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Re-Purposing the Ordering of 'Routine' Laboratory Tests in Hospitalized Medical Patients (RePORT Study)

Re-Purposing the Ordering of 'Routine' Laboratory Tests in Hospitalized Medical Patients (RePORT Study)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06119464
Enrollment
251817
Registered
2023-11-07
Start date
2023-01-02
Completion date
2026-10-01
Last updated
2026-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Utilization, Health Care

Keywords

Overutilization of lab test, Multimodal intervention, Lab test overuse, Laboratory, Hospital

Brief summary

Laboratory test overuse occurs when tests are ordered repetitively, without due consideration of impact on clinical status. Repetitive inpatient lab testing often provides limited value for patient outcomes while increasing healthcare costs, patient discomfort, and unnecessary transfusions and prolonging hospitalizations. The research study aims to reduce laboratory test overuse in hospitals through implementation of a comprehensive, multi-disciplinary, and multi-faceted intervention bundle that includes audit and feedback reports, clinician education, clinical decision support tool, and patient infographics across 14 hospitals in Alberta.

Detailed description

Background: Laboratory and Pathology testing contributes to rising health care expenditure. A relatively large percentage (up to 42%) of laboratory testing can be considered wasteful. Redundant testing alone has been estimated to waste up to 5 billion dollars annually in the United States of America. Laboratory over-utilization leads to false positives that promotes further inappropriate testing and procedures, interruption of normal sleep pattern of inpatients, as well as iatrogenic anemia and pain. A Canadian study showed significant hemoglobin reductions as a result of phlebotomy. Studies support the safe reduction of repetitive laboratory testing without negative effects on adverse events, readmission rates, critical care utilization, or mortality. The aim of this research study is the following: 1. To implement a multimodal intervention bundle containing healthcare provider and patient engagement tools for hospitalized medical inpatients in 14 hospitals across the province of Alberta in Canada using a cluster randomized stepped-wedge design 2. To evaluate the impact of the intervention bundle on laboratory test utilization of six target laboratory tests (complete blood count, electrolytes, creatinine, urea, partial thromboplastin time, and international normalized ratio), costs, and patient safety outcomes. This intervention bundle will be implemented across all the adult hospital sites in Alberta starting January 2023 and evaluated until October 2024.

Interventions

OTHERMultimodal Intervention: Education

The multimodal intervention bundle consists of education, audit and feedback, patient engagement, and system changes.

OTHERMultimodal Intervention: Audit and Feedback

The multimodal intervention bundle consists of education, audit and feedback, patient engagement, and system changes.

OTHERMultimodal Intervention: Patient Engagement

The multimodal intervention bundle consists of education, audit and feedback, patient engagement, and system changes.

OTHERMultimodal Intervention: System Changes

The multimodal intervention bundle consists of education, audit and feedback, patient engagement, and system changes.

Sponsors

University of Calgary
Lead SponsorOTHER
Alberta Health services
CollaboratorOTHER
University of British Columbia
CollaboratorOTHER
Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Stepped-wedge cluster randomized trial, randomizing the sequence of entry into intervention at a cluster level.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* all participants (patients and healthcare providers) within enrolled adult hospitals in Alberta of medical and hospitalist units during study period

Exclusion criteria

* outside of the above-mentioned province * hospitals not enrolled * non-medical units (eg. ICU, surgical, pediatric, obstetrical units)

Design outcomes

Primary

MeasureTime frameDescription
Number of routine laboratory tests ordered per patient-day in the intervention versus control periods1 year 9 monthsNumber of the six target laboratory tests (complete blood count, electrolytes, creatinine, urea, international normalized ratio and partial thromboplastin time) ordered per patient-day

Secondary

MeasureTime frameDescription
Costs associated with routine and all common laboratory test ordered1 year 9 monthsCosts of test and associated costs with and without intervention
Proportion of hospital patient lab-free days1 year 9 monthsNumber of hospital patient-days not associated with laboratory blood draws
Proportion of critically abnormal test results1 year 9 monthsAs defined by lab standards, we will track the proportion of critically abnormal test results
Length of stay1 year 9 monthsPatient length of stay on the unit
Transfer to Intensive Care Unit1 year 9 monthsTransfer rate to Intensive Care Unit
In-patient and 30-day patient mortality over study period30 days post dischargeMortality rate in hospital and at 30-days post discharge
30-day post discharge readmission rate30 days post dischargeHospital re-admission within 30 days post discharge
Number of all common laboratory tests1 year 9 monthsNumber of all common laboratory tests (tests that contribute to \>80% of hospital laboratory test utilization during study period) per patient-day.

Countries

Canada

Contacts

PRINCIPAL_INVESTIGATORAnshula Ambasta

University of Calgary

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 28, 2026