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NCT06070584 Clinical Trial

Effect of Respiratory Muscle Training on Lung Function on Quarry Workers in Minia Government Egypt

Lung Function Decreased Clinical Trial

Official title:
Effect of Respiratory Muscle Training on Lung Function on Quarry Workers in Minia Government Egypt

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06070584
Other study ID # 4/23
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date January 2, 2023
Est. completion date October 2, 2023

Study information
Verified date November 2023
Source Deraya University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date October 2, 2023
Est. primary completion date May 2, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 40 Years to 60 Years
Eligibility 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 Design

Related Conditions & MeSH terms

Intervention

Procedure:
• aerobic exercises with electrical treadmill for 30 min and inspiratory muscle training for 10 minutes.,
aerobic exercises with moderate intensity in the form of walking on electrical treadmill

Locations
Country Name City State
Egypt Soad A. Mohamad Minya

Sponsors (1)
Lead Sponsor Collaborator
Deraya University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary adequate lung function 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
Primary patient satisfaction VAS scoring, (no pain=0) and the other end (worst pain=10). 8 weeks
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