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Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Manual therapy and conventional physical therapy treatment
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease

Eligibility Criteria

50 Years - 60 Years (Adult)MaleAccepts Healthy Volunteers

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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Experimental

    Arm Label

    control

    manual therapy

    Arm Description

    26patients will be included in this group and will receive conventional physiotherapy in form of pursed lip breathing, diaphragmatic breathing exercise and Active Range of Motion of both upper extremities

    26patients will be included in this group and will receive manual therapy (chest mobilization, diaphragmatic myofascial release, myofascial release for pectoralis minor and major, scaleni ) and conventional physiotherapy

    Outcomes

    Primary Outcome Measures

    chest expansion
    caliper will be used to assess chest expansion into centimeter
    (the forced vital capacity (FVC), forced expiratory volume at first second (FEV1) and FEV1/FVC will be recorded. )
    spirometry used to measure
    cranio-vertebral angle and kyphotic angle in degrees
    kinovea software will be used to assess in degrees
    functional capacity.
    Six minute walk test will be used to assess functional capacity(meter/minutes)
    dyspnea score
    Modified Borg scale will be used to assess dyspnea

    Secondary Outcome Measures

    Full Information

    First Posted
    January 21, 2023
    Last Updated
    March 22, 2023
    Sponsor
    Cairo University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05781867
    Brief Title
    Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease
    Official Title
    Effect of Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    June 1, 2023 (Anticipated)
    Primary Completion Date
    March 1, 2024 (Anticipated)
    Study Completion Date
    May 1, 2024 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Cairo University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

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

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Obstructive Pulmonary Disease

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    52 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    control
    Arm Type
    Placebo Comparator
    Arm Description
    26patients will be included in this group and will receive conventional physiotherapy in form of pursed lip breathing, diaphragmatic breathing exercise and Active Range of Motion of both upper extremities
    Arm Title
    manual therapy
    Arm Type
    Experimental
    Arm Description
    26patients will be included in this group and will receive manual therapy (chest mobilization, diaphragmatic myofascial release, myofascial release for pectoralis minor and major, scaleni ) and conventional physiotherapy
    Intervention Type
    Other
    Intervention Name(s)
    Manual therapy and conventional physical therapy treatment
    Intervention Description
    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
    Primary Outcome Measure Information:
    Title
    chest expansion
    Description
    caliper will be used to assess chest expansion into centimeter
    Time Frame
    pre-intervention and after 8 weeks of intervention
    Title
    (the forced vital capacity (FVC), forced expiratory volume at first second (FEV1) and FEV1/FVC will be recorded. )
    Description
    spirometry used to measure
    Time Frame
    pre-intervention
    Title
    cranio-vertebral angle and kyphotic angle in degrees
    Description
    kinovea software will be used to assess in degrees
    Time Frame
    pre-intervention
    Title
    functional capacity.
    Description
    Six minute walk test will be used to assess functional capacity(meter/minutes)
    Time Frame
    pre-intervention
    Title
    dyspnea score
    Description
    Modified Borg scale will be used to assess dyspnea
    Time Frame
    pre-intervention

    10. Eligibility

    Sex
    Male
    Minimum Age & Unit of Time
    50 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    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
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Amira Saad Mohamed Morsy, Master
    Phone
    01092128481
    Email
    amira.saad.mm@gmail.com

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
    IPD Sharing Plan Description
    waiting to know the results of the intervention

    Learn more about this trial

    Selective Manual Therapy Techniques in Chronic Obstructive Pulmonary Disease

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