Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06297798
Other study ID # SakaryaAppliedSciencesUPNS
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 14, 2024
Est. completion date May 10, 2024

Study information

Verified date March 2024
Source Sakarya Applied Sciences University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date May 10, 2024
Est. primary completion date March 21, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 30 Years to 65 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Turkey Sakarya University of Applied Sciences Sakarya

Sponsors (1)

Lead Sponsor Collaborator
Sakarya Applied Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary MUSCLE SKELETAL SYSTEM ASSESSMENT 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 Posture Measures 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
See also
  Status Clinical Trial Phase
Withdrawn NCT04976972 - A Comparison of Patients Receiving a Total Knee Replacement With Robotic Assistance or With Conventional Instrumentation N/A
Recruiting NCT05546541 - Epidemiology and Nutrition
Completed NCT05071469 - Comparison of Two Different Treatment Methods N/A
Completed NCT05041400 - Distribution of Knee Isokinetic Angle-specific Moments and Ratios N/A
Not yet recruiting NCT06216028 - Bone Marrow Aspirate Concentrate (BMAC) Treatment for Knee Osteoarthritis Phase 3
Not yet recruiting NCT04932993 - Writing Down Goals N/A
Completed NCT02944448 - A Study Evaluating Pain Relief and Safety of Orally Administered CR845 in Patients With Osteoarthritis of Hip or Knee Phase 2
Completed NCT02256098 - RSA RCT: ATTUNEā„¢ TKA Versus PFC Sigma TKA N/A
Completed NCT02269254 - Persona Versus NexGen N/A
Completed NCT02257489 - Phase 1 Study of ACE-083 in Healthy Subjects Phase 1
Completed NCT01979731 - Effects Job Rotation in the Prevention of Work Related Musculoskeletal Disorders N/A
Active, not recruiting NCT01440153 - Additional Exercise Program in Professional Dancers N/A
Completed NCT00968266 - Improving Beliefs About Medication in Patients With Rheumatoid Arthritis N/A
Completed NCT05222126 - Efficacy of Ultrasound-Guided Hydrodissection in Carpal Tunnel Syndrome N/A
Completed NCT05062694 - Physical Therapy Management Of The Patient With Central Sensitization
Recruiting NCT05564182 - High Intensity Laser Therapy in the Treatment of Hemiplegic Shoulder Pain N/A
Completed NCT04009369 - Impacts of Physiotherapy Services in a Quebec Emergency Department N/A
Completed NCT05561452 - The Efficacy of PRP Injection in the Treatment of Rotator Cuff Syndrome N/A
Recruiting NCT05432609 - Standardization and Reproducibility Regarding Scanning Procedures and Measurements of Weight-bearing Cone Beam CT in the Lower Extremity
Completed NCT04959162 - The Effect of Theoretical Knowledge on Resident's Practical Performance in Musculoskeletal Ultrasound N/A