Skip to content

Effects of Motor Control Training on Brain Functional Networks in Patients with Cervical Spondylotic Radiculopathy: Based on Functional Near-Infrared Spectroscopy

Effects of Motor Control Training on Brain Functional Networks in Patients with Cervical Spondylotic Radiculopathy: Based on Functional Near-Infrared Spectroscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116453
Enrollment
Unknown
Registered
2026-01-09
Start date
2026-01-13
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Cervical spondylotic radiculopathy

Interventions

Control group:No clinical intervention will be conducted.
Experimental group:Motor control training

Sponsors

The Third Affiliated Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients with cervical spondylotic radiculopathy 1 Meet the diagnostic criteria for cervical spondylotic radiculopathy; 2 Aged between 20 and 50 years old, of any gender, and right-handed; 3 Have a Visual Analog Scale (VAS) score of >= 3; 4 Be able to correctly understand and clearly express their own wishes; 5 Volunteer to participate in the trial and sign an informed consent form. Control group 1 Aged between 20 and 50 years old, of any gender, and right-handed; 2 Have no uncomfortable symptoms such as neck pain or radiating pain, with a VAS score of 0; 3 Be able to correctly understand and clearly express their own wishes; 4 Volunteer to participate in the trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: Patients with cervical spondylotic radiculopathy (Exclusion Criteria) 1 Patients with upper limb pain and numbness caused by other diseases; 2 Those with a history of cervical trauma, surgery, or congenital malformations; 3 Pregnant or lactating women; 4 Those who have received cervical treatment within the past 2 weeks; 5 Those with other serious medical conditions; 6 Those intolerant to the treatment methods; 7 Those with poor compliance and cooperation. Control group (Exclusion Criteria) 1 Those with other serious medical conditions; 2 Pregnant or lactating women; 3 Those with poor compliance and cooperation.

Design outcomes

Primary

MeasureTime frame
data of functional near-infrared spectroscopy (fNIRS) ;

Secondary

MeasureTime frame
Neck Disability index (NDI);Self-Rating Depression Scale (SDS);Self-Rating Anxiety Scale (SAS);Visual analogue scale (VAS);

Countries

China

Contacts

Public ContactMashuai

The Third Affiliated Hospital of Shandong First Medical University

rehab2011@163.com+86 178 6052 7557

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026