Cost-Effectiveness Analysis of a Virtual Reality-Assisted Hypnotherapy Program on Quality of Life in Patients with Chronic Neck Pain: a Multicenter, Randomized, Prospective, Comparative, Open-Label, Parallel-Group Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Chronic Neck Pain
- Sponsor
- University of Beykent
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Change in Pain Intensity
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
This randomized, prospective study aims to evaluate the effectiveness and cost-efficiency of a Virtual Reality (VR)-assisted hypnotherapy program on quality of life in patients with chronic neck pain. The study compares a VR-assisted hypnotherapy group to a standard treatment group. Both groups will undergo a conventional physical therapy program supervised by physiotherapists for 3 weeks (15 sessions). The VR-assisted hypnotherapy group will receive additional sessions utilizing the HypnoVR software, which delivers relaxing virtual environments. Outcomes will be assessed immediately after treatment, at 1 month, and at 3 months post-treatment. Primary endpoints include pain reduction measured by the Visual Analog Scale (VAS). Secondary endpoints include functionality, quality of life, anxiety, depression, sleep quality, healthcare costs, and treatment adherence. Statistical analyses will determine the efficacy and economic impact of this innovative therapy for chronic neck pain management.
Investigators
TUĞBA ŞAHBAZ
Associate Professor
University of Beykent
Eligibility Criteria
Inclusion Criteria
- •Age between 50 and 80 years.
- •Chronic neck pain lasting for more than 3 months.
Exclusion Criteria
- •History of spinal surgery.
- •Beck Depression Inventory (BDI) score \>
- •Presence of neurological deficits or concurrent neurological diseases.
- •Medical conditions incompatible with the use of VR headsets (e.g., vision problems, epilepsy).
- •Pregnancy.
- •Recent changes in medication for chronic pain within the past 3 months (e.g.,- Pregabalin, Gabapentin, Duloxetine).
Outcomes
Primary Outcomes
Change in Pain Intensity
Time Frame: Assessed at baseline, immediately after treatment (3 weeks), and at 1- and 3-month follow-ups.
The primary outcome is the percentage change in pain intensity, measured using the Visual Analog Scale (VAS). A reduction of ≥30% in the VAS score from baseline is considered clinically significant.
Secondary Outcomes
- Change in Functional Status(Baseline, post-treatment (3 weeks), and at 1- and 3-month follow-ups.)
- Change in Quality of Life(Baseline, post-treatment (3 weeks), and at 1- and 3-month follow-ups.)
- Reduction in Analgesic Use(Baseline and weekly throughout the 3-month follow-up period.)
- Change in Anxiety and Depression Levels(Baseline, post-treatment (3 weeks), and at 1- and 3-month follow-ups.)
- Reduction in Healthcare Utilization(Assessed retrospectively at baseline and at the 3-month follow-up.)