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Acute Effects of Motor Imagery and Motor Control Exercises in Individuals With Chronic Neck Pain

Comparison of the Acute Effects of Motor Imagery and Motor Control Exercises in Individuals With Chronic Neck Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07487987
Enrollment
40
Registered
2026-03-23
Start date
2026-03-10
Completion date
2026-09-14
Last updated
2026-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Neck Pain

Brief summary

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.

Interventions

A single session of motor imagery exercise will be performed according to the PETTLEP model.

A single session of motor control exercise will be performed a

Sponsors

KTO Karatay University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Pain SeverityBaseline and immediately post-interventionThe 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.
Pressure Pain ThresholdBaseline and immediately post-interventionPressure 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).
Cervical proprioceptionBaseline and immediately post-interventionCervical 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.
Motor ImageryBaseline and immediately post-interventionMotor 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.

Countries

Turkey (Türkiye)

Contacts

CONTACTHasan Gerçek, PhD
hasangercek42@gmail.com+905426488455

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 3, 2026