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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