- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07487987
Acute Effects of Motor Imagery and Motor Control Exercises in Individuals With Chronic Neck Pain
April 2, 2026 updated by: Hasan Gerçek, KTO Karatay University
Comparison of the Acute Effects of Motor Imagery and Motor Control Exercises in Individuals With Chronic Neck Pain
The aim of this study is to compare the effects of single-session motor imagery and motor control exercises on pain, pressure pain threshold, cervical proprioception, and motor imagery in individuals with chronic neck pain.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hasan Gerçek, PhD
- Phone Number: 05426488455
- Email: hasangercek42@gmail.com
Study Contact Backup
- Name: Hasan Gerçek, PhD
- Phone Number: +905426488455
- Email: hasangercek42@gmail.com
Study Locations
-
-
Karatay
-
Konya, Karatay, Turkey (Türkiye)
- Recruiting
- KTO Karatay University
-
Contact:
- Hasan Gerçek
- Phone Number: 05426488455
- Email: hasangercek42@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Neck pain lasting at least 12 weeks,
- VAS score of at least 3 cm,
- Standardized Mini Mental Test score of at least 24.
Exclusion Criteria:
- History of cervical surgery,
- neurological deficit,
- malignancy,
- rheumatic diseases,
- having received physical therapy for the neck region within the last 3 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Motor Imagery
A single session of motor imagery exercise will be performed according to the PETTLEP model.
|
A single session of motor imagery exercise will be performed according to the PETTLEP model.
|
|
Experimental: Motor Control
A single session of motor control exercise will be performed
|
A single session of motor control exercise will be performed a
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pressure Pain Threshold
Time Frame: Baseline and immediately post-intervention
|
Pressure Pain Threshold will be assessed using a digital pressure algometer.
The algometer probe (1 cm²) will be applied perpendicularly to the skin surface over predetermined anatomical points.
Pressure will be increased at a constant rate of approximately 1 kg/cm² per second.
Participants will be instructed to indicate the moment when the sensation of pressure first becomes painful.
The value at this point will be recorded as the PPT (kg/cm²).
|
Baseline and immediately post-intervention
|
|
Cervical proprioception
Time Frame: Baseline and immediately post-intervention
|
Cervical proprioception will be evaluated using the CROM Device.
The assessment will be performed by measuring joint position sense (JPS) error.
Participants will be seated in an upright position with feet flat on the floor.
The CROM device will be securely positioned on the participant's head according to the manufacturer's guidelines.
A target position (e.g., 30° cervical rotation or flexion) will be demonstrated by the examiner.
Participants will be asked to actively move their head to the target position, hold it for 3 seconds, return to the neutral position, and then attempt to reposition their head to the same target position with eyes closed.
|
Baseline and immediately post-intervention
|
|
Pain Severity
Time Frame: Baseline and immediately post-intervention
|
The rest, activity and night pains of the participants will be evaluated with a 10 cm Visual Analog Scale before the treatment and at the end of the application.
"0" means no pain, "10" means excruciating pain.
Results will be recorded in cm.
|
Baseline and immediately post-intervention
|
|
Motor Imagery
Time Frame: Baseline and immediately post-intervention
|
Motor imagery ability will be assessed using the Movement Imagery Questionnaire 3 (MIQ-3).
The questionnaire consists of items assessing visual imagery (clarity of the image) and kinesthetic imagery (intensity of the sensation).
Each item is scored on a 7-point scale (1 = very hard to imagine, 7 = very easy to imagine).
Subscale scores (visual and kinesthetic) and a total score will be calculated.
Higher scores indicate better motor imagery ability.
|
Baseline and immediately post-intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 10, 2026
Primary Completion (Estimated)
June 13, 2026
Study Completion (Estimated)
June 14, 2026
Study Registration Dates
First Submitted
March 10, 2026
First Submitted That Met QC Criteria
March 17, 2026
First Posted (Actual)
March 23, 2026
Study Record Updates
Last Update Posted (Actual)
April 8, 2026
Last Update Submitted That Met QC Criteria
April 2, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- KaratayUH17
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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-
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