Investigation of the Effects of Upper Extremity Functions in Female Patients With Non-Specific Neck Pain

January 22, 2024 updated by: Abdulkadir GOZ, Dokuz Eylul University

Investigation of the Effects of Upper Extremity Functions and Health-Related Quality of Life in Female Patients With Non-Specific Neck Pain

Non-specific neck pain is defined as pain in the posterior and lateral part of the neck between the superior nuchael line and the spinous process of the 1st thoracic vertebra, without neurological findings and obvious structural pathology. It is more common in women than in men. Neck pain is thought to affect upper extremity functions. Although the exact cause is unknown, it has been reported that mechanical loading, minor peripheral nerve damage and deconditioning negatively affect upper extremity functions in individuals with neck pain and reduce the quality of life. Although it is stated in the literature that patients with neck pain often experience upper extremity problems, there are a limited number of studies evaluating the relationship between the neck and upper extremity.

This study was planned to determine upper extremity functions and their impact on health-related quality of life in female patients with NSHP. Female patients with NSHP over the age of 18 who apply to Tarsus State Hospital Physical Therapy and Rehabilitation Clinic, meet the inclusion criteria, and agree to participate in the study will be included in the study. With our research, patients' upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life will be evaluated and interpreted.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Non-specific neck pain is defined as pain in the posterior and lateral part of the neck between the superior nuchael line and the spinous process of the 1st thoracic vertebra, without neurological findings and obvious structural pathology. It is more common in women than in men. Neck pain is thought to affect upper extremity functions. Although the exact cause is unknown, it has been reported that mechanical loading, minor peripheral nerve damage and deconditioning negatively affect upper extremity functions in individuals with neck pain and reduce the quality of life. Although it is stated in the literature that patients with neck pain often experience upper extremity problems, there are a limited number of studies evaluating the relationship between the neck and upper extremity.

This study was planned to determine upper extremity functions and their impact on health-related quality of life in female patients with NSHP. Female patients with NSHP over the age of 18 who apply to Tarsus State Hospital Physical Therapy and Rehabilitation Clinic, meet the inclusion criteria, and agree to participate in the study will be included in the study. With our research, patients' upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life will be evaluated and interpreted.

Study Type

Observational

Enrollment (Estimated)

80

Contacts and Locations

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

Study Contact

Study Locations

    • Tarsus
      • Mersin, Tarsus, Turkey, 33400
        • Recruiting
        • Tarsus State Hospital
        • Contact:
          • Abdulkadir Goz, MsC

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

Sampling Method

Probability Sample

Study Population

Female patients with Non Spesific Neck Pain

Description

Inclusion Criteria:

  • Having neck pain lasting more than 30 days and being diagnosed with non-specific neck pain
  • Having a score of 14/50 or above on the Neck Disability Index
  • Expressing neck pain as at least 3/10 points or above on the visual analog scale
  • Being 18 years or older
  • Female patients

Exclusion Criteria:

  • Previously diagnosed orthopedic diseases related to the spine
  • Undergoing surgical upper extremity surgery that may affect upper extremity functions
  • Being pregnant and having just given birth
  • Serious pathologies (such as cancer, spondylolisthesis, rheumatoid arthritis, kyphoscoliosis, scoliosis, etc., thoracic deformity or ankylosing spondylitis)
  • Symptoms of cervical spinal stenosis (such as incoordination of hands, arms and legs, bowel and bladder incontinence)
  • Radix compression (such as sensory changes, muscle weakness, or decreased reflexes)
  • History of whiplash or cervical surgery
  • Kyphoscoliosis, scoliosis etc. thorax deformity
  • Having a body mass index over 30

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Non Spesific Neck Pain
Patients with Non Spesific Neck Pain
upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life
Healthy Control
Individuals with similar age
upper extremity functions (hand skills, hand and finger grip strength, reaction time, position sense, upper extremity strength and endurance) and health-related quality of life

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
hand skills
Time Frame: 4 minutes
Assessed with Nine Hole Peg Test
4 minutes
hand grip strength
Time Frame: 1 minute
Assessed with Baseline Hand Dynamometer
1 minute
pinch grip strength
Time Frame: 1 minute
Assessed with Baseline Pinchmeter
1 minute
reaction time
Time Frame: 1 minute
Assessed with Nelson Hand Reaction Test
1 minute
position sense
Time Frame: 5 minutes
Assessed with Baseline Digital Inclinometer
5 minutes
Upper extremity strength and endurance
Time Frame: 1 minutes
Assessed with Single Arm Military Press Test
1 minutes
upper extremity disability
Time Frame: 5 minutes
Assessed with DASH questionnarie
5 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Health Related Quality of Life
Time Frame: 5 minutes
Assessed with SF36 quastionnarie
5 minutes
Neck disability
Time Frame: 5 minutes
Assessed with Neck Disability Index
5 minutes

Collaborators and Investigators

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

Collaborators

Investigators

  • Study Director: Sevgi OZALEVLİ, PhD, Dokuz Eylül University

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)

December 1, 2023

Primary Completion (Estimated)

June 1, 2025

Study Completion (Estimated)

September 1, 2025

Study Registration Dates

First Submitted

January 22, 2024

First Submitted That Met QC Criteria

January 22, 2024

First Posted (Estimated)

January 31, 2024

Study Record Updates

Last Update Posted (Estimated)

January 31, 2024

Last Update Submitted That Met QC Criteria

January 22, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DokuzEU01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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