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Effect of Aerobic and Resistance Exercise on Quarry Workers

NCT07744334 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75

Last updated 2026-08-05

No results posted yet for this study

Summary

The goal of this randomized clinical trial is to compare the effects of aerobic exercise training and resistance exercise training on ventilatory function in quarry workers. It will also evaluate their effects on functional capacity and health-related quality of life (HRQOL).

The main questions it aims to answer are:

Does aerobic exercise training improve ventilatory function more effectively than resistance exercise training? How do aerobic and resistance exercise training affect functional capacity and health-related quality of life in quarry workers?

Researchers will compare aerobic exercise training and resistance exercise training with a control group receiving routine treatment and breathing exercises to determine which intervention is more effective in improving ventilatory function, functional capacity, and health-related quality of life.

Participants will:

Be randomly assigned to one of three groups: an aerobic exercise training group, a resistance exercise training group, or a control group.

Receive the assigned intervention three times per week for eight consecutive weeks.

Undergo ventilatory function assessment using spirometry. Complete assessments of functional capacity and health-related quality of life before and after the intervention.

Conditions

Interventions

PROCEDURE

Aerobic exercise training

participants will receive aerobic exercise training in addition to routine medical treatment and breathing exercise training.

PROCEDURE

Resistance exercise training

participants will receive resistance exercise training in addition to routine medical treatment and breathing exercise training.

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Principal Investigators

  • Elsayed E Felaya, Assoiate Professor · Cairo University

  • Shimaa T Taha, Lecturer · Cairo University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
40 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-09
Primary Completion
2026-10-24
Completion
2027-01-25

Countries

  • Egypt

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07744334 on ClinicalTrials.gov