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NCT01241656 · ClinicalTrials.gov registry record · NA
Decision Support Interventions (DESI) for Prostate Cancer Screening - Study 1
A NA study of Healthy Men Age 50 Who Are Considering PSA Screening, sponsored by University of North Carolina, Chapel Hill.
- Completed
- Registry status
- NA
- Development phase
- 2,521
- Enrollment target
- 2
- Study locations
NCT01241656 is a NA study of Healthy Men Age 50 Who Are Considering PSA Screening that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 2,521 participants. The trial reports 2 study locations across 2 states.
The verdict
NCT01241656, a NA study of Healthy Men Age 50 Who Are Considering PSA Screening, has completed, sponsored by University of North Carolina, Chapel Hill.
- COMPLETED
- Registry status
- NA
- Development phase
- 2,521 participants
- Enrollment target
- 2
- Study locations
Study Summary
In this study we will compare 3 strategies for systematic delivery of prostate cancer screening decision support interventions (DESI) to usual care and examine their impact on screening decisions and subsequent healthcare utilization using a randomized control design. We hypothesize men who are given the opportunity to review a DESI by one of the 3 strategies will be less likely to opt for prostate cancer screening, and will have lower subsequent healthcare utilization than men in the control group.
Conditions Studied
Interventions
- BEHAVIORAL DESI for home viewing
- BEHAVIORAL DESI for viewing at Shared Medical Appointment
- BEHAVIORAL Option of SMA and DESI or DESI only
Study Locations (2)
California
- Palo Alto Medical Foundation Research Institute - Palo Alto
North Carolina
- University of North Carolina, Chapel Hill - Chapel Hill
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,521 participants |
| Start Date | 2011-01 |
| Est. Completion | 2012-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01241656
The ClinicalTrials.gov registry entry for NCT01241656 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 2,521 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Men Age 50 Who Are Considering PSA Screening appearing as the primary indexed condition, and to 3 interventions - of which DESI for home viewing is the first listed.
NCT01241656 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, North Carolina.
Frequently Asked Questions
What is clinical trial NCT01241656 about?
NCT01241656 is a clinical study titled "Decision Support Interventions (DESI) for Prostate Cancer Screening - Study 1". In this study we will compare 3 strategies for systematic delivery of prostate cancer screening decision support interventions (DESI) to usual care and examine their impact on screening decisions and subsequent healthcare utilization using a randomized control design. We hypothesize men who are giv...
What is the current status of trial NCT01241656?
This trial is currently completed. It is a NA study. The enrollment target is 2,521 participants. The study started on 2011-01. Estimated completion is 2012-12.
What conditions does trial NCT01241656 study?
This clinical trial studies the following conditions: Healthy Men Age 50 Who Are Considering PSA Screening.
What interventions are being tested in trial NCT01241656?
The interventions under investigation include: DESI for home viewing (BEHAVIORAL), DESI for viewing at Shared Medical Appointment (BEHAVIORAL), Option of SMA and DESI or DESI only (BEHAVIORAL).
Who is sponsoring clinical trial NCT01241656?
This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01241656 being conducted?
This trial has 2 study locations across California, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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