- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06268548
Effect of Manual Diaphragmatic Activation on Diaphragm Function in Patients With Gastroesophageal Reflux Disease
February 12, 2024 updated by: Shimaa Goda Sherif Ali, Cairo University
This study was conducted to investigate Effect of manual diaphragmatic activation on diaphragm function in patients with gastroesophageal reflux disease
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Thirty both gender patients with gastroesophageal reflux disease enrolled in this study , study group And control group.
To investigate Effect of manual diaphragmatic activation on diaphragm function in patients with gastroesophageal reflux disease
Study Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Shimaa Goda Sherif, Master
- Phone Number: 01008804063
- Email: shimaaagoda@gmail.com
Study Locations
-
-
-
Giza, Egypt, 12613
- Recruiting
- Faculty of Physical Therapy
-
Contact:
- Nesreen Ghareb Mohamed, Professor
- Phone Number: 01002227242
- Email: nesreen.elnahas@pt.cu.edu.eg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- patients with gastroesophageal reflux disease.
- the age will be ranged from 20 to 50 .
- body mass index from 20 to 34,9 kg/m2 .
- low level of physical therapy
Exclusion Criteria:
- Pregnancy
- open wound
- abdominal or spinal surgery
- Congenital or acquired disorder
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Study
Experimental , diaphragmatic activation with medical treatment ,15patients with gastroesophageal reflux disease do manual diaphragmatic activation in additional to traditional medical treatment
|
Manual diaphragm release on diaphragm
|
|
No Intervention: Control
30 patients with gastroesophageal reflux disease taking traditional medical treatment only
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diaphragm Excursion
Time Frame: 2 months
|
Diaphragm Excursion
|
2 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 15, 2023
Primary Completion (Estimated)
February 20, 2024
Study Completion (Estimated)
February 27, 2024
Study Registration Dates
First Submitted
February 4, 2024
First Submitted That Met QC Criteria
February 12, 2024
First Posted (Actual)
February 20, 2024
Study Record Updates
Last Update Posted (Actual)
February 20, 2024
Last Update Submitted That Met QC Criteria
February 12, 2024
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004790
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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