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The Impact of Inspiratory Muscle Strength Training (IMT)

F

Fooyin University

Status

Completed

Conditions

Ventilator Dependency

Treatments

Device: inspiratory muscle strength training

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The study is a pre-post test with quasi experimental design. Forty-two intubated-adults who had been mechanically ventilated for more than 21 days were selected on the basis of inclusion criteria in respiratory care ward. These patients were classified equally into study group and control group. The experimental group received the intervention of respiratory muscles training 5 times/ a week for 6 weeks. The control group received normal care. The intervention was adjusted trigger sensitivity to 10% of the first recorded Maximal Inspiratory Pressure at the start of training, then increased the ventilator trigger sensitivity and training duration weekly. The largest of ventilator trigger sensitivity is not over 40% of the initial Maximal Inspiratory Pressure and the timing of training duration is no longer than 30 minutes.

Enrollment

43 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age >20y/o
  • Vital signs stable
  • MIP <20cmH2O
  • Ventilator FiO2<40%, PEEP <8
  • Ventilator mode:PSV or SIMV

Exclusion criteria

  • Patient or family refuse

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

43 participants in 2 patient groups

Control group
No Intervention group
Description:
as usual care
experimental group
Experimental group
Description:
The intervention of inspiratory muscle strength training
Treatment:
Device: inspiratory muscle strength training

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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