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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02595775
Other study ID # 477-2014
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2015
Est. completion date September 2018

Study information

Verified date May 2017
Source Sunnybrook Health Sciences Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project aims to measure the impact of a physician report card (also called an audit & feedback report) on colonoscopy performance. Endoscopists in Ontario will be randomly assigned to either receive the endoscopist report card or to no feedback. Using Ontario health administrative data, the quality of colonoscopy will be compared between those who received the report card and those who do not. The investigators will also measure the effect of receiving endoscopist report card on colonoscopy performance amongst endoscopists who perform poorly at baseline compared to those who do not. Further, the acceptability of two educational interventions that aim to improve the quality of colonoscopy will be evaluated by conducting one-on-one interviews with select participants. This study is critical to ensure that Canadians have access to the highest quality colonoscopy possible.


Recruitment information / eligibility

Status Completed
Enrollment 833
Est. completion date September 2018
Est. primary completion date September 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All practising endoscopists in Ontario who performed at least 5 colonoscopies in 2014

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Individualized A/F report
Individualized A/F report containing 9 colonoscopy quality measures.
A/F report plus a high intensity intervention
E.g. Master class in colonoscopy
A/F report plus a low intensity intervention
E.g. Access to a video/presentation on good colonoscopy technique followed by a post presentation assessment.
A/F report alone


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Sunnybrook Health Sciences Centre Cancer Care Ontario

Outcome

Type Measure Description Time frame Safety issue
Primary Change in polypectomy rate from baseline Measure change in polypectomy rate from baseline At month 12
Secondary Additional outcome 1- Change in cecal intubation rate Change in cecal intubation rate from baseline At month 12
Secondary Additional outcome 2 - Change in annual colonoscopy volume Change in annual colonoscopy volume from baseline At month 12
Secondary Additional outcome 3 - Change in poor bowel preparation rate Change in poor bowel preparation rate from baseline At month 12
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