Incentive Spirometer and Inspiratory Muscle Trainer

NCT ID: NCT05201742

Last Updated: 2022-02-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

18 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-02-06

Study Completion Date

2018-05-10

Brief Summary

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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

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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.

Conditions

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Parkinson Disease

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Inspiratory muscle trainer

Inspiratory muscle trainer group - Inspiratory muscle training was performed.

Group Type ACTIVE_COMPARATOR

Inspiratory muscle training

Intervention Type OTHER

Threshold inspiratory muscle training was performed for 6 weeks with device.

Incentive spirometer

Incentive spirometer group - Incentive spirometry was performed.

Group Type ACTIVE_COMPARATOR

Incentive Spirometry

Intervention Type OTHER

Incentive spirometry was performed for 6 weeks with device.

Interventions

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Inspiratory muscle training

Threshold inspiratory muscle training was performed for 6 weeks with device.

Intervention Type OTHER

Incentive Spirometry

Incentive spirometry was performed for 6 weeks with device.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients diagnosed as having Parkinsonism Disease by the Neuro physician.
* Duration of Parkinson's Disease ≥ 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.
Minimum Eligible Age

65 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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King Saud University

OTHER

Sponsor Role lead

Responsible Party

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Masood Khan

Researcher

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Masood Khan, M.P.Th

Role: PRINCIPAL_INVESTIGATOR

King Saud University

Locations

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King Saud University

Riyadh, , Saudi Arabia

Site Status

Countries

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Saudi Arabia

Other Identifiers

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GSITESC/24/16

Identifier Type: -

Identifier Source: org_study_id

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