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Decision Support Study - A study on the impact of an evidence-based bedside electronic decision support tool on change in clinical performance in the care of Alberta hemodialysis patients

A study on the impact of an evidence-based bedside electronic decision support tool on change in clinical performance in the care of Alberta hemodialysis patients

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000489099
Enrollment
650
Registered
2005-07-12
Start date
2006-04-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

To determine the impact of a bedside decision support tool on the quality of care delivered to Alberta hemodialysis (HD) patients. The tool will recommend patient-specific evidence-based management changes to the nephrologist most responsible for each patient. This health services research concerns two of four Health Research Priority Themes: information management for health improvement and continuum of care and delivery models. Findings will be relevant to health professionals and decision-makers responsible for care of HD patients.

Interventions

A bedside decision support tool that provides patient specific, evidence-based management recommendations to rounding nephrologists responsible for each patient's medical management. The decision support tool will consist of an electronic database containing clinical information on study subjects. A series of simple algorithms will incorporate these clinical data and the tool will generate patient-specific recommendations for clinical management every two weeks. The recommendations will be pri

A bedside decision support tool that provides patient specific, evidence-based management recommendations to rounding nephrologists responsible for each patient's medical management. The decision support tool will consist of an electronic database containing clinical information on study subjects. A series of simple algorithms will incorporate these clinical data and the tool will generate patient-specific recommendations for clinical management every two weeks. The recommendations will be printed out on individual sheets of paper for each subject in the active treatment group and put on the clinical chart. The attending nephrologists will view the recommendations when they make their rounds. Clinical data will also be concurrently collected and stored for subjects in a control group, however no recommendations will be generated throughout the study. Study timeline - The electronic database will store data on both study groups an intial 6 month period but no recommendations will be generated, although rounding nephrologists will have access to the clinical data. For the following 18 months the electronically stored data will continue to be available to rounding nephrologists in both study groups, however, recommendations will be generated every two weeks for nephrologists treating the active group only.

Sponsors

Alberta Heritage Foundation for Medical Research
Lead SponsorCharities/Societies/Foundations

Study design

Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Patients receiving in-center hemodialysis in Alberta

Exclusion criteria

None

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026