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临床试验/NCT06924801
NCT06924801招募中不适用

Evaluating the Feasibility, Usability, and Integration of the OptiTrack Motion Capture System in Inpatient Physical Therapy

Stanford University1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年10月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
30
试验地点
1
主要终点
Evaluate the ease of use of Optitrack system measured by System Usability Scale (SUS)

研究概览

简要总结

Emerging technologies that utilize motion capture integrated with engaging software offer new methods for increasing engagement and movement in patients admitted to the hospital. Hospitalized patients are often limited to sedentary activities, spending the majority of their time in bed, which can contribute to deconditioning and functional mobility deficits. This study seeks to explore the feasibility of a tool designed to promote movement through engaging gameplay that is acceptable to both clinicians and families.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
6 Years 至 17 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Pediatric patients aged 6-17 years.
  • •Receiving physical therapy at Stanford Children's Hospital.
  • •Medically cleared for standing and upper-body movement.
  • •Ability to follow simple instructions and engage in standing gameplay

排除标准

  • •Orthopedic or medical conditions contraindicating physical activity.
  • •Legal guardian not present to obtain consent
  • •Child with a significant neurological condition or major developmental disability
  • •Child with active infection of the face or hand
  • •A history of severe motion sickness A history of seizures caused by flashing light Major surgery within the last 48 hours

研究组 & 干预措施

Pediatric patient

Experimental

Pediatric patient will engage with engagement-focused software platform (Snipperfingers) and movement will be analysed by the real-time motion capture system (the OptiTrack system).

干预措施: Snipperfingers (Behavioral)

结局指标

主要结局

Evaluate the ease of use of Optitrack system measured by System Usability Scale (SUS)

时间窗: Post-simulation (5 minutes)]

10-item questionnaire with a scale from 1- 5, 1 being strongly disagree to 5 being strongly agree on a five-point Likert scale to measure usability.

次要结局

  • Acceptability of Intervention Measure (AIM) survey(immediately after the intervention)
  • Intervention Appropriateness Measure (IAM) survey(immediately after the intervention)
  • Feasibility of Intervention Measure (FIM) survey(immediately after the intervention)
  • ISO 9241-400(immediately after intervention)
  • Setup time required for system use(Before intervention)
  • Duration of gameplay-driven physical activity(immediately at the start of intervention, immediately after intervention)
  • Evaluation parent's perception of patient's engagement.(immediately after intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas Caruso

Clinical Professor

Stanford University

研究点 (1)

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