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Pragmatic Factorial Cluster Trial of Framing and Comparators for Audit and Feedback

Pragmatic Factorial Cluster Trial of Framing and Comparators for Audit and Feedback Aiming to Address High Risk Prescribing in Nursing Homes in Ontario

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02979964
Enrollment
285
Registered
2016-12-02
Start date
2016-12-06
Completion date
2018-07-31
Last updated
2018-10-05

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

Conditions

High-risk Prescribing in Nursing Homes

Brief summary

Health Quality Ontario (HQO) is the provincial advisor on quality in health care. HQO currently conducts audit and feedback as a key quality improvement strategy. For example, it offers physicians working in long-term care homes with access to practice reports detailing rates of high-risk prescribing in comparison with others in Ontario and suggested change ideas. Research shows that providing this kind of feedback can lead to improvements in care. However, the size of these improvements depends how the feedback is presented. For instance, prior research suggests that how the results are 'framed' and what sort of benchmark the recipient is compared to may each affect how the physician will respond. This factorial trial tests each of these aspects of feedback design in the context of practice reports that nursing home physicians have already signed up to receive quarterly.

Interventions

Sponsors

Health Quality Ontario
CollaboratorOTHER
Women's College Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* a physician licensed by the College of Physicians and Surgeons of Ontario (CPSO); * practice in at least one LTC facility in Ontario;. * have voluntarily signed up to receive an HQO practice report

Exclusion criteria

* n/a

Design outcomes

Primary

MeasureTime frameDescription
CNS-active medication prescribing6 monthsmonthly number of CNS-active medications per resident (antipsychotics, opioids, benzodiazepines or antidepressants (including TCAs and trazodone))

Secondary

MeasureTime frameDescription
Benzodiazepine (or z-drug) rates6 monthsmonthly proportion
Antipsychotic rates6 monthsmonthly proportion
Antipsychotic prescribing6 monthsdays supplied (continuous)
Mean Antipsychotic dose6 monthsDose equivalent of antipsychotic dispensed (continuous)
Benzodiazepine (or z-drug) prescribing6 monthsdays supplied (continuous)
3+ CNS-active medications6 monthsmonthly proportion supplied three or more meds from the following classes: antipsychotics, opioids, benzodiazepines, or antidepressants (including TCAs and trazodone).
Anti-depressant prescribing6 monthsdays supplied (continuous) - balance measure
Anti-acid prescribing6 monthsdays supplied (continuous) - tracer outcome
Statin prescribing6 monthsdays supplied (continuous) - tracer outcome
Mean Benzodiazepine dose6 monthsDose equivalent of benzodiazepine dispensed (continuous)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026