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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02636296
Other study ID # HI017/2010
Secondary ID
Status Completed
Phase N/A
First received December 14, 2015
Last updated December 18, 2015
Start date August 2010
Est. completion date July 2012

Study information

Verified date December 2015
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of the present study was to investigate the effects of 12-week Pilates-inspired exercise on functional performance in community-dwelling older women.


Description:

Pilates is an exercise system developed over 70 years ago that has been recently received attention due to its beneficial effects on postural stability, coordination, muscle strength and flexibility. The studies published involving Pilates were very different among them regarding intervention period (5, 8, 12 and 24 weeks), frequency (2 and 3 sessions/week) and exercises (mat, mat with accessories, apparatus and others combinations), making meaningful comparison difficult. Furthermore, other important physical features to maintain an independent life at older age, such as cardiorespiratory fitness, were accessed in few studies. So, the effective benefits of Pilates method on physical fitness of community-dwelling older people remain unclear.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date July 2012
Est. primary completion date June 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 60 Years to 80 Years
Eligibility Inclusion Criteria:

- good health based on clinical examination (doctor's certificate)

- good functional capacity(physical examination)

Exclusion Criteria:

- current smokers

- obese (BMI >30 Kg/cm2)

- musculoskeletal limitations

- neurologic diseases

- cardiovascular diseases

- condition that contraindicated exercise

- regularly engaged in other physical conditioning program (>2x/week and/or >150min/week)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Pilates
The Pilates program was conducted twice weekly, 60 minutes/session, for twelve consecutive weeks by a certified Pilates Instructor.
Control
The control group did not receive the Pilates training program and were instructed to maintain their currently activities during the twelve-week follow-up period.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
University of Sao Paulo Federal University of São Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary physical fitness In this study, physical fitness includes strength, balance and aerobic resistance. changes from baseline physical fitness at 12 weeks No
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