Exercise Program Combined With Ergonomic Training in Textile Workers

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorOkan University

About this trial

Most studies in the literature focus on musculoskeletal disorders and pain levels in occupational groups with repetitive workloads, such as textile workers. However, due to the nature of the work environment, decreased respiratory function and postural disorders are also frequently observed in these individuals. There is no comprehensive study in the literature that combines respiratory exercises, posture training, and ergonomics training for textile workers. Therefore, this study will examine the effects of a regular exercise program implemented alongside ergonomics training provided to textile workers on respiratory parameters, musculoskeletal disorders, posture, functionality, pain levels, and fatigue intensity.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

Individuals with orthopedic or neurological conditions that prevent exercise,

those with chronic pulmonary disease, those with psychological disorders, and

those who have undergone surgery that prevents exercise will not be included in the study.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Supervised Exercise

    Other intervention

    Supervised exercise (breathing and chair-based exercise) with ergonomic and posture training

  • Home exercise

    Other intervention

    Home exercise with ergonomic and posture training

Treatment groups

60 Participants
are divided into 3 treatment groups
Group A: Home exercise groupActive comparator 1 intervention
Group B: Supervised groupExperimental treatment 1 intervention
Group C: Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Respiratory Function

A spirometer is an objective device used to measure lung air volumes and flow rates. This test is performed by the individual taking a deep breath and then blowing out forcefully, yielding various parameters. Spirometry results help identify obstructive (e.g., COPD, asthma) or restrictive (e.g., fibrosis) types of respiratory dysfunction. It is frequently used in clinical and occupational health settings, particularly to monitor respiratory function in individuals working in dusty environments such as textiles.

Time frame
From enrollment to the end of treatment at 6 weeks
2

Respiratory Function

Chest circumference measurement: Chest circumference measurement is a simple, non-invasive method used to assess the effectiveness of the respiratory muscles and the mobility of the rib cage. In this measurement, a tape measure is used to determine the amount of change in chest circumference during inspiration (breathing in) and expiration.

Time frame
From enrollment to the end of treatment at 6 weeks
3

6-Minute Walk Test

The 6-Minute Walk Test is a practical and reliable field test used to assess an individual's submaximal aerobic capacity and functional exercise level. In the test, the participant walks as fast as possible, but at a safe pace, for 6 minutes on a flat corridor. The total distance covered during the test will be recorded in meters.

Time frame
From enrollment to the end of treatment at 6 weeks
4

Nordic Musculoskeletal System Questionnaire

The Nordic Musculoskeletal System Questionnaire (NMQ) is a standardized self-report questionnaire developed to identify musculoskeletal disorders experienced by individuals in different body regions. It asks about pain, discomfort, or loss of function experienced in nine different body regions-neck, shoulder, back, waist, hip, knee, and wrist-over the past 12 months and the past 7 days. The questionnaire is widely used in the assessment of ergonomic risks and work-related musculoskeletal disorders. It is simple, quick to administer, and suitable for comparative analysis in large populations.

Time frame
From enrollment to the end of treatment at 6 weeks

Secondary outcomes

1

New York Posture Rating Chart

The New York Posture Analysis is an observational assessment method used to systematically and objectively evaluate an individual's body posture. In this analysis, specific segments of the body such as the head, shoulders, torso, hips, knees, and ankles are observed from the front, side, and back, and 13 different posture regions are scored. Each region is scored between 1 and 5; high scores indicate better postural alignment, while low scores indicate postural abnormalities. Based on the total score, the individual's overall posture is classified as "good," "moderate," or "poor."

Time frame
From enrollment to the end of treatment at 6 weeks
2

Wall Push-Up Test

The wall push-up test is a simple physical performance test used to assess upper extremity muscle strength and endurance. The participant places their hands shoulder-width apart on the wall and performs push-ups by flexing and extending their elbows while keeping their body in a straight line. The time taken to complete 5 repetitions will be recorded. The test is frequently used to measure the strength of the shoulder, arm, and chest muscles, as well as to assess upper body endurance.

Time frame
From enrollment to the end of treatment at 6 weeks
3

Sit-to-Stand Test

The Sit-to-Stand Test is a performance test that evaluates lower extremity muscle strength, balance, and functional mobility. The participant sits down and stands up from a chair of standard height as many times as possible within 30 seconds, and the total number of repetitions will be measured. The test objectively determines lower extremity function and muscle endurance, which play an important role in daily living activities.

Time frame
From enrollment to the end of treatment at 6 weeks
4

Fatigue Severity Scale

The Fatigue Severity Scale is a valid and reliable self-report measure developed to subjectively assess the level of fatigue that affects individuals' daily lives. This scale consists of a total of 9 items and uses a Likert-type rating system where each item is scored on a scale from 1 (strongly disagree) to 7 (strongly agree). Fatigue severity is determined by taking the average of the participant's total score; an increase in the average score indicates an increase in fatigue level.

Time frame
From enrollment to the end of treatment at 6 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: