Ignite Creation Date:
2024-10-26 @ 3:36 PM
Last Modification Date:
2024-10-26 @ 3:36 PM
Study NCT ID:
NCT06523361
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-07-04
Brief Title:
Contribution of Immersive Virtual Reality to a Standardized Rehabilitation Program for Upper Limb Chronic Pain A Single-Case Experimental Design Study
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Contribution of Immersive Virtual Reality to a Standardized Rehabilitation Program for Upper Limb Chronic Pain A Single-Case Experimental Design Study
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
ReVIDoC
Brief Summary:
Background Chronic pain represents a significant public health concern given its high prevalence and the substantial impact it has on the quality of life of many individuals affected There is no single universally effective medical treatment for chronic pain The gold standard for treatment is a multidisciplinary rehabilitation program Immersive virtual reality IVR represents a novel and promising approach to do rehabilitation offering the potential to enhance engagement and perception of movement
The objective of this study was to investigate the improvement of upper limb function in chronic pain patients using an IVR device in occupational therapy sessions during a rehabilitation program
Methods The study use a single-case experimental design SCED to investigate the efficacy of IVR device in improving upper limb function in patients with upper limb chronic pain The study was conducted in three phases baseline intervention and follow-up The SCED will be with multiple baseline across subjects whereby the patient serves as his own control A total of 12 participants will be included The virtual reality sessions will be conducted exclusively during the intervention phase The primary outcome measure will be the upper limb function as assessed by the Quick DASH Disabilities of the Arm Shoulder and Hand questionnaire Furthermore the intensity of pain will be quantified using a numeric scale and the pain self-efficacy will be evaluated using the Pain Self-Effacity Short Form Questionnaire
Expected results This method will allow for the comparison of phases within and between subjects to determine whether the IVR sessions improve the function assessed by the Quick DASH
Conclusion Further investigation is required to determine the potential benefits of using IVR for upper limb chronic pain rehabilitation with a particular focus on the development of precise protocols for its use in clinical settings
The objective of this study was to investigate the improvement of upper limb function in chronic pain patients using an IVR device in occupational therapy sessions during a rehabilitation program
Methods The study use a single-case experimental design SCED to investigate the efficacy of IVR device in improving upper limb function in patients with upper limb chronic pain The study was conducted in three phases baseline intervention and follow-up The SCED will be with multiple baseline across subjects whereby the patient serves as his own control A total of 12 participants will be included The virtual reality sessions will be conducted exclusively during the intervention phase The primary outcome measure will be the upper limb function as assessed by the Quick DASH Disabilities of the Arm Shoulder and Hand questionnaire Furthermore the intensity of pain will be quantified using a numeric scale and the pain self-efficacy will be evaluated using the Pain Self-Effacity Short Form Questionnaire
Expected results This method will allow for the comparison of phases within and between subjects to determine whether the IVR sessions improve the function assessed by the Quick DASH
Conclusion Further investigation is required to determine the potential benefits of using IVR for upper limb chronic pain rehabilitation with a particular focus on the development of precise protocols for its use in clinical settings
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None