Does the Cervical Stenosis Affect Hand Function?
Does the Degree of Cervical Spinal Stenosis Affect Hand Function?
1 other identifier
observational
180
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2026
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
CompletedFirst Posted
Study publicly available on registry
April 6, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2027
Study Completion
Last participant's last visit for all outcomes
December 1, 2027
May 15, 2026
May 1, 2026
1 year
March 30, 2026
May 13, 2026
Conditions
Keywords
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
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
Condition Hierarchy (Ancestors)
Central Study Contacts
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.