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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05781867
Other study ID # manual therapy in COPD
Secondary ID
Status Completed
Phase N/A
First received
Last updated
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
Health authority
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

Study Design


Related Conditions & MeSH terms


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
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