CholGate - The Effect of Alerting Versus on Demand Computer Based Decision Support on Treatment of Dyslipidaemia by General Practitioners
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Purpose
Indirect evidence show alerting physicians with clinical decision support systems (CDSS) seem to change behaviour more than requiring users to actively initiate the system. However, randomized trials comparing these methods in a clinical setting are lacking. In this study we compare the effect of Alerting physicians with a CDSS or actively requiring initiation of CDSS on the adherence of Dutch general practitioners to the Cholesterol guideline of the Dutch college of General Practitioners.
| Condition | Intervention |
|---|---|
|
Decision Support Systems, Clinical |
Device: CholGate |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Open Label |
| Official Title: | The Effect of Alerting Versus on Demand Computer Based Decision Support on Treatment of Dyslipidaemia by General Practitioners - The CholGate Randomized Trial |
- The percentage of correctly screened patients using anonymous patient record data.
- The percentage of correctly treated patients using anonymous patient record data.
| Study Start Date: | June 2004 |
| Estimated Study Completion Date: | November 2005 |
Indirect evidence show alerting physicians with clinical decision support systems (CDSS) seem to change behaviour more than requiring users to actively initiate the system. However, randomized trials comparing these methods in a clinical setting are lacking. In this study we compare the effect of Alerting physicians with a CDSS or actively requiring initiation of CDSS on the adherence of Dutch general practitioners to the Cholesterol guideline of the Dutch college of General Practitioners, using a clinical decsion support system called CholGate. This system has the functionality to provide both Alerting and On-Demand decision support. Users are free to negate the advise provided by the decision support system. The trial will have a cluster randomized structure.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
Inclusion Criteria:
- All general practices using only Elias electronic patient records (ISOFT b.V)
- All patients meeting the screening and treatment criteria of the Dutch college of general practitioners cholesterol guideline
Exclusion Criteria:
- Practices that used paper based records
Contacts and Locations| Netherlands | |
| Department of Medical informatics, ErasmusMC | |
| Rotterdam, South Holland, Netherlands, 3000DR | |
| Principal Investigator: | Jacobus T van Wyk, MD, PhD | ErasmusMC University Medical Centre Rotterdam |
More Information
Additional Information:
Publications:
| ClinicalTrials.gov Identifier: | NCT00348751 History of Changes |
| Other Study ID Numbers: | 2000B161 |
| Study First Received: | June 29, 2006 |
| Last Updated: | May 7, 2008 |
| Health Authority: | Netherlands: The Central Committee on Research Involving Human Subjects (CCMO) |
Additional relevant MeSH terms:
|
Dyslipidemias Lipid Metabolism Disorders Metabolic Diseases |
ClinicalTrials.gov processed this record on May 22, 2013