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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04862754
Other study ID # P.T REC/012/003094.
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 25, 2021
Est. completion date April 15, 2021

Study information

Verified date March 2022
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study is aiming to assess the chronic effect of the interval training program on arterial stiffness in women with hypertension


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 15, 2021
Est. primary completion date March 30, 2021
Accepts healthy volunteers No
Gender Female
Age group 40 Years to 60 Years
Eligibility Inclusion Criteria: - physically inactive - BMI 30-40 - Stage 1 and 2 hypertension - Elevated BP as systolic BP =130 mm Hg and/or diastolic BP =85 mm Hg measured at the brachial artery. Exclusion Criteria: - Medications known to affect weight or appetite - Any disease associated with exercise intolerance. - Women were taking hormone replacement therapy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
interval training exercise
interval training exercise

Locations

Country Name City State
Egypt Faculty of physical therapy Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Central arterial stiffness measurements (Pulse Wave Velocity [PWV], augmentation index ) Pulse wave analysis (PWA) of the women in the two groups: pre and post treatment for pulse wave velocity (PWV) and augmentation index(AIx)
Pulse Wave Velocity [PWV], augmentation index (AIx @75HR) and resting heart rate were measured using analysis equipment which called Non-invasive blood pressure measurement system using "Mobil-O-Graph 24h PWA " with Hypertension Management Software Client Server (HMS-CS 4.3). PWA was performed using an oscillometric Mobil-O-Graph R 24 h PWA Monitor device (I.E.M GmbH, Germany) with integrated ARCSolverĀ® software
two months
Secondary blood lipid profile blood analysis will be used to measure lipid profile (high and low-density lipoprotein, cholesterol, triglyceride) two months
Secondary interleukin 6 blood analysis will be used to measure interleukin 6 two months
Secondary blood pressure (systolic and diastolic) resting Blood pressure was monitored from the right arm using an automated digital electronic BP monitor (Omron digital BP monitor, Model 11 EM 403c; Tokyo Japan). two months
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