Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-25 @ 2:28 AM
Ignite Modification Date:
2025-12-25 @ 2:28 AM
NCT ID:
NCT03963934
Brief 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.
Detailed 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:
NCT03963934
Study Brief:
Protocol Section:
NCT03963934