Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease

Chronic Obstructive Pulmonary Disease Clinical Trial

Official title:

Effect of Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05781867
• Other study ID #: manual therapy in COPD
• Status: Completed
• Phase: N/A
• Start date: March 20, 2023
• Est. completion date: March 1, 2024

Study information

• Verified date: April 2024
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Our study aiming for determining the combined effect of selective manual therapy techniques in chronic obstructive pulmonary disease patients

Description:

I will apply selective manual therapy techniques in form of mobilization techniques ,myofascial release techniques combined with traditional treatment to determine thier effect in chronic obstructive pulmonary disease patients

Recruitment information / eligibility

• Status: Completed
• Enrollment: 52
• Est. completion date: March 1, 2024
• Est. primary completion date: January 1, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 50 Years to 60 Years

Eligibility

Inclusion Criteria:

• All patients must diagnosed mild to moderate chronic obstructive pulmonary disease

• All patients should have foreward head and kyphosis

Exclusion Criteria:

• History of osteoporosis.

• Acute exacerbation.

• Presence of active hemoptysis

• Presence of malignant disease

Related Conditions & MeSH terms

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

Intervention

Other:
• Manual therapy and conventional physical therapy treatment
manual therapy (chest mobilization, diaphragmatic myofascial release, myofascial release for pectoralis minor, pectoralis major, scaleni ),pursed lip breathing, diaphragmatic breathing and active range of motion exercises of upper limbs

Locations

Country	Name	City	State
Egypt	Cairo University	Giza

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	chest expansion	caliper will be used to assess chest expansion into centimeter	pre-intervention and after 8 weeks of intervention
Primary	(the forced vital capacity (FVC), forced expiratory volume at first second (FEV1) and FEV1/FVC will be recorded. )	spirometry used to measure	pre-intervention
Primary	cranio-vertebral angle and kyphotic angle in degrees	kinovea software will be used to assess in degrees	pre-intervention
Primary	functional capacity.	Six minute walk test will be used to assess functional capacity(meter/minutes)	pre-intervention
Primary	dyspnea score	Modified Medical Research Council dyspnea scale (mMRC dyspnea scale) will be used to assess dyspnea	pre-intervention