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Respiratory Resistance Training on Sleep Quality in Persons With Spinal Cord Injury

T

Texas State University, San Marcos

Status

Terminated

Conditions

Spinal Cord Injury

Treatments

Device: Powerlung Performer

Study type

Interventional

Funder types

Other

Identifiers

NCT00629850
TexasState 2008-29541
IRB# 2008-29541 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to determine if the use of a respiratory resistance trainer will increase respiratory muscle strength, improve sleep quality and improve quality of life in individuals with spinal cord injury.

Hypothesis: Use of the respiratory resistance trainer will improve respiratory muscle strength, improve sleep quality, and improve quality of life among individuals with spinal cord injury.

Full description

Individuals with spinal cord injury experience varying degrees of reduced muscle function. Those individuals with high level spinal cord injury, cervical region, may experience reduced diaphragm function. This reduction in function may affect daytime activities as well as sleep quality. Sleep quality in people with spinal cord injury is considered to be worse than sleep quality in the general population. The use of respiratory resistance training devices has been shown to increase muscle strength in people with spinal cord injury. There have been not studies to document potential improvements in sleep quality among individuals with spinal cord injury following respiratory resistance training.

Enrollment

1 patient

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • tetraplegia
  • quadriplegia

Exclusion criteria

  • NA

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

1 participants in 2 patient groups

Powerlung Performer
Experimental group
Description:
The arm will receive the lung trainer device to use for 10 weeks
Treatment:
Device: Powerlung Performer
Control
No Intervention group
Description:
Control. This arm will not receive any device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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