Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03871335
Other study ID # OrduU4
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 10, 2018
Est. completion date February 27, 2019

Study information

Verified date March 2019
Source T.C. ORDU ÜNIVERSITESI
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to determine the prevalence of work-related musculoskeletal disorders in female workers in hazelnut factory. The secondary aim is to investigate the relationship between the musculoskeletal disorders severity and working posture, work related factor, psychosocial factor.


Recruitment information / eligibility

Status Completed
Enrollment 114
Est. completion date February 27, 2019
Est. primary completion date February 15, 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- age >18 years,

- had at least 12 months of continuous working experience in hazelnut selection.

Exclusion Criteria:

- having pregnancy,

- working in a standing position or having a burden job,

- having joint disease, gout, diabetes, and trauma during the last one year

Study Design


Intervention

Diagnostic Test:
Investigation of the work-related musculoskeletal disorders
Structured questionnaires will be used to determine the prevalence of the work-related musculoskeletal disorders and work-related factor. Photogrammetric method will be used to evaluate working posture.

Locations

Country Name City State
Turkey Sevim ACARÖZ CANDAN Ordu Altinordu

Sponsors (3)

Lead Sponsor Collaborator
T.C. ORDU ÜNIVERSITESI Giresun University, Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Nordic Musculoskeletal Questionnaire (NMQ) NMQ will be used to determine the self-reported musculoskeletal symptoms in the different body part (neck, shoulder, elbow, wrist, upper back, lower back, hip, knee, ankle) in which suffered from aches, pain, or discomfort during the last 12 months. The states of the obtained sick leave from work, obstructing of work, taken medication and seen a doctor or physiotherapist etc. during the past 12 months regarding the work-related MSD will be questioned. The participants can be responded by "yes" or "no". 10 minutes
Secondary Dutch Musculoskeletal Questionnaire short version (DMQ-s) DMQ-s was used to evaluate the perceived workload, work-related risk factors, and general health status. DMQ-s involves four sections (general question, health, perceived workload, ergonomic environment). The score of the three sections except the general questions section will be summed. Higher scores means risky situation for work-related musculoskeletal disorders. 10 minutes
Secondary Assessment of the working posture The working posture will be assessed using the photogrammetry method which is a reliable and valid tool for postural angles analysis. The photographs were taken the lateral aspect of the workers using a digital, professional camera (Canon 4000D, Japan) from a 150cm distance, at the height of the acromion in working position. Cranio-vertebral angle (CVA), thoracic kyphosis and lumbar lordosis angles were measured on the photograph using the ImageJ program. The results will be recorded as degree. 2 minutes
Secondary Rapid Upper Extremity Assessment Rapid Upper Limb Assessment (RULA) is a tool to evaluate upper extremity MSD risk factors. The RULA ergonomic assessment tool considers biomechanical and postural load requirements of job tasks/demands on the neck, trunk and upper extremities. A single page worksheet is used to evaluate required body posture, force, and repetition. Based on the evaluations, scores are entered for each body region in section A for the arm and wrist, and section B for the neck and trunk. After the data for each region is collected and scored, tables on the form are then used to compile the risk factor variables, generating a single score that represents the level of MSD risk. The score means 1-2 negligible risk no change requirement, 3-4 low risk change may be needed requirement, 5-6 medium risk further investigation change soon, 6+ very high risk implement change now 5 minutes
Secondary Short Form-12 Health Survey (SF-12 Health Survey) SF-12 Health Survey is a multidimensional generic measure of health-related quality of life. SF-12 Health Survey includes two subdomains as physical and mental. SF-12 Health Survey has a scoring algorithm. The higher scores defines good quality of life. 5 minutes
Secondary Pain Severity Pain severity will be scored between 0 and 10. The pain of nine different body part (neck, shoulder, elbow, wrist, upper back, lower back, hip, knee, ankle) will be examined by the subject's perception. 5 minutes
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05559255 - Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI N/A
Terminated NCT04356352 - Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain Phase 2/Phase 3
Completed NCT04748367 - Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care N/A
Completed NCT05057988 - Virtual Empowered Relief for Chronic Pain N/A
Completed NCT04466111 - Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
Recruiting NCT05868122 - A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy Phase 3
Recruiting NCT06206252 - Can Medical Cannabis Affect Opioid Use?
Active, not recruiting NCT05006976 - A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study N/A
Completed NCT03273114 - Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain N/A
Enrolling by invitation NCT06087432 - Is PNF Application Effective on Temporomandibular Dysfunction N/A
Completed NCT05508594 - Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001 Phase 2/Phase 3
Recruiting NCT03646955 - Partial Breast Versus no Irradiation for Women With Early Breast Cancer N/A
Active, not recruiting NCT03472300 - Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
Completed NCT03678168 - A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries N/A
Completed NCT03931772 - Online Automated Self-Hypnosis Program N/A
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Completed NCT02913027 - Can We Improve the Comfort of Pelvic Exams? N/A
Terminated NCT02181387 - Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor? Phase 4
Recruiting NCT06032559 - Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment Phase 3
Active, not recruiting NCT03613155 - Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care