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Exercise Program Combined With Ergonomic Training in Textile Workers

Examining the Effectiveness of an Exercise Program Combined With Ergonomic Training for Textile Workers: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07408401
Enrollment
60
Registered
2026-02-13
Start date
2026-02-09
Completion date
2026-06-30
Last updated
2026-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Textile Worker

Keywords

breathing exercise, posture exercise, textile workers, ergonomics

Brief summary

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.

Interventions

OTHERSupervised Exercise

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

OTHERHome exercise

Home exercise with ergonomic and posture training

Sponsors

Okan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

Volunteers aged 18-60 who have been working in the textile industry for at least 6 months will be included in the study.

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Respiratory FunctionFrom enrollment to the end of treatment at 6 weeksA 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.
6-Minute Walk TestFrom enrollment to the end of treatment at 6 weeksThe 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.
Nordic Musculoskeletal System QuestionnaireFrom enrollment to the end of treatment at 6 weeksThe 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.

Secondary

MeasureTime frameDescription
New York Posture Rating ChartFrom enrollment to the end of treatment at 6 weeksThe 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."
Wall Push-Up TestFrom enrollment to the end of treatment at 6 weeksThe 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.
Sit-to-Stand TestFrom enrollment to the end of treatment at 6 weeksThe 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.
Fatigue Severity ScaleFrom enrollment to the end of treatment at 6 weeksThe 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.
Visual Analog ScaleFrom enrollment to the end of treatment at 6 weeksA simple assessment tool that allows individuals to express the intensity of a feeling, pain, or symptom visually rather than numerically. It typically uses a horizontal line 10 cm long; one end of the line represents the minimum, such as "none" or "mildest," while the other end represents the maximum, such as 'unbearable' or "most severe." The participant marks the degree of pain or symptoms they feel on this line, and the position of the mark is measured in millimeters or centimeters to obtain a numerical value. In this study, it will be assessed three times: at rest, while working, and for night pain.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026