Clinical Trial on Deprescribing Associated With a Psychoeducational Program Using Virtual Reality for Patients With Chronic Pain and Central Sensitization

Launched by BADALONA SERVEIS ASSISTENCIALS · May 1, 2025

Keywords

ClinConnect Summary

This clinical trial is studying a program called REDOCVR, which aims to help people with chronic pain safely reduce their use of pain medications, particularly opioids. The program combines education, physical activities, and emotional support, all enhanced with virtual reality (VR) experiences that make learning engaging and enjoyable. Participants will work with healthcare professionals to gradually lower their medication doses while also focusing on improving their overall well-being and coping skills.

To be eligible for this trial, participants need to be adults aged 18 and older who have been living with chronic non-cancer pain for at least three months and show symptoms related to central sensitization, like emotional distress or fear of movement. They should be able to attend scheduled sessions and provide informed consent. Throughout the study, participants can expect to learn new skills, receive support, and track improvements in their pain management, emotional health, and quality of life. This trial is currently recruiting participants and aims to find effective ways to manage chronic pain in primary care settings.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Adults (≥18 years) diagnosed with chronic non-cancer pain persisting for at least 3 months
• • Assigned to one of the participating primary care centers
• • Presence of central sensitization symptoms, emotional distress, kinesophobia, or inadequate response to prior treatments
• • Capacity to provide informed consent and complete questionnaires
• Exclusion Criteria:
• • Acute pain conditions (duration \<3 months)
• • Severe psychiatric or cognitive impairment
• • Uncontrolled vertigo, epilepsy, or major visual/auditory impairments
• • Conditions contraindicating use of VR equipment
• • Inability to attend scheduled sessions