NCT07282522

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.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
64

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
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

Study Start

First participant enrolled

October 24, 2025

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

December 2, 2025

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 3, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 15, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 12, 2026

Completed
Last Updated

December 22, 2025

Status Verified

December 1, 2025

Enrollment Period

1 month

First QC Date

December 2, 2025

Last Update Submit

December 15, 2025

Conditions

Outcome Measures

Primary Outcomes (4)

  • Upper extremity functionality

    Upper extremity functionality will be assessed using the Disabilities of the Arm, Shoulder, and Hand questionnaire and Purdue Pegboard Manual Dexterity Test.The total score ranges from 0 to 100, with higher scores indicating a higher level of upper extremity disability.

    24-48 hours

  • Pain Threshold and Tolerance Assessment

    Participants' pain threshold and tolerance to pressure are assessed using a digital algometer (JTech Medical Industries, ZEVEX Company).

    24-48 hours

  • Pain Assessment evaluates

    Pain Assessment evaluates the intensity of pain felt by patients in centimeters (cm) during different activities and time periods (rest, activity and night).

    24-48 hours

  • Somatosensory Perception Tests

    24-48 hours

Study Arms (2)

Individuals with SDH

Individuals with SDH are patients diagnosed with cervical disc herniation by a physical therapist.

Other: Somatosensory Perception TestsOther: The Visual Analog ScaleOther: Pain Threshold and Tolerance AssessmentOther: Upper extremity functionality

healthy participants.

Individuals with similar demographic characteristics who did not have any neck pain during the initial interview were considered healthy participants.

Other: Somatosensory Perception TestsOther: The Visual Analog ScaleOther: Pain Threshold and Tolerance AssessmentOther: Upper extremity functionality

Interventions

Tactile Localization Test The tactile localization test assesses touch perception. Finger Recognition Test The participant is asked to point to their finger, which has been touched with a pen, while their eyes are closed. Double-Touch Stimulus Perception Test This test is based on the identification of two separate stimuli presented simultaneously.

Individuals with SDHhealthy participants.

The Visual Analog Scale evaluates the intensity of pain felt by patients in different activities and time periods (rest, activity and night) in centimeters (cm).

Individuals with SDHhealthy participants.

Participants' pain threshold and tolerance to pressure are assessed using a digital algometer (JTech Medical Industries, ZEVEX Company).

Individuals with SDHhealthy participants.

Upper extremity functionality will be assessed using the DASH and Purdue Pegboard Manual Dexterity Test.

Individuals with SDHhealthy participants.

Eligibility Criteria

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

Cervical disc herniation and healthy individuals

You may qualify if:

  • For the control group, having no complaints of neck pain and not having any neck-related diagnosis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dilan Demirtas Karaoba

Iğdır, Iğdir, Turkey (Türkiye)

RECRUITING

MeSH Terms

Interventions

Pain Threshold

Intervention Hierarchy (Ancestors)

PainSensationNervous System Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
assistant professor

Study Record Dates

First Submitted

December 2, 2025

First Posted

December 15, 2025

Study Start

October 24, 2025

Primary Completion

December 3, 2025

Study Completion

March 12, 2026

Last Updated

December 22, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations