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Effect of Mat Pilates Training on Blood Pressure of Hypertensive Individuals

Effect of Mat Pilates Training on Blood Pressure of Hypertensive Individuals

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02118350
Enrollment
44
Registered
2014-04-21
Start date
2012-04-30
Completion date
2013-12-31
Last updated
2014-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

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.

Interventions

Mat Pilates training performed two times at week for 16 weeks.

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
Federal University of São Paulo
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 59 Years
Healthy volunteers
No

Inclusion criteria

* Hypertensives women * Age 30 to 59 years * Nonactive * Make use of antihypertensive medication

Exclusion criteria

* Orthopedic problems or other problem that prevented the exercises * Change in drug treatment during protocol * Absence in more than 25% of the exercise sessions

Design outcomes

Primary

MeasureTime frameDescription
Blood pressure16 weeksBlood 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.

Secondary

MeasureTime frameDescription
Heart Rate16 weeksHeart Rate 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.
Anxiety16 weeks.Anxiety was analyzed by State-Trait Anxiety Inventory (STAI), before and after trial period.
Stress16 weeksStress was analysed by perceived stress questionnaire, before and after trial period.
Depression16 weeksDepression was analysed by Beck's Depression Inventory (BDI), before and after trial period.
Sleep quality16 weeksSleep quality was analysed by The Pittsburgh Sleep Quality Index (PSQI), before and after trial period.
Perception of Sleep16 weeksPerception of Sleep was analysed by Mini Sleep Questionnaire, before and after trial period.
Sleepiness16 weeksSleepiness was analysed by Epworth Sleepiness Scale, before and after trial period.
Quality of Life16 weeksQuality of Life was analysed by Questionnaire for Health-Related Quality of Life assessment of hypertensive patients, before and after trial period.
Flexibility16 weeksFlexibility was analysed by Bank of wells, before and after trial period.
Strength16 weeksStrength was analysed by hydraulic handgrip dynamometer, before and after trial period.
Body weight16 weeks
Height16 weeks
Waist circumference16 weeks
Hip circumference16 weeks

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026