Decision Support Systems, Clinical Clinical Trial
— EBMeDSOfficial title:
Patient Specific Automatic Reminders in Primary Care - the EBMeDS Randomised Trial
Verified date | December 2012 |
Source | University of Tampere |
Contact | n/a |
Is FDA regulated | No |
Health authority | Finland: Ethics Committee |
Study type | Interventional |
The purpose of this study is to analyze the effect of the Evidence-Based Medicine electronic
Decision Support (EBMeDS) automatic reminders in primary health care.
Hypothesis (1)is that in the intervention group the total number of EBMeDS reminders will
decrease compared to the control group.
Hypothesis (2) is that in the intervention group the quality measures will increase faster
compared to the control group at follow-up time.
Status | Completed |
Enrollment | 12101 |
Est. completion date | February 2011 |
Est. primary completion date | February 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - All residents of Sipoo who have patient ID number in the Mediatri electronic patient record system in Sipoo Health Centre Exclusion Criteria: - Those residents who's occupational health care is produced by Sipoo Health Centre |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Health Services Research
Country | Name | City | State |
---|---|---|---|
Finland | University of Tampere; School of Health Sciences | Tampere |
Lead Sponsor | Collaborator |
---|---|
University of Tampere | Duodecim Medical Publications Ltd., National Institute for Health and Welfare, Finland, ProWellness Ltd., The Finnish Funding Agency for Technology and Innovation (TEKES), The Finnish Medical Society Duodecim |
Finland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The number of reminders triggered (in relation to the number of eligible patients, Ri/Ni) during repeated Virtual Health Checks (VHCs) | VHC will be performed once a week for the whole study population, beginning at baseline and before randomisation. The main outcome measure is Ri/Ni at follow-up time after commencement of the study where Ri is the total number of reminders triggered by the patient record data in intervention and in control group at the time of analysis, and Ni is the total number of patients. | Follow-up time max one and half year | Yes |
Secondary | Specific clinical measures compared to an intervention and a control group | Clinical measures as mean values of laboratory parameters, for example a mean level of HbA1c, a mean level of total cholesterol. | Yes |
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