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Not yet recruiting NCT07631858

Perspectives About Online Information

No phase Interventional Prostate Cancer

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Post (video) about prostate cancer, Post (text post) about prostate cancer, Survey.
Who it may be relevant to
Registry conditions: Prostate Cancer. Basic parameters: from 40 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The purpose of this research study is to understand the perspectives of U.S. adults on online information about prostate cancer. Study participants will receive different online information about prostate cancer to view such as a video post or text post, and complete a one-time online survey that will take approximately 10 minutes.

Interventions

  • Other Post (video) about prostate cancer
    Participants will review a post about prostate cancer.
  • Other Post (text post) about prostate cancer
    Participants will review a post about prostate cancer.
  • Other Survey
    The survey will include questions about demographics and internet use. It may also provide participants with resources about online information.

Primary outcome measures

  • Trust in the post, as measured by a 4-point Likert scale [Time frame: Post-intervention (~5 minutes)]
Secondary outcome measures (2)
  • Short-form Positive and Negative Affect Schedule (PANAS) Positive Score [Time frame: Post-intervention (~5 minutes)]
  • Short-form Positive and Negative Affect Schedule (PANAS) Negative Score [Time frame: Post-intervention (~5 minutes)]

Eligibility criteria

Inclusion criteria

  • U.S. adult age 40+ who identifies as Black and/or Hispanic
  • Enrolled in Dynata online survey panel
  • Willing and able to participate in the research study.

Exclusion criteria

  • Individuals up to age 39
  • Individuals living outside the U.S.
  • Individuals who are not Black and/or Hispanic

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Single group
Masking
Single blind
Primary purpose
Other

Study locations

United States · 1 center
  • NYU Langone Health — New York

Identifiers

NCT: NCT07631858 · 25-01456 · 1R01CA278997

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗