Back to resultsCardiorespiratory Training and Ventilatory Muscle Strength (RMS)
Primary Purpose
Sarcopenia
Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Cardiorespiratory training
ventilatory training
Sponsored by
About this trial
This is an interventional treatment trial for Sarcopenia
Eligibility Criteria
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.
Sites / Locations
- Gama Filho University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
No Intervention
Arm Label
Cardiorespiratory training
Ventilatory Training
Crontrol Group
Arm Description
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 ventilatory training group will undergo 18 sessions, periodized in a maximum six weeks, respecting the minimum weekly frequency of three sessions.
This condition will last six weeks, this period will be held six lectures sixty minutes long and periodization weekly.
Outcomes
Primary Outcome Measures
Ventilatory muscle strength
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).
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01912482
Brief Title
Cardiorespiratory Training and Ventilatory Muscle Strength
Acronym
RMS
Official Title
Chronic Effect of Cardiorespiratory Training on Ventilatory Muscle Strength in Elderly Women: Controlled Trial, Randomized and Double Blind.
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Unknown status
Study Start Date
July 2015 (undefined)
Primary Completion Date
June 2016 (Anticipated)
Study Completion Date
December 2016 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Gama Filho
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The cardiorespiratory training can increase muscle strength ventilatory.
Detailed Description
Specifically for being an experiment parallel factorial intervention after met the eligibility criteria for the participants will be randomly allocated to three groups: control, respiratory training, cardiorespiratory training (indoor Bike).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcopenia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Cardiorespiratory training
Arm Type
Experimental
Arm Description
The cardiorespiratory training group will undergo 18 sessions, these also periodized in a maximum six weeks, respecting the minimum weekly frequency of 3 sessions.
Arm Title
Ventilatory Training
Arm Type
Active Comparator
Arm Description
The ventilatory training group will undergo 18 sessions, periodized in a maximum six weeks, respecting the minimum weekly frequency of three sessions.
Arm Title
Crontrol Group
Arm Type
No Intervention
Arm Description
This condition will last six weeks, this period will be held six lectures sixty minutes long and periodization weekly.
Intervention Type
Other
Intervention Name(s)
Cardiorespiratory training
Other Intervention Name(s)
GTC
Intervention Description
The cardiorespiratory training group will undergo 18 sessions, these also periodized in a maximum six weeks, respecting the minimum weekly frequency of 3 sessions.
Intervention Type
Other
Intervention Name(s)
ventilatory training
Other Intervention Name(s)
GTV
Intervention Description
The ventilatory training group will undergo 18 sessions, periodized in a maximum six weeks, respecting the minimum weekly frequency of three sessions.
Primary Outcome Measure Information:
Title
Ventilatory muscle strength
Description
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).
Time Frame
The ventilatory muscle strength (MIP and MEP) will be measured after 18 cardiorespiratory training sessions held in 6 weeks.
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fabio D Pereira, MSc
Phone
552178705024
Email
profabiodutra@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Elirez B Silva, Doctoral
Phone
552125997170
Email
elirezsilva@ugf.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fabio D Pereira, MSc
Organizational Affiliation
Gama Filho University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gama Filho University
City
Rio de Janeiro
State/Province
RJ
ZIP/Postal Code
23050-260
Country
Brazil
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fabio D Pereira, MSc
Phone
552178705024
Email
profabiodutra@hotmail.com
First Name & Middle Initial & Last Name & Degree
Elirez B Silva, Doctoral
Phone
552125997170
Email
elirezsilva@ugf.com
First Name & Middle Initial & Last Name & Degree
Fabio D Pereira, MSc
12. IPD Sharing Statement
Learn more about this trial
Cardiorespiratory Training and Ventilatory Muscle Strength
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