← Back to Clinical Trials
Recruiting NCT07282522

NCT07282522 Sensory and Functional Impairments in Cervical Disc Herniation

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07282522
Status Recruiting
Phase
Sponsor Inonu University
Condition Cervical Disc Herniation
Study Type OBSERVATIONAL
Enrollment 64 participants
Start Date 2025-10-24
Primary Completion 2025-12-03

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 65 Years
Study Type OBSERVATIONAL
Interventions
Somatosensory Perception TestsThe Visual Analog ScalePain Threshold and Tolerance Assessment

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 64 participants in total. It began in 2025-10-24 with a primary completion date of 2025-12-03.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The aim of the study was to evaluate the levels of somatosensory perception, pain threshold and kinesiophobia in individuals with SDH, to examine their relationship with upper extremity functional skills and to compare them with healthy individuals.

Eligibility Criteria

Inclusion criteria for volunteers in the study: Neck pain lasting at least 3 months, Being between the ages of 18-65 with a diagnosis of cervical disc herniation, Being able to cooperate with the applied parameters, Having good cognitive function, Being literate, Agreeing to participate in the study. For the control group, having no complaints of neck pain and not having any neck-related diagnosis. Exclusion criteria for volunteers in the study: Neck pain intensity during activity according to the Visual Analog Scale (VAS) below 3, Individuals who have undergone any surgery related to neck problems, Individuals who have undergone surgery related to upper extremity problems, Individuals with cervical radiculopathy, Having a systemic malignant disease anywhere in the body, Having any disease related to connective tissue or inflammatory rheumatic diseases, Having a psychiatric diagnosis and receiving treatment, Being illiterate, Not having sufficient cognitive function, Having received any neck-related physical therapy in the last 6 months for the CBA group.

Frequently Asked Questions

Who can join the NCT07282522 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 65 Years, studying Cervical Disc Herniation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07282522 currently recruiting?

Yes, NCT07282522 is actively recruiting participants. Visit ClinicalTrials.gov or contact Inonu University to inquire about joining.

Where is the NCT07282522 trial being conducted?

This trial is being conducted at Iğdır, Turkey (Türkiye).

Who is sponsoring the NCT07282522 clinical trial?

NCT07282522 is sponsored by Inonu University. The trial plans to enroll 64 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology