- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01912482
Cardiorespiratory Training and Ventilatory Muscle Strength (RMS)
Chronic Effect of Cardiorespiratory Training on Ventilatory Muscle Strength in Elderly Women: Controlled Trial, Randomized and Double Blind.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Elirez B Silva, Doctoral
- Phone Number: 552125997170
- Email: elirezsilva@ugf.com
Study Contact Backup
- Name: Fabio D Pereira, MSc
- Phone Number: 552178705024
- Email: profabiodutra@hotmail.com
Study Locations
-
-
RJ
-
Rio de Janeiro, RJ, Brazil, 23050-260
- Gama Filho University
-
Contact:
- Elirez B Silva, Doctoral
- Phone Number: 552125997170
- Email: elirezsilva@ugf.com
-
Contact:
- Fabio D Pereira, MSc
- Phone Number: 552178705024
- Email: profabiodutra@hotmail.com
-
Principal Investigator:
- Fabio D Pereira, MSc
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Have lower maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) values normative reference proposed by the Brazilian Society of Thoracic.
Exclusion Criteria:
- Not be voluntary to the present study.
- Conditions that oblige participants are absent for more than two weeks of activities performed in the experiment.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Cardiorespiratory training
The cardiorespiratory training group will undergo 18 sessions, these also periodized in a maximum six weeks, respecting the minimum weekly frequency of 3 sessions.
|
The cardiorespiratory training group will undergo 18 sessions, these also periodized in a maximum six weeks, respecting the minimum weekly frequency of 3 sessions.
Other Names:
|
Active Comparator: Ventilatory Training
The ventilatory training group will undergo 18 sessions, periodized in a maximum six weeks, respecting the minimum weekly frequency of three sessions.
|
The ventilatory training group will undergo 18 sessions, periodized in a maximum six weeks, respecting the minimum weekly frequency of three sessions.
Other Names:
|
No Intervention: Crontrol Group
This condition will last six weeks, this period will be held six lectures sixty minutes long and periodization weekly.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ventilatory muscle strength
Time Frame: The ventilatory muscle strength (MIP and MEP) will be measured after 18 cardiorespiratory training sessions held in 6 weeks.
|
The MIP and MEP are measured by a digital manometer 300(BRAZIL). During the measurement the participants should be seated in a chair type office allowing your upper body to remain in contact with the back of it, forming an angle of 90° to the hip, the arms extended along the body, knees flexed too 90° and feet flat on the floor. Participants will use a nose clip. The evaluator will manually compress the face of the participant not allowing the contraction of the buccinator muscles increase intraoral pressure and interfere with the measurement result. In the measurement of MIP participants should hold a maximum inspiration from residual volume (RV) and MEP maximum exhalation from total lung capacity (TLC). |
The ventilatory muscle strength (MIP and MEP) will be measured after 18 cardiorespiratory training sessions held in 6 weeks.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Fabio D Pereira, MSc, Gama Filho University
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BR20132014
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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