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Effectiveness of Remote Graded Motor Imagery Therapy for Patients with Central Sensitization Low Back Pain: Study Protocol for a Randomized Controlled Trial

Effectiveness of Remote Graded Motor Imagery Therapy for Patients with Central Sensitization Low Back Pain: Study Protocol for a Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084205
Enrollment
Unknown
Registered
2024-05-13
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Central Sensitization Low Back Pain

Interventions

intervention group 1:Remote Graded Motor Imagery Therapy
intervention group 2:Clinic offline graded motor imagery therapy

Sponsors

Shanghai University of Sport
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Age range: 20 to 50 years; (2) Duration of symptoms: suffering from chronic low back pain for more than six months; (3) Pain characteristics: the pain is not caused by recent acute trauma and is non-specific, primarily localized in the lumbar region; (4) Treatment history: poor response to conventional physical therapy and pain management within the past six months; (5) Cognitive and physical capabilities: sufficient cognitive and physical ability to adhere to the research protocol, including participation in remote therapy sessions; (6) Technological access and skills: capability to access necessary technology (such as a computer or tablet with internet connection) and possess basic operational skills to participate in remote therapy sessions; (7) Perceptual cognitive assessment: accuracy below 80% on a left/right discrimination test using the "Recognize" application.

Exclusion criteria

Exclusion criteria: (1) Specific spinal pathology; (2) Recent imaging confirming specific lumbar spine pathologies such as herniated discs, spinal stenosis, or spondylolisthesis; (3) Surgical history: history of spinal surgery within the past year; (4) Severe mental illness: diagnosed with severe depression, schizophrenia, or other mental health conditions that may hinder participation in therapy; (5) Other significant pain disorders: diagnosed with fibromyalgia, Complex Regional Pain Syndrome, or other chronic pain conditions that might interfere with treatment outcomes; (6) Current high pain level: a Visual Analog Scale (VAS) score greater than 7, indicating a high baseline level of pain; (7) Neurological disorders: any condition affecting motor control or sensory perception, such as multiple sclerosis or Parkinson’s disease; (8) Pregnancy: current pregnancy, as it may affect pain perception and physical capabilities.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS) ;Oswestry Disability Index (ODI);Pain Sensitivity Questionnaire (PSQ);

Secondary

MeasureTime frame
SF-36 Health Survey Questionnaire;Adverse Events in GMI Training;Physical Interferences or Impacts on Online Group Training;

Countries

China

Contacts

Public ContactHaoyu Hu

Shanghai University of Sport

472943082@qq.com+86 182 6263 0227

Outcome results

None listed

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