MedPath

Incentive Spirometer and Inspiratory Muscle Trainer

Not Applicable
Completed
Conditions
Parkinson Disease
Interventions
Other: Incentive Spirometry
Other: Inspiratory muscle training
Registration Number
NCT05201742
Lead Sponsor
King Saud University
Brief Summary

Patients suffering from parkinsonism have respiratory function abnormalities. This study compared the effects of incentive spirometer and inspiratory muscle trainer on pulmonary functions in patients with parkinsonism.

Detailed Description

The participants were recruited according to the inclusion and exclusion criteria. Participants were divided into two groups - incentive spirometer and inspiratory muscle trainer. These trainings were performed for 6 weeks duration. Several outcome measures related to pulmonary function tests were measured before and after the intervention.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
18
Inclusion Criteria
  • Patients diagnosed as having Parkinsonism Disease by the Neuro physician.
  • Duration of Parkinson's Disease β‰₯ 5 years.
  • Patients with the age of 65 to 80 years.
  • Hoen and Yahr classification within 1 to 3.
  • Both males and females were included.
  • Patients who were able to comprehend the commands.
  • Patients who were willing to participate.
Exclusion Criteria
  • Patients having any cardiovascular and pulmonary disorders.
  • History of smoking currently or in the past.
  • Psychological Impairment.
  • Insufficient verbal/intellectual understanding.
  • Patients with unstable vital parameters.
  • Those unable to perform pulmonary function tests (PFT) because of anatomical abnormalities or clinical signs of dementia.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Incentive spirometerIncentive SpirometryIncentive spirometer group - Incentive spirometry was performed.
Inspiratory muscle trainerInspiratory muscle trainingInspiratory muscle trainer group - Inspiratory muscle training was performed.
Primary Outcome Measures
NameTimeMethod
Forced vital capacity (FVC)6 weeks

Forced vital capacity was measured.

Maximum inspiratory pressure (MIP)6 weeks

Maximum inspiratory pressure was measured.

6-minute walk distance (6 MWD)6 weeks

Distance walked by the patients in 6 minutes was measured.

Forced expiratory volume in 1 second (FEV1)6 weeks

Forced expiratory volume in 1 second was measured

Peak Expiratory Flow Rate (PEFR)6 weeks

Peak Expiratory Flow Rate was measured

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

King Saud University

πŸ‡ΈπŸ‡¦

Riyadh, Saudi Arabia

Β© Copyright 2025. All Rights Reserved by MedPath