Effects of Telerehabilitation-Based Interventions on the Musculoskeletal System in Drivers

March 13, 2024 updated by: Pakize Nurgul Sen, Sakarya Applied Sciences University

Effects of Telerehabilitation-Based Interventions on the Musculoskeletal System in Drivers: A Crossover Longitudinal Study

This study is designed to examine the effect of telerehabilitation application on the musculoskeletal system of drivers.The study will include 40 voluntary participants who work as drivers on inter-district routes in Sakarya. The participants' sociodemographic information, musculoskeletal problems, and postures will be assessed. Participants will be divided into two groups: one group will receive tele-rehabilitation with posture and stabilization exercises, while the other group will serve as the control group. The exercises will be implemented for 10 weeks, followed by an 8-week tapering period, after which the groups will be crossed over. A re-evaluation will be conducted after 10 weeks, with follow-up assessments scheduled for 3 months later.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Detailed Description

The aim of the research is to investigate the effectiveness of telerehabilitation-based interventions in the management and improvement of common musculoskeletal disorders prevalent among drivers. This study will longitudinally examine the potential effects of developing and implementing customized posture and stabilization exercise programs for reducing posture and musculoskeletal disorders in drivers. The goal is to provide evidence of the effectiveness of telerehabilitation applications on the musculoskeletal health of drivers.

The study plans to involve 40 male volunteers aged 30-65 engaged in inter-district driving in Sakarya. Inclusion criteria for the study include working as an inter-district driver, driving a vehicle for at least 6 hours per day for a minimum of one year, and the ability to use at least one of the WhatsApp, Zoom, or Teams applications. Exclusion criteria include undergoing orthopedic surgery in the past year and a lack of consent to participate in the study. Within the scope of the study, sociodemographic information will be collected from all participants, their postures will be assessed using the "posture screen" application, and musculoskeletal problems will be evaluated using the "Cornell Musculoskeletal Disorders Questionnaire."

At the end of the assessment, participants will be divided into two groups using the layered randomization method. The intervention group will receive posture and stabilization exercises through telerehabilitation via WhatsApp, Zoom, or Teams applications for 45 minutes per day, five days a week, for 10 weeks. General advice will be given to both groups, but no exercise program will be provided to the control group. After 10 weeks, the same assessments will be conducted for both the control and intervention groups. Subsequently, an 8-week tapering period will be expected, followed by the crossover of the groups. Those initially in the intervention group will form the control group, and vice versa.

After 10 weeks of training, the same assessments will be conducted again, and following this assessment, a final evaluation will be conducted 3 months later to complete the follow-up.

Study Type

Interventional

Enrollment (Estimated)

40

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

      • Sakarya, Turkey, 54000
        • Sakarya University of Applied Sciences
        • Contact:
        • Principal Investigator:
          • Ceyhun TURKMEN, Assoc. Prof.

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Individuals working as drivers in intercity minibuses in Sakarya.
  • Those who have been working as drivers for at least one year.
  • Age between 30 and 65.
  • Male gender.
  • Those who can use a smartphone.
  • Those who can use at least one of the following applications: WhatsApp, Zoom, or Teams.

Exclusion Criteria:

  • Orthopedic surgeries undergone within the past year.
  • Inability to obtain consent to participate in the study.

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: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Telerehabilitation Group

In the telerehabilitation group, posture and stabilization exercises will be performed using Whatsapp and Zoom applications for 40 minutes, 5 days a week. Exercises will be applied for 10 weeks.

Posture and Stabilization Exercise Program:

  1. Stretching of neck flexor, extensor, and lateral flexor muscles (30 seconds each)
  2. Pectoral muscle stretching (30 seconds, 3 repetitions)
  3. Isometric neck exercises (10 seconds, 10 repetitions)
  4. Rhomboid strengthening exercise (bringing shoulder blades closer together against resistance using a TheraBand) (10 seconds, 10 repetitions)
  5. Stretching of hamstring, lumbar lordosis and gastrocnemius muscles (sitting and standing) (30 seconds, 3 repetitions)
  6. Pelvic posterior tilt exercise (10 seconds, 10 repetitions)
  7. Bridge exercise (20 seconds, 10 repetitions)
  8. Single-leg bridge exercise (Right-Left) (10 seconds, 10 repetitions)
  9. Plank (starting with 60 seconds, increasing by 10 seconds each week)

The telerehabilitation program will be implemented using Whatsapp and Zoom applications for 40 minutes, 5 days a week. Posture and stabilization exercises will be performed, and the exercises will be performed for 10 weeks.

Posture and Stabilization Exercise Program:

  1. Stretching of neck flexor, extensor, and lateral flexor muscles (30 seconds each)
  2. Pectoral muscle stretching (30 seconds, 3 repetitions)
  3. Isometric neck exercises (10 seconds, 10 repetitions)
  4. Rhomboid strengthening exercise (bringing shoulder blades closer together against resistance using a TheraBand) (10 seconds, 10 repetitions)
  5. Stretching of hamstring, lumbar lordosis and gastrocnemius muscles (sitting and standing) (30 seconds, 3 repetitions)
  6. Pelvic posterior tilt exercise (10 seconds, 10 repetitions)
  7. Bridge exercise (20 seconds, 10 repetitions)
  8. Single-leg bridge exercise (Right-Left) (10 seconds, 10 repetitions)
  9. Plank (starting with 60 seconds, increasing by 10 seconds each week)
No Intervention: Control Group
The control group will not be given any exercise program; instead, general posture recommendations will be given.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MUSCLE SKELETAL SYSTEM ASSESSMENT
Time Frame: Through study completion, an average of 1 year
The Cornell Musculoskeletal System Questionnaire will be used for musculoskeletal system evaluation. While conducting the survey, the illnesses experienced by the employees in the last week are taken as basis. In this survey, neck, shoulder (right-left), back, upper arm (right-left), waist, forearm (right-left), wrist (right-left), hip, upper leg (right-left), knee. Questions are asked for 20 body parts such as (right-left), lower leg (right-left) and foot (right-left) and the risk score is calculated as a result of the answers received. While calculating the relevant score, risk scores are calculated separately for each body region by multiplying scores such as the number of times the employee has experienced the discomfort in the current area, the severity of the discomfort felt and the obstacle in working. The final total score is calculated. A high score indicates high discomfort.
Through study completion, an average of 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Posture Measures
Time Frame: Through study completion, an average of 1 year
Posture evaluation will be made using the "PostureScreen Mobile" application. This application is a reliable and valid mobile tool designed specifically to assess static posture and, in particular, forward head tilt. All participants will be allowed to wear thin, tight clothing provided that reference anatomical landmarks are clearly visible. All evaluations will be repeated in the same place and under the same conditions. The photo will always be taken from a distance of 10 feet (approximately 3.5 meters) and from a height of 3.5 feet (approximately 1.5 meters).
Through study completion, an average of 1 year

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 (Estimated)

March 14, 2024

Primary Completion (Estimated)

March 21, 2024

Study Completion (Estimated)

May 10, 2024

Study Registration Dates

First Submitted

March 1, 2024

First Submitted That Met QC Criteria

March 1, 2024

First Posted (Actual)

March 7, 2024

Study Record Updates

Last Update Posted (Actual)

March 15, 2024

Last Update Submitted That Met QC Criteria

March 13, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • SakaryaAppliedSciencesUPNS

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.

Clinical Trials on Musculoskeletal Diseases

Clinical Trials on Telerehabilitation

3
Subscribe