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Cardiorespiratory Training and Ventilatory Muscle Strength (RMS)

U

Universidade Gama Filho

Status

Unknown

Conditions

Sarcopenia

Treatments

Other: ventilatory training
Other: Cardiorespiratory training

Study type

Interventional

Funder types

Other

Identifiers

NCT01912482
BR20132014

Details and patient eligibility

About

The cardiorespiratory training can increase muscle strength ventilatory.

Full 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).

Enrollment

30 estimated patients

Sex

Female

Ages

60 to 79 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 3 patient groups

Cardiorespiratory training
Experimental group
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.
Treatment:
Other: Cardiorespiratory training
Ventilatory Training
Active Comparator group
Description:
The ventilatory training group will undergo 18 sessions, periodized in a maximum six weeks, respecting the minimum weekly frequency of three sessions.
Treatment:
Other: ventilatory training
Crontrol Group
No Intervention group
Description:
This condition will last six weeks, this period will be held six lectures sixty minutes long and periodization weekly.

Trial contacts and locations

1

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Central trial contact

Fabio D Pereira, MSc; Elirez B Silva, Doctoral

Data sourced from clinicaltrials.gov

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