NCT05826730

Brief Summary

Neck pain is one of the most frequently investigated and common musculoskeletal disorders that cause disability in the community.If neck pain is due to multifactorial etiology, it is defined as non-specific neck pain.Eccentric exercises are used to increase muscle strength and muscle mass. Non-specific neck pain affects negatively and often leads to severe disability. Various rehabilitation techniques are available to reduce pain and disability and increase functional level. This study aimed to compare the pain and functional status of eccentric exercise training and home program exercise groups of people with non-specific neck pain.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
38

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 15, 2021

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2022

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

February 15, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2023

Completed
2 months until next milestone

First Posted

Study publicly available on registry

April 24, 2023

Completed
Last Updated

April 24, 2023

Status Verified

April 1, 2023

Enrollment Period

1 year

First QC Date

February 15, 2023

Last Update Submit

April 12, 2023

Conditions

Keywords

Neck painExerciseEccentric strengtheningPainDisability

Outcome Measures

Primary Outcomes (3)

  • Pain Characteristics

    Pain frequency, duration

    before 8 weeks and end of the 8 weeks.

  • Pain severity

    Visual analog scale-VAS

    before 8 weeks and end of the 8 weeks.

  • Mcgill- Melzack Pain Questionnaire

    Mcgill- Melzack Pain Questionnaire

    before 8 weeks and end of the 8 weeks.the 24 session.

Secondary Outcomes (3)

  • Disability

    before 8 weeks and end of the 8 weeks.

  • Hand grip strength

    before 8 weeks and end of the 8 weeks.

  • Skin resistance

    before 8 weeks and end of the 8 weeks.

Study Arms (2)

Exercise

ACTIVE COMPARATOR

Eccentric muscle training for neck muscles

Other: Eccentric Exercises

Control

NO INTERVENTION

Home exercise program for neck muscles

Interventions

Eccentric Exercises for neck muscles.

Exercise

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • diagnosed with Non-Specific neck pain by a physician
  • Having a complaint of non-specific neck pain for at least 3 months
  • Neck pain severity \>40mm according to VAS
  • Voluntary participation of the individual in the study

You may not qualify if:

  • Radiculopathy and structural defect in the cervical region,
  • Surgical history on the cervical region,
  • Inflammatory disease,
  • Severe psychological illness,
  • Presence of infection in bone and soft tissue in the cervical spine,
  • Malignancy,
  • Advanced osteoporosis,
  • Having upper extremity pathologies,
  • Having a neurological disease that will prevent treatment
  • Having previously undergone cervical region and spine surgery
  • To be included in the physiotherapy program from the neck and back region in the last 6 months,
  • In case of administration of drugs such as NSAIDs, opioids in the last 24 hours

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Physiotherapy and Rehabilitation, Faculty of Health Sciences, Istinye University

Istanbul, 34010, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Neck PainMotor ActivityPain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized-controlled study
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 15, 2023

First Posted

April 24, 2023

Study Start

September 15, 2021

Primary Completion

September 30, 2022

Study Completion

February 15, 2023

Last Updated

April 24, 2023

Record last verified: 2023-04

Data Sharing

IPD Sharing
Will not share

no sharing of any participant's data

Locations