Skip to main content
Clinical Trials/NCT05876403
NCT05876403
Completed
Not Applicable

Effects of Respiratory Proprioceptive Neuromuscular Facilitation (PNF) Technique on Pulmonary Function of Chronic Pulmonary Obstructive Disease (COPD) Patients.

Riphah International University1 site in 1 country56 target enrollmentSeptember 1, 2023
ConditionsCOPD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COPD
Sponsor
Riphah International University
Enrollment
56
Locations
1
Primary Endpoint
Forced expiratory volume in 1sec (FEV1)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the impact of PNF technique combined with aerobic exercises among COPD patients in a clinical setting. Previous literature has evaluated this technique in ventilated patients but in clinical setting specifically in Pakistan, this invention therapy has not been implied in COPD patients.

Detailed Description

Chronic Obstructive Pulmonary Disorder manifested as breathlessness, respiratory difficulties and persistent cough is one of the biggest causes of mortality around the world. 2.1% of Pakistani population has COPD. Proprioceptive neuromuscular facilitation is used as management technique in which muscle stretching promotes chest wall mobility and restores regular breathing rhythm. In previous studies, PNF technique combined with aerobic exercises has been utilized to improve Pulmonary functions in COPD patients. But the sample size of these studies was small and participants were ventilated patients, hence not targeting the diaphragm. Our study shall evaluate the impact of PNF technique combined with aerobic training on the Pulmonary function of COPD patients in the clinical setting.

Registry
clinicaltrials.gov
Start Date
September 1, 2023
End Date
December 15, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Both male \& female participants.
  • Diagnosed COPD patients
  • Age 35-60years
  • Ratio of forced expiratory volume in first second \& forced vital capacity(FEV1/FVC \<0.7,30%\<FEV1\<80%
  • Stable clinical condition.

Exclusion Criteria

  • Serious conditions with require supplementary oxygen or ventilator/support devices.
  • COPD exacerbation within last 4weeks
  • Patients with recent chest wall trauma, surgery or deformity.
  • Patient with neurological, psychological, musculoskeletal, or cardiac medical history.
  • Pulmonary disease with physical impairment.
  • Inability to follow the pulmonary rehabilitation program.

Outcomes

Primary Outcomes

Forced expiratory volume in 1sec (FEV1)

Time Frame: two weeks

Forced expiratory volume in 1sec (FEV1) measured through digital spirometer. If the value of FEV1 is within 80% of the reference value, the results are considered normal

Chest Expansion

Time Frame: two weeks

The expansion of chest during breathing will be measures and axillary, nipple and xiphisternal level using a measuring tape.

Modified Borg Dyspnea Scale

Time Frame: two weeks

Participants will fill this 12 points Scale to show breathing difficulty from 0 to 10.

COPD assessment test

Time Frame: two weeks

8 points questionnaire will evaluate patients Pulmonary function capacity through semantic 6 point difference Scale.

Peak expiratory flow rate (PEFR)

Time Frame: two weeks

Peak expiratory flow rate (PEFR) Peak expiratory flow rate (PEFR) measured through digital spirometer. Peak Expiratory Flow Rate (PEFR) measured through digital spirometer. Three zones of measurement are commonly used to interpret peak flow rates. Normal value of PEFR is (80-100%). Green zone indicates 80 to 100 percent of the usual or normal peak flow reading, yellow zone indicates 50 to 79 percent of the usual or normal peak flow readings, and red zone indicates less than 50 percent of the usual or normal peak flow readings.

Forced vital capacity (FVC)

Time Frame: two weeks

Forced vital capacity (FVC) measured through digital spirometer. If the value of FVC is within 80% of the reference value, the results are considered normal. Changes in FVC from baseline to 5th and after 15th day of intervention will be assessed.

Secondary Outcomes

  • 6 minutes walk test:(two weeks)

Study Sites (1)

Loading locations...

Similar Trials