跳至主要内容
临床试验/NCT07202975
NCT07202975尚未招募不适用

RE-SCALE: Rehabilitation Engagement and Scaled Access With eXtended Reality and Artificial Intelligence

Universitat Jaume I0 个研究点目标入组 314 人开始时间: 2027年1月1日最近更新:

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:

  1. To conduct a two-site randomized controlled trial (RCT) comparing XR rehabilitation with conventional group rehabilitation.
  2. To assess both short-term and long-term outcomes (pain intensity, disability, kinesiophobia).
  3. To monitor and improve adherence through ecological momentary assessment and intervention (EMA/EMI) using an app and activity trackers.
  4. To enhance motivation and engagement with gamification, social connectedness, and avatar-based interaction.
  5. 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

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

研究者

发起方
Universitat Jaume I
申办方类型
Other
责任方
Sponsor

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