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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02118350
Other study ID # Pilates
Secondary ID
Status Completed
Phase N/A
First received April 16, 2014
Last updated April 16, 2014
Start date April 2012
Est. completion date December 2013

Study information

Verified date April 2014
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Female
Age group 30 Years to 59 Years
Eligibility 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

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Brazil Federal University of Sao Paulo Santos SP

Sponsors (2)

Lead Sponsor Collaborator
Federal University of São Paulo Fundação de Amparo à Pesquisa do Estado de São Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 Yes
Secondary Heart Rate Heart 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. 16 weeks Yes
Secondary Anxiety Anxiety was analyzed by State-Trait Anxiety Inventory (STAI), before and after trial period. 16 weeks. Yes
Secondary Stress Stress was analysed by perceived stress questionnaire, before and after trial period. 16 weeks Yes
Secondary Depression Depression was analysed by Beck's Depression Inventory (BDI), before and after trial period. 16 weeks Yes
Secondary Sleep quality Sleep quality was analysed by The Pittsburgh Sleep Quality Index (PSQI), before and after trial period. 16 weeks Yes
Secondary Perception of Sleep Perception of Sleep was analysed by Mini Sleep Questionnaire, before and after trial period. 16 weeks Yes
Secondary Sleepiness Sleepiness was analysed by Epworth Sleepiness Scale, before and after trial period. 16 weeks Yes
Secondary Quality of Life Quality of Life was analysed by Questionnaire for Health-Related Quality of Life assessment of hypertensive patients, before and after trial period. 16 weeks Yes
Secondary Flexibility Flexibility was analysed by Bank of wells, before and after trial period. 16 weeks Yes
Secondary Strength Strength was analysed by hydraulic handgrip dynamometer, before and after trial period. 16 weeks Yes
Secondary Body weight 16 weeks Yes
Secondary Height 16 weeks Yes
Secondary Waist circumference 16 weeks Yes
Secondary Hip circumference 16 weeks Yes
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