clinical Trials Video

    Participants will view an online video with a White doctor speaking about prostate cancer clinical trials.

  • OtherBlack Patient Clinical Trials Video

    Participants will view an online video with a Black patient speaking about prostate cancer clinical trials.

  • OtherWhite Patient Clinical Trials Video

    Participants will view an online video with a White patient speaking about prostate cancer clinical trials.

06

What researchers measure

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

    Time frame: Visit 1 (Day 1)

07

Study locations

1 site
  • NYU Langone Health
    New York, New York 10016, United States
08

References and documents

Publications

  • 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. PubMed 37466938 ↗

Study documents

  • Informed consent form · May 12, 2022

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: Yes — Individual participant data needed for the proposed biomedical research use according to data use agreement from both parties will be shared.

Supporting information: Study protocol, Statistical analysis plan

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.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2021 to primary completion in Jan 2022, 4 months.

Of 1,018 non-industry interventional studies with no phase under Prostatic Neoplasms, half reached primary completion within 45 months of starting (the median), counting those still running; a quarter within 23 and three quarters within 87. This study's 4 months is below that.

Counting every sponsor, half of 1,063 studies reached it within 45 months; a quarter within 22 and three quarters within 87.

How these figures are worked out, and which studies are left out of them.

Registered
May 24, 2023
First posted
Jun 2, 2023
StartActual
Aug 18, 2021
Primary completionActual
Jan 7, 2022
CompletionActual
Jan 7, 2022
Last update
Apr 26, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 26, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05886751
Lead sponsor
NYU Langone Health
Collaborators
United States Department of Defense
Responsible party
Sponsor
First posted
Jun 2, 2023
Start date
Aug 18, 2021
Primary completion
Jan 7, 2022
Completion
Jan 7, 2022
Last update
Apr 26, 2024

Study contacts

Stacy Loeb, MD, MSc, PhD(hc)
principal investigator · NYU Langone Health

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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