Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01803750
Other study ID # 13-031
Secondary ID
Status Terminated
Phase N/A
First received February 28, 2013
Last updated February 19, 2015
Start date February 2013
Est. completion date February 2015

Study information

Verified date February 2015
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to understand primary care provider's knowledge, attitudes, and barriers to promoting evidence-based cancer screening and prevention practices for physicians with large Latino patient populations. The investigators will ask providers information on cancer screening and prevention practices by conducting one-on-one interviews. In addition, they would like to develop a committee of community providers to help design and implement cancer screening and prevention programs specifically for Latino patients based on the interview findings.


Recruitment information / eligibility

Status Terminated
Enrollment 3
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- New York State registered family practitioners and internal medicine physicians

- Minimum one half of their patients are Latino (provider self-reported)

- Currently practice in a small clinical setting (defined by no more than 5 providers) including community clinics, and/or private practice in Queens, Brooklyn, Bron and Staten Island, New York

- No active affiliation with a major hospital or academic institution.

Exclusion Criteria:

- Practicing medicine for less than 2 years

- Practicing in a setting where no health insurance is accepted

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • For New York State Registered Family Practitioners and Internal Medicine Physicians

Intervention

Behavioral:
in-depth, semi-structured interviews
In-depth interviews will be conducted by the Principle Investigator and will use a combination of open-ended and closed, fixed response questions. Interviews will be audio recorded if the participant agrees, and answers to fixed response questions will be marked for complete analysis. The data collection portion of the study is estimated to take approximately 8 months. Areas to be addressed in the open-ended portion of the interview include: 1) Knowledge, attitudes and beliefs toward evidence-based cancer screening and prevention approaches 2) Barriers to implementing evidence-based cancer screening practices in the individual provider's clinical setting 3) Preferences for mechanisms of information dissemination and implementation and 4) Ideas and methods to facilitate evidence-based practices to improve cancer screening in the Latino population. A community-based participatory committee (CBPC) will be formed with 5-7 key informants identified during the interview process.

Locations

Country Name City State
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (2)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary assess attitudes and barriers of community-based primary care providers serving large Latino patient populations toward implementing evidence-based practices for cancer screening and prevention. 1 year No
Secondary build the beginning of a Community-Based Participatory Committee and determine the feasibility of a network of community primary care providers serving large Latino patient populations with the purpose of disseminating, implementing and evaluating evidence-based practice for cancer screening and prevention. 1 year No