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Mat Pilates and Vascular Function in Obese Females

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03907384
Recruitment Status : Completed
First Posted : April 9, 2019
Last Update Posted : October 30, 2020
Sponsor:
Collaborators:
Busan University
Texas Tech University
University of Isfahan
Information provided by (Responsible Party):
Alexei Wong, Marymount University

Brief 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.

Condition or disease Intervention/treatment Phase
Obese Elevated Blood Pressure Behavioral: Mat Pilates training Not Applicable

Detailed 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.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 28 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: The Effects of Mat Pilates Training on Vascular Function in Obese Premenopausal Women With Elevated Blood Pressure
Actual Study Start Date : April 1, 2018
Actual Primary Completion Date : October 30, 2018
Actual Study Completion Date : October 30, 2018

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Mat Pilates training
The MPT group participated in 3-one hour supervised training sessions per week for 12 weeks. All MP sessions were performed in nonconsecutive days. The MP sessions were divided into the following stages: initial warm up and stretching (10 min), general conditioning consisting of MP exercises (40 min) and stretching and cooling down (10 min). The participants performed 12 basic MP exercises (one set of 6-10 repetitions was performed per exercise). Breathing, a core principle of MP, was performed by forced but controlled inspirations and exhalations, while relaxing and contracting the abdomen, respectively. All sessions were supervised by a certified MP instructor.
Behavioral: Mat Pilates training
This group completed 12-weeks of training

No Intervention: Control
Participants in the non-exercising control group did not participate in a supervised exercise program and visited the laboratory at the same frequency as participants in the swim intervention and underwent recreational activities such as board games



Primary Outcome Measures :
  1. Arterial Stiffness [ Time Frame: 12 weeks ]
    via Pulse Wave Velocity


Secondary Outcome Measures :
  1. Systolic and Diastolic Blood Pressure [ Time Frame: 12 weeks ]
    Automatic BP monitor

  2. Pressure Wave Reflection [ Time Frame: 12 weeks ]
    via Augmentation Index

  3. Endothelial Function [ Time Frame: 12 weeks ]
    via plasma nitric oxide



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 35 Years   (Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Accepts Healthy Volunteers:   Yes
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03907384


Locations
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United States, Nebraska
University of Nebraska
Omaha, Nebraska, United States, 68022
Sponsors and Collaborators
Marymount University
Busan University
Texas Tech University
University of Isfahan
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Alexei Wong, Assistant Professor, Marymount University
ClinicalTrials.gov Identifier: NCT03907384    
Other Study ID Numbers: 1342019
First Posted: April 9, 2019    Key Record Dates
Last Update Posted: October 30, 2020
Last Verified: October 2020

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Hypertension
Vascular Diseases
Cardiovascular Diseases