RE-SCALE: Rehabilitation Engagement and Scaled Access With eXtended Reality and Artificial Intelligence
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 314
- 主要终点
- Pain intensity by VAS (0-100mm)
研究概览
简要总结
Background Chronic musculoskeletal pain, especially chronic low back pain (CLBP), is the leading cause of disability worldwide, with a burden expected to rise due to aging and increased longevity. Despite strong evidence supporting multimodal and non-pharmacological management-particularly active physical therapy and self-management-clinical practice still shows low adherence to guidelines, with excessive reliance on imaging, rest, injections, and surgery.
Adherence to physical therapy remains one of the most significant barriers: only 40-50% of patients follow prescribed exercise programs. Factors include kinesiophobia, low motivation, and logistical obstacles. Mixed realities (XR: VR, AR, MR) offer solutions by enhancing motivation, reducing barriers, and personalizing rehabilitation. Evidence from systematic reviews shows VR-based rehabilitation can reduce pain, disability, and kinesiophobia, with immersive VR offering additional benefits like presence and habit-building.
The SHARESPACE project developed and tested a novel XR rehabilitation environment for CLBP that integrates immersive VR/AR, tele-rehabilitation, real-time motor tracking, avatars for social support, and cognitive architectures for synchronization. Usability studies with patients, clinicians, and the general population confirm its feasibility and acceptance. SHARESPACE has completed phases 1 and 2 of XR intervention development (design and feasibility), now aiming to move to phase 3: large-scale clinical validation.
Objectives The main goal is to evaluate not only short-term efficacy but long-term, as well as including more accurate and objective measures. A second objective is the commercial exploitation WE will valuate the efficacy, adherence, and cost-effectiveness of the SHARESPACE XR rehabilitation system compared to usual care in patients with CLBP.
Specific objectives include:
- To conduct a two-site randomized controlled trial (RCT) comparing XR rehabilitation with conventional group rehabilitation.
- To assess both short-term and long-term outcomes (pain intensity, disability, kinesiophobia).
- To monitor and improve adherence through ecological momentary assessment and intervention (EMA/EMI) using an app and activity trackers.
- To enhance motivation and engagement with gamification, social connectedness, and avatar-based interaction.
- To generate evidence for commercial exploitation and integration into health systems.
Methodology
The project will conduct a two-site RCT with CLBP patients. Participants will be randomly allocated to:
-
XR rehabilitation:
-
Two hospital sessions (traditional + XR-assisted training).
-
Four remote XR sessions with therapist and patients (L1 avatars).
-
Continued home-based XR with automated therapist avatars (L3) for up to 120 days.
-
Integration of EMA/EMI via an app and wearable devices to monitor daily activity, sleep, and adherence, with automated prompts to encourage compliance.
-
Usual care: standard group rehabilitation sessions for 8 weeks.
Primary outcomes:
- Pain intensity (VAS, BPI).
- Disability (Oswestry Disability Index).
- Kinesiophobia (Tampa Scale of Kinesiophobia). Secondary outcomes: adherence rates, motivation, patient satisfaction, feasibility, and cost-effectiveness. Motor performance data will be captured in real time via XR tracking and transmitted to therapists for feedback.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age range: Adults over 18 and under 70
- •Diagnosis of chronic low back pain with or without radiculopathy
- •Minimum of moderate disability (21% ODI score)
- •Acceptance of participation and signed consent form
- •Internet access at home
排除标准
- •History of spinal surgery or fracture
- •Signs of upper motor neuron injury: bilateral paresthesia, hyperreflexia, or spasticity, or other negative signs such as fractures
- •Other severe medical or psychological conditions that prevent participation in the trial.
结局指标
主要结局
Pain intensity by VAS (0-100mm)
时间窗: Baseline, through study completion, an average of 8 week and follow-up at 6, 12 and 18
Significant change at 25 mm
Pain intensity by Brief Pain Inventory
时间窗: Baseline, through study completion, an average of 8 week and follow-up at 6, 12 and 18
Pain disability by Oswestry Disability Index (ODI)
时间窗: Baseline, through study completion, an average of 8 week and follow-up at 6, 12 and 18
Pain Kinesiophobia by Tampa Scale of Kinesiophobia (TSK)
时间窗: Baseline, through study completion, an average of 8 week and follow-up at 6, 12 and 18
次要结局
未报告次要终点
