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NCT02414191 Clinical Trial

Feedback on Perioperative Temperature Management and Patient Outcomes: Three-arm Trial to Compare Feedback

Hypothermia Clinical Trial

Official title:
Effect of Audit and Feedback on Physicians' Perioperative Temperature Management and Patient Outcomes: A Three-arm Cluster Randomized Controlled Trial to Compare Benchmarked and Ranked Feedback

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02414191
Other study ID # 20140117-01H
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2015
Est. completion date April 6, 2018

Study information
Verified date March 2020
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators aim to assess the impact of benchmarked and ranked feedback on anesthesiologists' perioperative temperature management and subsequent patient outcomes.

Recruitment information / eligibility
Status Completed
Enrollment 45
Est. completion date April 6, 2018
Est. primary completion date April 6, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Staff Anesthesiologists at The Ottawa Hospital

Exclusion Criteria:

- none

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Benchmarked Feedback
Participants receive data, during the 6 month intervention phase, regarding their monthly temperature management performance in the form of benchmarked feedback, which is the measure of their performance in comparison the standard set by the hospital.
• Ranked Feedback
Participants receive data, during the 6 month intervention phase, regarding their monthly temperature management performance in the form of ranked feedback, which is the measure of their performance in comparison to their peers.

Locations
Country Name City State
Canada The Ottawa Hospital Ottawa Ontario

Sponsors (1)
Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Patient peri-operative temperature Within the 30 minutes immediately before or the 15 minutes immediately after anesthesia end time.
Secondary Intraoperative warming device usage perioperative intraoperative
Secondary Patient post-operative surgical site infection (SSI) rate Within 30 days of surgery
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