Sexual Dysfunction in Hypertensive Women
NCT05156385 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 348
Last updated 2024-10-23
Summary
Several studies describe the existence of an association between sexual dysfunction and high blood pressure (hypertension), most often characterized by a decrease in the number of orgasms and the existence of dyspareunia.
Hypertension is a contributing factor, and nonadherence to medication could amplify it.
There are several ways to assess adherence to treatment: the use of declarative questionnaires, a method not without criticism because it is subject to the subjectivity of the declaration by the patient; and drug dosages, a standard technique, although insufficiently disseminated due to the high cost and greater weight of the survey protocols. Drug non-compliance is multifactorial. In addition, it has been shown that having undesirable drug effects and / or being afraid of developing them is one of the major causes of non-compliance with antihypertensive treatments.
The investigators hypothesize that DS is significantly more common among hypertensive women treated with non-observers compared to hypertensive women treated with observers.
The main objective is to compare the prevalence of sexual dysfunction between a group of hypertensive women treated as observers and a group of hypertensive women treated as non-observers.
Conditions
Interventions
- BIOLOGICAL
-
Blood sample for the determination of antihypertensives or their metabolites.
15 ml of Blood sample for the determination of antihypertensives or their metabolites
- BEHAVIORAL
-
Questionnaire on sexual activity
Questionnaire on sexual activity in women
- BEHAVIORAL
-
Scale on hospital anxiety and depression
Scale on hospital anxiety and depression to detect anxious and depressive symptoms (14 questions)
- BEHAVIORAL
-
Morisky Questionaire
anti-hypertensive medication compliance questionnaire
Sponsors & Collaborators
-
University Hospital, Toulouse
lead OTHER
Principal Investigators
-
Delphine LAZARO-VERGE, MD · University Hospital, Toulouse
Study Design
- Allocation
- NA
- Purpose
- HEALTH_SERVICES_RESEARCH
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-06-27
- Primary Completion
- 2026-07-07
- Completion
- 2026-07-07
Countries
- France
Study Locations
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