Non-specific spinal related pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Men and women aged 18-80 years; 2.Patients with a clinical diagnosis of chronic spine-related pain; 3.Chronic pain lasting more than 3 months; 4.The average pain intensity in the past month is 4 points or above (BPI); 5.Willing to comply with the relevant regulations of the experiment; 6.Willing and able to sign informed consent.
Exclusion criteria
Exclusion criteria: 1.Severe cognitive impairment; 2.A current or previous diagnosis of epilepsy, dementia, migraine, or other neurological disorder may hinder the use of mixed reality or have adverse effects; 3.Symptoms of nausea or dizziness; 4.Sensitive to light-emitting screens; 5.No stereoscopic vision or severe hearing impairment; 6.Injuries to the eyes, face or neck that prevent comfortable use of glasses.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effective rate of pain relief; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain on Activity, Sleep, Stress and Mood Disturbance Scale (DVPRS-II);Effective in improving physiological function and sleep disorders;Effective in decrease pain catastrophize;incidence in screen vertigo; | — |
Countries
China
Contacts
West China Hospital of Sichuan University