The Effect of Online Rehabilitation Applications on Pain and Quality of Life in Textile Workshop Workers

July 19, 2024 updated by: AYCAN ÇAKMAK REYHAN, Istanbul Bilgi University

Musculoskeletal problems are a common health issue among individuals working in textile workshops, attributed to factors such as ergonomic risks in working conditions, personal characteristics of employees, and other workplace factors. Neck pain, back pain, shoulder pain, wrist pain, hand and finger pain, knee pain, and foot pain are frequently observed issues among those working in textile workshops, negatively impacting their functionality and quality of life.

The research aims to investigate the effects of online rehabilitation education on pain and quality of life among textile workers. Participants aged between 21 and 52 working in textile workshops will be included in the study. All participants will be evaluated twice, before and after treatment, with all assessments conducted face-to-face. Demographic information such as age, gender, marital status, etc., will be assessed using a structured socio-demographic form. Pain levels will be assessed using the 100 mm VAS, quality of life will be assessed using the SF-36 questionnaire, and posture evaluation will be conducted using anterior and lateral posture analysis. The rehabilitation program administered to participants will take place over a period of 3 months, with sessions conducted three times a week on an online platform. The rehabilitation program will include posture exercises, stretching exercises, exercises for normal joint range of motion, strengthening exercises, regional pain education (shoulder, elbow, hip, wrist), and discussions on good and poor posture, lasting approximately 40-45 minutes.

Study Overview

Detailed Description

Musculoskeletal system problems are a common health issue among individuals working in textile workshops. The causes of these problems include ergonomic risks in working conditions, personal characteristics of employees, and other workplace factors. Ergonomic risks are the most significant cause of musculoskeletal system problems in textile workshops. These risks can stem from factors such as the working positions of employees, equipment used, and the nature of the work itself. For example, factors like prolonged static postures, lifting and carrying heavy objects, performing repetitive movements, and using poorly designed equipment can contribute to musculoskeletal system problems. Personal characteristics of employees can also increase the risk of musculoskeletal system problems. For instance, employees who start working at a young age, are overweight, have poor posture habits, or smoke are more susceptible to these problems. Other workplace factors can also contribute to musculoskeletal system problems. Factors like poor ventilation, noise, and lighting can adversely affect the musculoskeletal system of employees. These problems typically manifest with symptoms such as pain, loss of strength, numbness, tingling, and swelling. In some cases, they can lead to more serious issues such as muscle tears and osteoarthritis. Common problems among individuals working in textile workshops include neck pain, back pain, shoulder pain, wrist pain, hand and finger pain, knee pain, and foot pain. These problems negatively impact the functionality and quality of life of individuals working in textile workshops.

The aim of the research is to examine the impact of an online rehabilitation program applied to individuals working in textile workshops on pain and quality of life. The desired outcome of the research is for the online rehabilitation program applied to individuals working in textile workshops to reduce pain symptoms and increase their quality of life.

Study Type

Interventional

Enrollment (Actual)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • Istanbul Bilgi University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • To be between the ages of 21 and 52. To have worked in the textile sector for at least 2 years. To be a smartphone user.

Exclusion Criteria:

  • Having a surgical history in the past six months. Having a history of cardiovascular disease that would hinder exercise. Having mental disorders. Having received physical therapy in the past six months.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: exercise
Participants in the research will undergo a three-week online rehabilitation program, three times a week, lasting 40-45 minutes each session. The program includes posture, stretching, joint range of motion, strengthening exercises, pain education, and discussions. Conducted via Zoom, only the practitioner will be present during sessions. Non-attendance for two consecutive sessions or failure to provide feedback will result in exclusion. Exercises cover various body areas and types, including posture correction, range of motion, stretching, isometric neck and shoulder exercises, stick exercises, and strengthening exercises.
Participants in the research will undergo a three-week online rehabilitation program, three times a week, lasting 40-45 minutes each session. The program includes posture, stretching, joint range of motion, strengthening exercises, pain education, and discussions. Conducted via Zoom, only the practitioner will be present during sessions. Non-attendance for two consecutive sessions or failure to provide feedback will result in exclusion. Exercises cover various body areas and types, including posture correction, range of motion, stretching, isometric neck and shoulder exercises, stick exercises, and strengthening exercises.
Experimental: plasebo
They won't exercise. They will only be evaluated at the beginning and after 2 months.
Participants in the research will undergo a three-week online rehabilitation program, three times a week, lasting 40-45 minutes each session. The program includes posture, stretching, joint range of motion, strengthening exercises, pain education, and discussions. Conducted via Zoom, only the practitioner will be present during sessions. Non-attendance for two consecutive sessions or failure to provide feedback will result in exclusion. Exercises cover various body areas and types, including posture correction, range of motion, stretching, isometric neck and shoulder exercises, stick exercises, and strengthening exercises.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
VAS scale for pain assessment
Time Frame: baseline and 8 weeks assessment
Participants' pain will be assessed using the 100 mm Visual Analog Scale (VAS) in the research conducted with individuals working in textile workshops. The participants' pain will be evaluated at three time intervals: at rest, while working in the textile workshop, and at night. Participants will be asked to mark their perceived pain intensity on a straight line of 0 mm (no pain at all) to 100 mm (unbearable pain). The intensity of the perceived pain will be measured and recorded in millimeters (mm) at the end of the assessment.
baseline and 8 weeks assessment

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Posture assessment
Time Frame: Baseline and 8 weeks assessment
The posture of individuals employed in the textile workshop included in the study will be evaluated through anterior and lateral posture analysis.
Baseline and 8 weeks assessment
SF36 scale for quality of life assessment
Time Frame: Baseline and 8 weeks assessment
The quality of life of individuals employed in the textile workshop included in the study will be evaluated using the Short Form-36 (SF-36) scale. The scale includes questions related to physical functioning, social functioning, role limitations due to physical problems, role limitations due to emotional problems, mental health, energy, pain, and general perception of health. Textile workers will choose the response option that best suits them from the questionnaire. The scale is scored between "0" and "100". A score of "0" indicates poor health status, while a score of "100" indicates no health problems.
Baseline and 8 weeks assessment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 7, 2024

Primary Completion (Actual)

June 25, 2024

Study Completion (Actual)

June 30, 2024

Study Registration Dates

First Submitted

April 17, 2024

First Submitted That Met QC Criteria

April 30, 2024

First Posted (Actual)

May 1, 2024

Study Record Updates

Last Update Posted (Actual)

July 22, 2024

Last Update Submitted That Met QC Criteria

July 19, 2024

Last Verified

July 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • IstanbulBuuu

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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