NCT07511153

Brief Summary

The cervical spine is a complex structure that supports the weight of the head and protects the spinal cord and nerve roots. Cervical spinal stenosis (CSS), which develops as a result of degenerative processes, can cause narrowing of the spinal canal and compression of nerve structures, leading to symptoms such as pain, numbness, and weakness. This condition can negatively affect hand function, particularly grip strength and dexterity. However, studies in the literature examining the effect of CSS on grip strength and hand function are limited. Therefore, this study will be conducted to determine the effect of the severity of cervical spinal stenosis, identified in patients who underwent MRI following their presentation with cervical problems at the Physical Medicine and Rehabilitation outpatient clinic of Buca Seyfi Demirsoy Training and Research Hospital, İzmir Democracy University, on hand grip strength and functionality. Grip strength will be assessed using the Jamar hand dynamometer, and fine pinch strength will be evaluated using the Lafayette pinch meter. Additionally, hand functionality will be measured using the Nine-Hole Peg Test. The impact of neck pain on daily life will be assessed using the Neck Disability Index. The data obtained will be compared and analyzed using appropriate statistical methods. This study is expected to fill a significant gap in the current literature by comprehensively elucidating the effects of cervical stenosis on hand function and grip performance, thereby contributing to the individualization of rehabilitation approaches.

Trial Health

65
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Trial Health Score

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

Enrollment
180

participants targeted

Target at P50-P75 for all trials

Timeline
15mo left

Started Sep 2026

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

March 30, 2026

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 6, 2026

Completed
5 months until next milestone

Study Start

First participant enrolled

September 1, 2026

Expected
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2027

Last Updated

May 15, 2026

Status Verified

May 1, 2026

Enrollment Period

1 year

First QC Date

March 30, 2026

Last Update Submit

May 13, 2026

Conditions

Keywords

cervical spinal stenosishand grip strengthneck pain

Outcome Measures

Primary Outcomes (1)

  • Hand Grip Strength

    Hand grip strength will be assessed using a Jamar hydraulic hand dynamometer. Measurements will be taken while seated, with the arm positioned as follows: shoulder adduction, elbow at 90° flexion, and forearm in a neutral position. The wrist will be positioned at 0-30° extension and 0-15° ulnar deviation. The volunteer will be asked to grip the dynamometer firmly and squeeze as hard as possible. The measurements will be repeated three times, and the average value will be recorded in kilograms.

    Day 1

Secondary Outcomes (3)

  • Pinch Strength

    Day 1

  • The Nine-Hole Peg Test

    Day 1

  • Neck Disability Index

    Day 1

Study Arms (4)

1

Group with Kang grade 0

2

Group with Kang grade 1

3

Group with Kang grade 2

4

Group with Kang grade 3

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The sample for this study will consist of individuals who presented to the Physical Medicine and Rehabilitation outpatient clinic at the Buca Seyfi Demirsoy Training and Research Hospital of Izmir Democracy University due to cervical problems and underwent cervical MRI. After obtaining informed consent, the individuals included in the study will undergo evaluation. First, participants will be grouped based on their cervical stenosis scores. The degree of cervical stenosis will be determined using MRIs that were previously requested and performed during various outpatient services. The evaluation of the MRI will be scored according to the Kang grading system for spinal stenosis. The Kang grading system includes four degrees ranging from 0 to 3 based on spinal cord compression.

You may qualify if:

  • Individuals aged 18-75
  • Individuals who have previously undergone a cervical MRI
  • Cases where the degree of stenosis can be clearly determined on MRI
  • Individuals who have had neck pain for at least 3 months

You may not qualify if:

  • Individuals who declined to participate in the study
  • Individuals who had undergone cervical surgery
  • Individuals diagnosed with vertigo
  • Individuals with sudden hearing loss
  • Individuals with additional neurological conditions
  • Individuals with psychiatric or cognitive disorders that would prevent measurement in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Neck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Kadir Songür, Assoc. Prof.

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

March 30, 2026

First Posted

April 6, 2026

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

December 1, 2027

Last Updated

May 15, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Individual participant data (IPD) will not be shared because the data contain potentially identifiable sensitive clinical information, and sharing was not covered in the original informed consent provided to participants. Additionally, institutional and national data protection regulations limit the transfer of raw, de-identified individual-level data outside the research team.