Does the Cervical Stenosis Affect Hand Function?

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorIzmir Democracy University

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Individuals who declined to participate in the study

Individuals who had undergone cervical surgery

Individuals diagnosed with vertigo

Individuals with sudden hearing loss

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

180 Participants
are grouped into 4 trial groups

Locations

This trial has no locations

Sponsors and collaborators