NCT07360626 Exercise and Health Education for Textile Workers: A Pre-Post Study
| NCT ID | NCT07360626 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Universidad San Jorge |
| Condition | Musculoskeletal Disorders (MSDs) |
| Study Type | INTERVENTIONAL |
| Enrollment | 38 participants |
| Start Date | 2026-02-01 |
| Primary Completion | 2026-06-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 38 participants in total. It began in 2026-02-01 with a primary completion date of 2026-06-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Musculoskeletal disorders (MSDs) significantly impact quality of life, health status, and work ability. Standard treatments include ergonomic interventions, therapeutic exercise programs, education on risk prevention, active breaks, and physiotherapy. This study aims to assess the current physical and psychosocial condition of textile manufacturing workers and to evaluate the impact of a combine exercise and health education program on their physical and psychosocial outcomes. The eight-week intervention consists of a weekly in-person workshops and two asynchronous online exercise sessions per week via a mobile app, with exercises adjusted based on participant feedback. Participants will be recruited from voluntary textile workers at Lacor Textil, S.L., aged 18-65, with active employment. All participants will receive the intervention program. Primary objectives are to assess the baseline physical and psychosocial condition of participants and to evaluate the effects of the eight-week intervention on their physical fitness, musculoskeletal health, and overall psychosocial well-being Secondary objectives are to examine changes in the intensity and location of musculoskeletal pain and discomfort, the prevalence of symptoms in different body regions, upper and lower body strength using standardized tests, work ability and perception of work performance, and psychosocial and cognitive factors including sleep quality, stress, anxiety, depression, productivity, and quality of life. Hypothesis: The implementation of an eight-week physical exercise and health education program in textile workers will reduce perceived musculoskeletal discomfort and pain, and improve their physical fitness and psychosocial well-being.
Eligibility Criteria
Inclusion Criteria: * Have an active employment contract with Lacor Textil covering the entire duration of the study, including the month following the third evaluation phase. * Be aged 18-65 years (inclusive). * Be available to participate in all scheduled sessions. Exclusion Criteria: * Have severe or specific musculoskeletal conditions that contraindicate exercise. * Be currently pregnant. * Be receiving physiotherapy treatment concurrently. * Be on temporary sick leave during the intervention period. * Not have the physical capacity required to participate in the workshops and guided exercise. * Have cognitive or communication impairments that prevent adequate participation. * Complete less than 80% of the intervention program.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07360626 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 65 Years, studying Musculoskeletal Disorders (MSDs). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07360626 currently recruiting?
Yes, NCT07360626 is actively recruiting participants. Contact the research team at cjimenez@usj.es for enrollment information.
Where is the NCT07360626 trial being conducted?
This trial is being conducted at Zaragoza, Spain.
Who is sponsoring the NCT07360626 clinical trial?
NCT07360626 is sponsored by Universidad San Jorge. The trial plans to enroll 38 participants.