Reducing Lab Tests to Prevent Hospital Infections
(RePORT-BC Trial)
Trial Summary
Will I have to stop taking my current medications?
The trial information does not specify whether participants need to stop taking their current medications.
What data supports the effectiveness of the treatment Laboratory Test Overuse Intervention Bundle in reducing hospital infections?
Research shows that interventions aimed at reducing unnecessary lab tests in hospitals can lower the number of tests ordered without negatively affecting patient outcomes. For example, a study in long-term acute care hospitals found that tailored strategies to reduce lab test overuse led to fewer tests being ordered, which can help prevent potential harm and infections from unnecessary blood draws.12345
Is the Laboratory Test Overuse (LTO) Bundle safe for humans?
How is the LTO Bundle treatment different from other treatments for reducing lab test overuse?
The LTO Bundle is unique because it focuses on reducing unnecessary and repetitive laboratory tests in hospitals, which can help prevent infections and improve patient care. Unlike other treatments, it involves a systematic approach to change hospital staff behavior and awareness about lab test ordering, rather than relying on medication or direct patient interventions.12378
What is the purpose of this trial?
The goal of this stepped-wedge cluster randomized trial is to assess the impact of a laboratory test overuse intervention bundle on laboratory test utilization in 6 health authorities (16 hospitals) in British Columbia. The main question it aims to answer is if the intervention bundle, inclusive of healthcare provider and patient engagement tools, can be effectively implemented for hospitalized medical inpatients in 16 hospitals across BC and reduce laboratory test over-use. Researchers will compare hospital clusters that receive the intervention at different (sequential) time points to see if there are significant changes in the measured outcomes after the intervention.
Research Team
Anshula Ambasta
Principal Investigator
University of British Columbia
Eligibility Criteria
This trial is for adult patients admitted under general internal medicine or family medicine in selected hospitals, as well as healthcare providers involved in their care. It includes physicians and allied health staff who can order labs. The study spans from May 2024 to October 2026.Inclusion Criteria
Exclusion Criteria
Timeline
Control Period
Initial control period to collect baseline data before intervention
Pilot Phase
Feasibility assessment of intervention tools and adaptation to local context
Intervention Implementation
Sequential implementation of the intervention bundle in hospital clusters
Post-Implementation Follow-up
Evaluation of the impact of intervention tools without dedicated personnel support
Treatment Details
Interventions
- Laboratory test overuse (LTO) Bundle
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of British Columbia
Lead Sponsor
Island Health
Collaborator
Northern Hospital, Australia
Collaborator
Canadian Institutes of Health Research (CIHR)
Collaborator
Providence Health & Services
Collaborator
Vancouver Coastal Health
Collaborator
Fraser Health
Collaborator
Interior Health
Industry Sponsor