Action Observation and Motor Imagery Training in Cervical Disc Herniation

NCT ID
NCT07781982
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
İrem Çetinkaya
Conditions
Cervical Disc Herniation, Cervical Pain, Chronic Pain, Kinesiophobia

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Clinical Effectiveness of Action Observation and Motor Imagery Training in Individuals With Cervical Disc Herniation

Enrollment: 36 participants (Estimated).

What is being studied

  • Other: Action Observation and Motor Imagery Training
  • Other: Conventional Physiotherapy
  • Other: Sham Observation

Who may be eligible

Ages
18 Years to 65 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: Adults aged 18 to 65 years. Diagnosis of cervical radiculopathy confirmed by a physician based on clinical examination and magnetic resonance imaging (MRI). History of chronic neck pain lasting at least 3 months. Sufficient active cervical range of motion to participate in the intervention (flexion and extension ≥20°, lateral flexion ≥15°, and rotation ≥30°). Neck pain intensity of ≥3 points on the Visual Analog Scale (VAS) and neck disability of ≥10 points on the Neck Disability Index (NDI) at baseline. Willingness to participate and provision of written informed consent. Exclusion Criteria: Inability to comply with the study protocol or cooperate with study procedures. Cognitive impairment (e.g., dementia or learning disability) that would interfere with understanding or completing the intervention or assessments. History of cervical spine surgery. Acute trauma, fracture, tumor, infection, or other serious pathology involving the cervical spine or shoulder region. Cervical spinal stenosis, cervical myelopathy, advanced cervical spondylosis, or other significant structural degenerative cervical spine disorders. Uncontrolled neurological or systemic disease that could influence study participation or outcomes. Receipt of any treatment targeting the cervical region within the previous 6 months (e.g., physiotherapy, injection therapy, or other invasive interventions). Visual impairment, hearing impairment, or severe vestibular disorders that would prevent participation in the intervention protocol.

Study locations

No study locations are listed in the registry data.

Study details

Start date
August 25, 2026
Primary completion date
November 1, 2026
Completion date
December 1, 2026
First posted
August 24, 2026
Collaborators
Halic University

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07781982
Registry last updated
August 24, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07781982 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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