Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact
Recruiting Observational

A Clinical Study on the Efficacy of Cognitive Distraction Focus Relaxation Therapy Based on MR

NCT06290011 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2023-10-11
Last updated
2024-11-13

Condition(s) studied

Pain

Investigational drug(s) / intervention(s)

Pain key group

Pain key group: mixed real pain treatment software, pain treatment scenarios in MR

Study summary

A prospective, single blind, randomized, parallel controlled trial was conducted to evaluate the analgesic effect and safety of MR based "cognitive distraction focus relaxation therapy" in patients clinically diagnosed with chronic moderate to severe pain

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
No
Inclusion Criteria: 1. 18-85 years old male and female; 2. Patients clinically diagnosed with chronic pain; 3. Chronic pain lasts for more than 3 months; 4. The average intensity of pain in the past month is 40mm and above (VAS); 5. Willing to abide by the relevant regulations of the experiment; Exclusion Criteria: 1. Serious cognitive impairment; 2. Current or previous diagnosis of epilepsy, dementia, migraine or other neurological diseases may hinder the use of mixed reality or have adverse effects; 3. Symptoms of nausea or dizziness; 4. Sensitive to luminous screens; 5. No stereo vision or severe hearing impairment; 6. Eye, face or neck injuries, which hinder the comfortable use of glasses; 7. The evaluated patient GAD-7 questionnaire 10 points and above, PHQ-9 questionnaire 10 points or above; 8. Have used VR or MR and other related devices to treat pain; 9. Other clinical studies have been completed now or recently (the past 2 months); 10. Currently pregnant or planning to get pregnant during the study; 11. At present, or some immediate family members work in a digital health company or pharmaceutical company that provides acute and chronic pain treatment.

Primary outcome measure(s)

  • Visual Analogue Scale/Score(VAS) — 3 days
    VAS pain score criteria ((0-10 points) 0 Points: painless; 3 points below: have a slight pain, can tolerate; 4 points- -6 points: patients with pain and affect sleep, and can still tolerate; 7 points-10 points: the patient has gradually intense pain, the pain is unbearable, affect appetite, affect sleep.

Trial sites (1)

FacilityCityRegionStatus
Ke Ma Shanghai Yangpu Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06290011 on ClinicalTrials.gov ↗ ← All trials in China