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Not yet recruiting NCT07548216

Efficacy of Osteopathic Manipulative Techniques With Progressive Pulmonary Fibrosis Patients

No phase Interventional Osteopathic Manipulative Treatment

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: osteopathic manipulative techniques, conventional chest physiotherapy.
Who it may be relevant to
Registry conditions: Osteopathic Manipulative Treatment. Basic parameters: 19 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Efficacy of Selected Osteopathic Manipulative Techniques as a Conjunctive Therapy for Patients With Progressive Pulmonary Fibrosis

Overview

The goal of this clinical trial is to learn if osteopathic manipulative techniques add benefits for treatment of patients with progressive pulmonary fibrosis. The main questions it aims to answer are : Could osteopathic manipulative techniques add benefits for treatment of patients with progressive pulmonary fibrosis? Researchers will compare osteopathic manipulative techniques with chest physiotherapy to chest physiotherapy alone to see if osteopathic manipulative techniques works to treat progressive pulmonary fibrosis. Participants will: Take osteopathic manipulative techniques 2 days a week for 4 weeks and chest physiotherapy 3 days a week for 4 weeks

Detailed description

In this study researchers want to see if osteopathic manipulative techniques add benefits to treat progressive pulmonary fibrosis.

two group of patients : study group will receive osteopathic manipulative techniques with conventional chest physiotherapy .

control group will receive only conventional chest physiotherapy . osteopathic manipulative techniques will be done for 2 days a week for 4 weeks while conventional chest physiotherapy will be done 3 days a week for 4 weeks.

Interventions

  • Other osteopathic manipulative techniques
    for 4 weeks , 2 sessions per week
  • Other conventional chest physiotherapy
    for 4 weeks , 3 sessions per week

Primary outcome measures

  • pulmonary function test - FVC [Time frame: preintervention , post intervention after 4 weeks]
  • pulmonary function test - FEV [Time frame: pre intervention , post intervention after 4 weeks]
  • pulmonary function test - FEV/FVC [Time frame: pre intervention , post intervention after 4 weeks]
Secondary outcome measures (2)
  • chest expansion measurment [Time frame: pre intervention , post intervention after 4 weeks]
  • Modified Medical Research Council dyspnea scale [Time frame: pre intervention , post intervention after 4 weeks]

Eligibility criteria

Inclusion criteria

  • Their age > 18.
  • Both sexes.
  • Patients without excerbations.
  • FVC of the patient <50% .
  • FEV1/ FVC of the patient <50%.
  • Hemodynamic stable.
  • Conscious and cooperative.
  • Are able to participate in training actively.

Exclusion criteria

  • Patients with acute excerbations.
  • Acute or Uncontrolled Infections.
  • Active Malignancy.
  • Chest deformity

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Egypt · 1 center
  • Hospital of Beni Suef University — Banī Suwayf

Identifiers

NCT: NCT07548216 · FPTBSUREC/0405/2325

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗