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NCT01534923 Clinical Trial

Doctor-Patient Communication About Colorectal Cancer Screening

Colorectal Cancer Screening Clinical Trial

Official title:
Doctor-Patient Communication About Colorectal Cancer Screening

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01534923
Other study ID # 12-017
Secondary ID
Status Completed
Phase
First received
Last updated
Start date February 7, 2012
Est. completion date December 26, 2019

Study information
Verified date December 2019
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to learn more about doctor-patient communication about colon cancer screening. This study will also look to see if there are differences in those who get colon cancer screening based on the discussion the doctor had with the patient.

Recruitment information / eligibility
Status Completed
Enrollment 76
Est. completion date December 26, 2019
Est. primary completion date December 26, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years to 75 Years
Eligibility Inclusion Criteria:

Physicians

- Attending physicians or third year residents specializing in internal medicine or family medicine, as per the medical director from the clinic.

- Clinic is based at a NYC RING-affiliated practice.

- English speaking; Due to limited resources, we cannot have each audio recorded consultation translated therefore, the consultation needs to be in English.

Patients

- Ages 50-75 years old, per the United States Preventive Services Task Force recommendations for screening. This will be determined by a pre-screening of medical records by the RSA.

- Due for colorectal cancer screening at the time of the visit, ascertained through patient self-report (e.g., no colonoscopy within the past 10 years, no flexible sigmoidoscopy or barium enema within the past five years, and no FOBT within the past year).

- Coming for either an annual physical exam or chronic care follow up visit, per patient self-report.

- Planning to consult with the physician in English, per patient self-report. Due to limited resources, we cannot have each audio recorded consultation translated therefore, the consultation needs to be in English.

Exclusion Criteria:

- History of colorectal cancer, per patient self-report or per EMR..

- History of polyps being removed, per patient self-report.

- Colonoscopy scheduled in EMR at time of screening.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• surveys
The intervention will be the audio-recording of the physician-patient consultation, patient and doctor surveys. These audio recordings will be coded. It will also include follow-up phone calls with patients.

Locations
Country Name City State
United States Albert Einstein College of Medicine Bronx New York
United States Hhc, Gun Hill and Tremont Bronx New York

Sponsors (5)
Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center Albert Einstein College of Medicine, HHC, Gun HIll and Tremont, NYC RING, Director, Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary describe doctor-patient communication about CRC screening screening adherence through self report. Screening adherence will be assessed by contacting the patients and asking them if they received the CRC screening test their doctor ordered at the audio recorded visit. 2 years
Secondary quality of doctor-patient communication about CRC screening and low-income patients' screening outcomes. 2 years
Secondary examine the association between the quality of doctor-patient communication about CRC screening and low-income patients' screening outcomes intent to be screened (immediately after the consultation) using the item from Geller et al.25 and 2) self-efficacy for screening (immediately after consultation) in case there are few events of actual screening. 2 years
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