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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03907384
Other study ID # 1342019
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2018
Est. completion date October 30, 2018

Study information

Verified date October 2020
Source Marymount University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Obesity is associated with progressive decreases in arterial health and function. It is crucial to prevent or reduce the negative effects of aging on the vasculature by implementing appropriate lifestyle interventions, such as exercise training. We examined the effects of a Mat Pilates training (MPT) regimen on arterial stiffness (pulse wave velocity, PWV), blood pressure (BP), wave reflection (AIx) and endothelial function in obese premenopausal women with elevated BP.


Description:

Using a parallel experimental design, participants were randomly assigned to either MPT (n=14) or non-exercising control group (n=14) for 12 weeks. Participant in the MPT group trained 3 days/week . Participants' brachial to ankle PWV (baPWV), systolic and diastolic BP, AIx, plasma NO levels were measured at baseline and after 20 weeks of their assigned intervention.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date October 30, 2018
Est. primary completion date October 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - body mass index 30-40 kg/m2 - <1 h of regular exercise per week in the previous year - systolic/diastolic BP: 120-129mm Hg systolic BP and ? 80 mm Hg for diastolic BP - Nonsmokers Exclusion Criteria: - body mass index ?30 and =40 kg/m2 - chronic diseases - taking oral contraceptives - pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mat Pilates training
This group completed 12-weeks of training

Locations

Country Name City State
United States University of Nebraska Omaha Nebraska

Sponsors (4)

Lead Sponsor Collaborator
Marymount University Busan University, Texas Tech University, University of Isfahan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Arterial Stiffness via Pulse Wave Velocity 12 weeks
Secondary Systolic and Diastolic Blood Pressure Automatic BP monitor 12 weeks
Secondary Pressure Wave Reflection via Augmentation Index 12 weeks
Secondary Endothelial Function via plasma nitric oxide 12 weeks
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