Hypertension Clinical Trial
Official title:
Advanced Practice Nurse Intervention Versus Usual Care for Hypertension Control: Study Protocol for an Open-label Randomized Controlled Trial
Hypertension is the most frequent chronic pathology in France and in the world. It is one of the main modifiable cardiovascular risk factors. In France, 50% of treated hypertensives are uncontrolled and only 30% of treated patients are fully adherent to their antihypertensive treatment. Poor adherence to drug treatments is considered as one of the main causes of non-control of hypertension. Since 2018, a new profession has entered the French healthcare system: Advanced Practice Nurses (APN). They have many broad skills, at the interface of nursing and medical exercises. The purpose of this interventional study is to assess the impact of APN on blood pressure (BP) control in the context of usual care of hypertension thanks to a better adhesion of patients and a better therapeutic alliance. The hypothesis formulated is that an individual APN intervention, included in a usual hypertension management, improves BP control.
Status | Not yet recruiting |
Enrollment | 330 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - at least 18 years of age, - treated or untreated hypertension, - can to provide a written informed consent. Exclusion Criteria: - age under 18 years old, - inability to give a free informed consent. |
Country | Name | City | State |
---|---|---|---|
France | Hôpital Hôtel-Dieu | Paris |
Lead Sponsor | Collaborator |
---|---|
Hotel Dieu University Hospital, France |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of controlled blood pressure in MD consultation (office blood pressure < 140/90 mmHg) | According to the European and International guidelines, the protocol for office BP measurement will be: 5 minutes rest, 3 measurements at one-minute intervals in supine position followed by 3 standing measurements at one-minute intervals for orthostatic hypotension test. Unattended office blood pressure measurement will be conducted thanks to a supervisor (usually a nurse) who will explain the protocol to the patient before letting him rest in a quiet room and thanks to an automatic sphygmomanometer that can print the statement of measures at the end of the monitoring. Blood pressure level will be estimated by the average of the 2 last blood pressure measures in supine position. We will consider that blood pressure is controlled if systolic blood pressure < 140 mmHg and diastolic blood pressure < 90 mmHg. | 12 months | |
Secondary | Rate of home blood pressure monitoring brought to MD consultation | According to the 2020 International Society of Hypertension (ISH) Global Hypertension Practice Guidelines, the protocol for home BP monitoring will be: 3-day monitoring with a cycle of 3 measures every morning and every evening at one-minute intervals, in a sitting position, after 5 minutes of rest and before meals. | 12 months | |
Secondary | Quality of the home blood pressure monitoring brought to MD consultation | The quality will be assessed by the number of measurements (18 measurements over 3 days according to the protocol). | 12 months | |
Secondary | Rate of therapeutic adjustments during the APN intervention | Rate of therapeutic adjustments among the interventional group during the APN intervention. | 6 months | |
Secondary | Indication(s) of therapeutic adjustments during the APN intervention | Rate of therapeutic adjustments due to lack of efficacy and/or intolerance among the interventional group during the APN intervention. | 6 months | |
Secondary | Difference in rates of controlled blood pressure (office blood pressure < 140/90 mmHg) between day hospitalization and MD consultation in each group. | Evolution of the rate of controlled blood pressure between day hospitalization and MD consultation in each group. | 12 months |
Status | Clinical Trial | Phase | |
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