NCT07408401

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
2mo left

Started Feb 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress62%
Feb 2026Jun 2026

First Submitted

Initial submission to the registry

January 23, 2026

Completed
17 days until next milestone

Study Start

First participant enrolled

February 9, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

February 13, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 15, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

February 13, 2026

Status Verified

February 1, 2026

Enrollment Period

3 months

First QC Date

January 23, 2026

Last Update Submit

February 10, 2026

Conditions

Keywords

breathing exerciseposture exercisetextile workersergonomics

Outcome Measures

Primary Outcomes (4)

  • 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.

    From enrollment to the end of treatment at 6 weeks

  • 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.

    From enrollment to the end of treatment at 6 weeks

  • 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.

    From enrollment to the end of treatment at 6 weeks

  • 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.

    From enrollment to the end of treatment at 6 weeks

Secondary Outcomes (5)

  • New York Posture Rating Chart

    From enrollment to the end of treatment at 6 weeks

  • Wall Push-Up Test

    From enrollment to the end of treatment at 6 weeks

  • Sit-to-Stand Test

    From enrollment to the end of treatment at 6 weeks

  • Fatigue Severity Scale

    From enrollment to the end of treatment at 6 weeks

  • Visual Analog Scale

    From enrollment to the end of treatment at 6 weeks

Study Arms (3)

Home exercise group

ACTIVE COMPARATOR

This group will receive a brochure containing an exercise program they can do at home, along with training on ergonomics and posture.

Other: Home exercise

Supervised group

EXPERIMENTAL

In this group, ergonomics and posture training will be taught in person, and exercise applications will be carried out in the form of supervised group exercises.

Other: Supervised Exercise

Control Group

NO INTERVENTION

In this group, no applications will be made; only assessments will be conducted at the beginning and end of the work.

Interventions

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

Supervised group

Home exercise with ergonomic and posture training

Home exercise group

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

January 23, 2026

First Posted

February 13, 2026

Study Start

February 9, 2026

Primary Completion (Estimated)

May 15, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

February 13, 2026

Record last verified: 2026-02