Pharmacy Implementation Trial: Adherence to Antihypertensive Therapy
- Conditions
- Hypertension
- Interventions
- Other: extensive implementation programmeOther: control
- Registration Number
- NCT00460343
- Lead Sponsor
- Radboud University Medical Center
- Brief Summary
The purpose of this study is to determine the effectiveness of maximal support of community pharmacies to implement a pharmaceutical care model for establishing and - if necessary - improving adherence to antihypertensive medication in patients with medication-resistant hypertension.
- Detailed Description
Cardiovascular disease is the main cause of death in large parts of the world. Hypertension is an important risk factor for cardiovascular disease. Although hypertension treatment has improved in the last decade, the effectiveness of antihypertensive therapy still needs attention. Adherence to medication appears to play an important role in that.
Pharmacists can support the general practitioners in their efforts to optimize antihypertensive therapy, by establishing adherence to medication of patients with hypertension in spite of the use of one or more antihypertensive drugs. This is performed with the electronic Medication Event Monitoring System (MEMSĀ®). Registered adherence and accompanying blood pressure are discussed with the patient by the GP.
Implementation of the above-mentioned intervention is studied in two randomized groups of pharmacies. One group receives minimal support in the intervention, the other group also receives interactive educational meetings, reminders and feedback, and support of multiprofessional cooperation.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 57
-
pharmacies: resident in the south of the Netherlands
-
patients:
- 18 years or older
- diagnosis of hypertension
- systolic blood pressure between 150 and 180 mm Hg despite the use of antihypertensive drug(s)
- indication for treatment escalation
-
patients:
- impossibility to establish blood pressure properly
- patient treated by medical specialist
- change of antihypertensive therapy because of adverse effects of current medication
- insisting on using dose organisers
- not managing their drug intake themselves
- not able to come to the pharmacy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description max extensive implementation programme - min control -
- Primary Outcome Measures
Name Time Method the number of patients included for intervention 9 months after start of the study
- Secondary Outcome Measures
Name Time Method improvement of systolic blood pressure 2 and 5 months after inclusion treatment escalation of patients after inclusion into the study 5 months after inclusion the percentage of GP's in PTAM that cooperates in the intervention 9 months after start of the study