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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05567861
Other study ID # 22-20
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 11, 2022
Est. completion date October 2023

Study information

Verified date December 2022
Source Centre Hospitalier Princesse Grace
Contact Jean-Marie AMODEO, MD
Phone 00 377 97 98 97 02
Email jmamodeo@chpg.mc
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Fibromyalgia is a frequent chronic pain syndrome almost often affecting women and associating diffuse chronic musculoskeletal pain (for more than 3 months), fatigue and sleep disturbances. Other varied functional symptoms are associated with it, in particular cognitive disorders and a feeling of unrested awakening. Technological advances in virtual reality have led to recognition by the medical community as a way to improve pain and quality of life for patients. There is a growing body of evidence supporting the use of virtual reality as an adjunct therapy to reduce acute pain in patients during medical procedures in hospital settings. There may also be a role for virtual reality in patients with chronic pain.


Description:

Current treatments for fibromyalgia (FM) include pharmaceutical pain medications as well as psychological programs with components of cognitive therapy, and activity management. However, pain medications are not fully effective, can be addictive, and can cause hyperalgesia. Non-pharmacological treatments for chronic pain may be associated with limiting side effects, technology-based interventions using virtual reality (VR) may be a promising alternative treatment option. There is evidence which shows that VR can be an effective treatment for pain reduction. However, most studies which utilize VR as a method of pain reduction focus on acute pain and studies looking at VR for chronic pain are scarce. Investigator will analyze the pain reduction and impact on behavioral mechanisms and cognition with repetitive active VR on Fibromyalgia


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date October 2023
Est. primary completion date September 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria : - Patients able to understand and sign the informed consent form for the study - Adults aged 18 to 65 years - Followed in algology for fibromyalgia pain > 6 months - With mean pain intensity = 4 Exclusion Criteria : - History of epilepsy or hypersensitivity to flashing light to limit the risk of virtual reality-induced seizures - Previous use of VR for pain (possible bias) - Refusal to participate - Therapeutic modifications for pain management related to fibromyalgia during the first month of participation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Monaco Centre Hospitalier Princesse Grace Monaco

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Princesse Grace

Country where clinical trial is conducted

Monaco, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient pain Numerical Rating Scale, 0 to 10, 0 = no pain, 10 = maximal pain month 1
Secondary Patient pain Numerical Rating Scale, 0 to 10, 0 = no pain, 10 = maximal pain week 2, month 2
Secondary Activity pain self-efficacy questionnaire, 0 to 60, 0 = not at all confident, 60 = completely confident month 1, month 2
Secondary Mood Hospital Anxiety and Depression scale, 0 to 42, 7 or less = no symptom, 8 to 10 = doubt on symptom, 11 and more = undeniable symptom month 1, month 2
Secondary Pain associated cognition Catastrophizing scale, 0 to 52, higher score indicates higher level of catastrophizing, a total score above 30 indicates clinically relevant level of catastrophizing month 1, month 2
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