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Clinical Trial Summary

This study evaluate the feasibility of a 6-month personalized support program for hypertensive and non-observant women, led by nurses by telephone follow-up.


Clinical Trial Description

The program includes 2 themes:

1. "Realizing my blood pressure self-measurement" according to the recommendations

2. "Optimizing my compliance": understand the antihypertensive treatment, identify the brakes and the levers when taking medication, organize the treatment taking

Visits :

1. Inclusion visit :

- Collection of consent by the nurse

- Verification of inclusion and non-inclusion criteria : measurement of compliance with a scale for each antihypertensive treatment and BP measurement

- Data collection and goal setting

- Urine collection for dosing anti-hypertension drugs

- Delivery of the schedule of telephone visits that were determined with the patient

2. Implementation of personalized support with the following steps :

- Data collection : evaluate knowledge and its potential as a patient, identify his needs

- Determination of objectives : define the objectives of the program in each theme with the patient according to the collection of data Implementation of personalized support

- 7 telephone interviews of 20 to 30 minutes use of specific teaching tools and materials by thematic assessment of achievements, validation of objectives

Evaluation of the accompaniment:

- assessment at the final visit

3. Final visit at 6-month : Same as the inclusion visit with assessment of the support and questionnaire to assess the patient satisfaction level. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03963934
Study type Interventional
Source Central Hospital, Nancy, France
Contact Edith DAUCHY, RN
Phone 33 3 83 15 73 13
Email e.dauchy@chru-nancy.fr
Status Not yet recruiting
Phase N/A
Start date December 1, 2019
Completion date June 1, 2021

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