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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05516173
Other study ID # santémilitaire10
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 15, 2022
Est. completion date January 15, 2023

Study information

Verified date August 2022
Source General Administration of Military Health, Tunisia
Contact Aymen NOAMEN, MD
Phone +21620215773
Email no.aymen@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Our study aims to evaluate the role of depression in blood pressure control in ambulatory hypertensive patients.


Description:

Research Problem: Hypertension is a multifactorial disease that affects approximately one quarter of the adult population. It is a major risk factor for stroke and cardiovascular disease. Environmental and psychosocial factors play an important role in hypertension onset and control. The prevalence of depression among hypertensive patients is 26, 8% and its presence is associated with increased risk of cardiovascular-related morbi-mortality. Our study aims to evaluate the role of depression in blood pressure control in ambulatory hypertensive patients. Investigative process: This study is a cross-sectional, multicentric and descriptive study. the investigators intend to include three hundred and two patients. After obtaining their consent, a 24 hour ambulatory blood pressure monitor will be used to evaluate blood pressure control. Depression was assessed by the 9-item-Patient Health Questionnaire (PHQ-9) in Tunisian dialect. Clinical, socio-environmental, psychosocial and therapeutic and prognosis data will be collected from medical records.


Recruitment information / eligibility

Status Recruiting
Enrollment 302
Est. completion date January 15, 2023
Est. primary completion date November 15, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Patients consulting for high blood pressure - Patients older than 18 years. - Patients able to give informed consent. Non inclusion Criteria : - Patients followed for depression under treatment. - Hospitalized patients Exclusion Criteria: - a white coat hypertension

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Blood Pressure Monitoring, Ambulatory
To monitor the blood pressure during 24 hours.

Locations

Country Name City State
Tunisia Regional hospital of Ben Arous Ben Arous
Tunisia Interior Security Forces Hospital La Marsa Tunis
Tunisia Tahar Sfar regional hospital of Mahdia Mahdia
Tunisia Military Hospital of Tunis Tunis

Sponsors (1)

Lead Sponsor Collaborator
General Administration of Military Health, Tunisia

Country where clinical trial is conducted

Tunisia, 

References & Publications (1)

Li Z, Li Y, Chen L, Chen P, Hu Y. Prevalence of Depression in Patients With Hypertension: A Systematic Review and Meta-Analysis. Medicine (Baltimore). 2015 Aug;94(31):e1317. doi: 10.1097/MD.0000000000001317. Review. Erratum in: Medicine (Baltimore). 2018 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary prevalence of depression in uncontrolled hypertensive patients. The prevalence of depression evaluated by PHQ9 in Tunisian dialect in hypertensive patients with abnormal ambulatory 24 hours blood pressure monitoring on inclusion
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