- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06070584
Effect of Respiratory Muscle Training on Lung Function on Quarry Workers in Minia Government Egypt
November 5, 2023 updated by: Deraya University
forty quarry workers participated in the study with age range (40-60 years), body mass index (BMI) from 25 to 34.9 kg/m2 (over weight and class 1 obesity).
The patients divided into two groups randomly.
(Group A) received aerobic exercises (Group B) receive aerobic exercises with moderate intensity in the form of walking on electrical treadmill for 30 min and inspiratory muscle training for 10 minutes., 3 sessions per week for 8 consecutive weeks.
Pulmonary function test was applied by spirometry to assess lung function
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Minya, Egypt, 05673
- Soad A. Mohamad
-
-
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:
- quarry workers working in the quarries for five years ago at least saver from chest diseases\\
- BMI ranged from 25 to 34.9 kg/cm2
Exclusion Criteria:
- Subject with infected chest disease, unstable mental condition and chest cancer patients
- musculoskeletal disease
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: group A
received aerobic exercises only
|
aerobic exercises with moderate intensity in the form of walking on electrical treadmill
|
Experimental: Group B
aerobic exercises with moderate intensity in the form of walking on electrical treadmill
|
aerobic exercises with moderate intensity in the form of walking on electrical treadmill
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
adequate lung function
Time Frame: 8 weeks
|
Spirometer test, The patient was instructed to take a big breath in and then exhale as forcefully and quickly as they could, continuing until there was no more air remaining, in order to measure FVC and FEV1
|
8 weeks
|
patient satisfaction
Time Frame: 8 weeks
|
VAS scoring, (no pain=0) and the other end (worst pain=10).
|
8 weeks
|
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)
January 2, 2023
Primary Completion (Actual)
May 2, 2023
Study Completion (Actual)
October 2, 2023
Study Registration Dates
First Submitted
September 24, 2023
First Submitted That Met QC Criteria
September 30, 2023
First Posted (Actual)
October 6, 2023
Study Record Updates
Last Update Posted (Actual)
November 7, 2023
Last Update Submitted That Met QC Criteria
November 5, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 4/23
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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