IMPlementation of gUideLines for the Management of Arterial hypertenSION. The IMPULSION Study
The objective of this protocol is to improve awareness, treatment, and control of arterial hypertension, within primary prevention of target organ damage, by implementing guidelines, after training of the participating physicians.
|Study Design:||Observational Model: Cohort
Time Perspective: Prospective
|Official Title:||IMPlementation of gUideLines for the Management of Arterial hypertenSION. The IMPULSION Study|
- Efficacy in arterial hypertension control [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Efficacy in reducing estimated risk of coronary heart disease [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Cost effectiveness of arterial hypertension control [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Differences between primary and secondary health care settings as well as teaching hospitals [ Time Frame: 6 months ] [ Designated as safety issue: No ]
|Study Start Date:||November 2006|
|Study Completion Date:||November 2007|
|Primary Completion Date:||November 2007 (Final data collection date for primary outcome measure)|
Physicians from 20 hospitals and 40 health centres (primary health care settings) were trained to implement guidelines in treating arterial hypertension.
There will be a baseline recording of patients with arterial hypertension and then physicians will have to complete a one page form (by ticking pre-specified boxes) about the baseline status of the patients and will have to report the measures they took to improve awareness, treatment, and effective control of arterial hypertension. After a six month effort, physicians will have to complete the same form at study completion. Previous training of physicians and the fact that they will have to report their success in treating hypertension will hopefully contribute to an increase in number of hypertensive patients at blood pressure target, and will minimise the target organ damage. The estimated reduction in coronary heart disease risk will be evaluated by a comparison of this risk (as evaluated by a risk engine, i.e. PROCAM) at study completion with that of baseline.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00416611
|Hellenic Atherosclerosis Society|
|Thessaloniki, Greece, 55132|
|Study Director:||Athyros G Athyros, MD||Clinical Trials Chair of Hellenic Atherosclerosis Society|