Doctor-Patient Communication About Colorectal Cancer Screening
This study is currently recruiting participants.
Verified May 2013 by Memorial Sloan-Kettering Cancer Center
Sponsor:
Memorial Sloan-Kettering Cancer Center
Collaborators:
Albert Einstein College of Medicine of Yeshiva University
HHC, Gun HIll and Tremont
NYC RING, Director
Virginia Commonwealth University
Information provided by (Responsible Party):
Memorial Sloan-Kettering Cancer Center
ClinicalTrials.gov Identifier:
NCT01534923
First received: February 10, 2012
Last updated: May 13, 2013
Last verified: May 2013
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Colorectal Cancer Screening |
Behavioral: surveys |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Doctor-Patient Communication About Colorectal Cancer Screening |
Resource links provided by NLM:
Further study details as provided by Memorial Sloan-Kettering Cancer Center:
Primary Outcome Measures:
- describe doctor-patient communication about CRC screening [ Time Frame: 2 years ] [ Designated as safety issue: No ]screening adherence through chart review (whether or not each patient has completed CRC screening by chart review within nine months post baseline, per Dr. McKee's recommendation). Screening adherence will be assessed through chart review by the RSA. The chart review will be completed approximately nine months following the patient's consultation with the doctor that was audio recorded.
Secondary Outcome Measures:
- quality of doctor-patient communication about CRC screening and low-income patients' screening outcomes. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
- examine the association between the quality of doctor-patient communication about CRC screening and low-income patients' screening outcomes [ Time Frame: 2 years ] [ Designated as safety issue: No ]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.
| Estimated Enrollment: | 225 |
| Study Start Date: | February 2012 |
| Estimated Study Completion Date: | February 2014 |
| Estimated Primary Completion Date: | February 2014 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Pts having colorectal cancer screening
The target sample of this study will be approximately 200 primary care physician-patient consultations who discuss CRC screening during the course of a clinical visit. Physician and patient participants will come from primary care practices associated with the New York City Research and Improvement Networking Group (NYC RING).
|
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 non-adherent patients.
|
Eligibility| Ages Eligible for Study: | 50 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Study Population
Five health centers of the NYC RING will participate in this project. All are located in underserved urban communities within the Bronx.
Criteria
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.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01534923
Contacts
| Contact: Carma Bylund, PhD | 646-888-0210 | |
| Contact: Jamie Ostroff, PhD | 646-888-0041 |
Locations
| United States, New York | |
| Albert Einstein College of Medicine | Recruiting |
| Bronx, New York, United States | |
| Contact: David Lounsbury, PhD | |
| Principal Investigator: David Lounsbury, PhD | |
| Hhc, Gun Hill and Tremont | Not yet recruiting |
| Bronx, New York, United States | |
| Contact: Jean Burg, MD | |
| Principal Investigator: Jean Burg, MD | |
Sponsors and Collaborators
Memorial Sloan-Kettering Cancer Center
Albert Einstein College of Medicine of Yeshiva University
HHC, Gun HIll and Tremont
NYC RING, Director
Virginia Commonwealth University
Investigators
| Principal Investigator: | Carma Bylund, PhD | Memorial Sloan-Kettering Cancer Center |
More Information
Additional Information:
No publications provided
| Responsible Party: | Memorial Sloan-Kettering Cancer Center |
| ClinicalTrials.gov Identifier: | NCT01534923 History of Changes |
| Other Study ID Numbers: | 12-017 |
| Study First Received: | February 10, 2012 |
| Last Updated: | May 13, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Memorial Sloan-Kettering Cancer Center:
|
Doctor-Patient Communication questionnaire survey 12-017 |
Additional relevant MeSH terms:
|
Colorectal Neoplasms Intestinal Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Neoplasms by Site Neoplasms |
Digestive System Diseases Gastrointestinal Diseases Colonic Diseases Intestinal Diseases Rectal Diseases |
ClinicalTrials.gov processed this record on May 16, 2013