- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03304860
Child-Physician Recommendation on Parental Adherence to Colorectal Cancer Screening
November 6, 2018 updated by: NYU Langone Health
Physician recommendation has been shown to be one of the most significant predictors for colorectal cancer (CRC) screening.
This study aims to identify the amount of parents of internal medicine residents at NYU who are eligible for CRC screening but have not received it.
Investigators will perform an intervention and quantify the amount of parents eligible for CRC screening after the intervention.
This study will entail sending 2 brief surveys (one before the intervention and one after) which determine if the parents of the residents are eligible for CRC screening.
The intervention will be asking the residents with eligible parents to have a discussion with their parents about CRC screening options and to address their concerns.
Investigators will provide a one page document the residents can give their parents as a reference as part of the intervention.
Study Overview
Study Type
Interventional
Enrollment (Actual)
59
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
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New York, New York, United States, 10016
- New York University School of Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Internal medicine residents at NYU - PGY1, PGY2, and PGY3 during 2017-2018 academic year
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: CRC screening Survey
Residents with parents eligible for CRC screening will be asked to provide their e-mail address, solely for the use of distributing the follow up survey so it can be linked to 2 brief (3-5 min) surveys
|
Survey with 4-7 questions about each parents' demographics and CRC screening history.
Depending on answers, provided a CRC screening document and asked to discuss screening with parents, followed by a brief survey in 4 months
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in CRC screening rate of eligible parents of internal medicine residents at NYU from before to after the intervention
Time Frame: Baseline to 6 Months
|
Baseline to 6 Months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Mark Pochapin, MD, NYU Langone Health
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2017
Primary Completion (Actual)
July 1, 2018
Study Completion (Actual)
July 1, 2018
Study Registration Dates
First Submitted
October 4, 2017
First Submitted That Met QC Criteria
October 4, 2017
First Posted (Actual)
October 9, 2017
Study Record Updates
Last Update Posted (Actual)
November 7, 2018
Last Update Submitted That Met QC Criteria
November 6, 2018
Last Verified
November 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17-00570
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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