Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
21 participants
INTERVENTIONAL
2011-10-31
2012-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Pilates and Muscle Strength Respiratory
NCT02189044
Pilates and PNF Methods Induces Similar Strength Gains
NCT02274909
Effects of Pilates Exercises in Asthmatic Patients
NCT03670654
Effects of Respiratory Muscle Training in Obese Women
NCT03767556
Effect of Inspiratory Muscle Training on Posture in Chronic Obstructive Pulmonary Disease Patients
NCT04117399
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The study included women with body mass index (BMI) ≤ 29 kg/m2 were not engaged in regular physical activity, or sedentary lifestyle with scores up to eight, according to Baecke et al., non-smoker, non-alcoholic, without any abnormalities of the cardiovascular, respiratory and neuromuscular.
The study excluded women with disabling diseases, pregnancy, postpartum less than a year, inability to understand the tests and exercises proposed or refuse to participate in the study.
The volunteers, aged between 25 and 55 years, were allocated in to two groups:
1. Pilates Group (n = 16): sedentary volunteers, but that would begin activities with the Pilates method and evaluated three months.
2. Control group (n = 13): sedentary volunteers and remain sedentary and evaluated in three months.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Pilates Group
Sedentary volunteers, but that would begin activities with the Pilates method and evaluated in three months.
Therapeutic intervention in the Pilates method has two regular weekly sessions for 12 weeks, totaling 24 sessions.
For the protocol of Pilates exercises, exercises on soil and equipment, with gradual progression of the load.
Pilates method
Therapeutic intervention in the Pilates method has two regular weekly sessions for 12 weeks, totaling 24 sessions. For the protocol of Pilates exercises, exercises on soil and equipment, with gradual progression of the load.
Control Group
Sedentary volunteers and remain sedentary and evaluated in three months. The volunteers comprised the control group did not perform any physical activity during the study period.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pilates method
Therapeutic intervention in the Pilates method has two regular weekly sessions for 12 weeks, totaling 24 sessions. For the protocol of Pilates exercises, exercises on soil and equipment, with gradual progression of the load.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* not physically active on a regular basis, ie, sedentary lifestyle with scores up to eight, according to Baecke et al.
* nonsmokers
* non-alcoholic
* without any abnormalities in the cardiovascular, respiratory or neuromuscular
Exclusion Criteria
* gestation
* puerperium there is less than a year
* inability to understand the tests and exercises proposed
25 Years
55 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Universidade Metodista de Piracicaba
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Eli Maria Pazzianotto Forti
PhD
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Universidade Metodista de Piracicaba (UNIMEP)
Piracicaba, São Paulo, Brazil
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Pilates2012
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.