Effect of Mat Pilates Training on Blood Pressure of Hypertensive Individuals
1 other identifier
interventional
44
1 country
1
Brief Summary
The study aimed to evaluate the chronic effects of Mat Pilates Training on blood pressure, heart rate, double product and psychobiological factors in hypertensive medicated women and acute effects of Mat Pilates Exercise on blood pressure of such individuals.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable hypertension
Started Apr 2012
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2013
CompletedFirst Submitted
Initial submission to the registry
April 16, 2014
CompletedFirst Posted
Study publicly available on registry
April 21, 2014
CompletedApril 21, 2014
April 1, 2014
1.7 years
April 16, 2014
April 16, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
Blood pressure
Blood pressure was measured by Ambulatorial Monitoring Blood Pressure before and after trial period and by semiautomatic monitoring before and after a single session of Mat Pilates exercise.
16 weeks
Secondary Outcomes (14)
Heart Rate
16 weeks
Anxiety
16 weeks.
Stress
16 weeks
Depression
16 weeks
Sleep quality
16 weeks
- +9 more secondary outcomes
Study Arms (2)
Mat Pilates training
EXPERIMENTALMat Pilates training performed two times at week for 16 weeks.
Control
NO INTERVENTIONInterventions
Mat Pilates training performed two times at week for 16 weeks.
Eligibility Criteria
You may qualify if:
- Hypertensives women
- Age 30 to 59 years
- Nonactive
- Make use of antihypertensive medication
You may not qualify if:
- Orthopedic problems or other problem that prevented the exercises
- Change in drug treatment during protocol
- Absence in more than 25% of the exercise sessions
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Federal University of Sao Paulo
Santos, São Paulo, 11060-001, Brazil
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
April 16, 2014
First Posted
April 21, 2014
Study Start
April 1, 2012
Primary Completion
December 1, 2013
Study Completion
December 1, 2013
Last Updated
April 21, 2014
Record last verified: 2014-04