Chronic Obstructive Pulmonary Diseases and Proprioceptive Neuromuscular Facilitation

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:

The Effect of Resistant Proprioceptive Neuromuscular Facilitation Exercises on Respiratory Muscle Strength in Chronic Obstructive Pulmonary Diseases

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05723302
• Other study ID #: IstanbulMUH_1999
• Status: Completed
• Phase: N/A
• Start date: January 20, 2017
• Est. completion date: December 1, 2022

Study information

• Verified date: February 2023
• Source: Istanbul Medipol University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To investigate the effects of resistant proprioceptive neuromuscular facilitation exercises on physical fitness, respiratory muscle strength, walking distance and quality of life in chronic obstructive pulmonary patients.

Description:

The study was carried out between January 2017 and January 2019, with patients followed up with the diagnosis of COPD in Çanakkale Mehmet Akif Ersoy State Hospital and Çanakkale Onsekiz Mart University Medical Faculty Hospital, Department of Chest Diseases. It was approved by Istanbul Medipol University Non-Interventional Clinical Research Ethics Committee (Date: 30.12.2016, Decision No. 573) and was done in accordance with the Declaration of Helsinki. All participants were informed about the purpose of the study, the total duration of treatment and the applications to be made, and a consent form was signed. The study was conducted as a prospective and randomized controlled study, and inclusion and exclusion criteria were determined.

Thirty-five patients diagnosed with COPD were referred to the study, four patients were excluded because they did not meet the inclusion criteria, and the study was conducted with a total of 31 participants.

The 31 patients included in the study were randomized after their initial evaluation and divided into two groups as experimental and control groups. Patients meeting the inclusion criteria were divided into 2 groups. Randomized by ordering by date of application.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: December 1, 2022
• Est. primary completion date: March 17, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 38 Years to 67 Years

Eligibility

Inclusion Criteria:

• To be diagnosed with stage 1, stage 2 and stage 3 COPD according to GOLD (Global Initiative for Obstructive Lung Diseases) criteria

• Having FEV1/FVC <70% according to pulmonary function test

• Being clinically stable

• Being over 18 years old

• Volunteer to participate in the program

Exclusion Criteria:

• Having a COPD exacerbation in the last 8 weeks

• To have participated in a regular exercise training program in the last 1 year

• Having a musculoskeletal disease and neuromuscular disease that may prevent exercise

• Inability to cooperate for pulmonary function test and respiratory muscle strength measurement

• Being on long-term oxygen therapy

Related Conditions & MeSH terms

• Chronic Obstructive Pulmonary Disease
• Lung Diseases
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive

Intervention

Diagnostic Test:
• MIP/MEP
MIP/MEP

Locations

Country	Name	City	State
Turkey	Çanakkale Onsekiz Mart University	Çanakkale
Turkey	Mehmet Akif Ersoy State Hospital	Çanakkale

Sponsors (3)

Lead Sponsor	Collaborator
Istanbul Medipol University Hospital	Çanakkale Onsekiz Mart University, Mehmet Akif Ersoy Canakkale State Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	HADS	Hospital Anxiety Depression Scale	10 minutes
Secondary	SGRQ	St George's Respiratory Questionnaire	15 minutes