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临床试验/NCT04699474
NCT04699474已完成不适用

Protocol for Rapid Onset of Mobilization in Patients With Traumatic Spinal Cord Injury (PROMPT-SCI)

Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal2 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2021年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
2
主要终点
Ambulation

研究概览

简要总结

PROMPT-SCI (Protocol for Rapid Onset of Mobilization in Patients with Traumatic SCI) is a single-site single-arm proof-of-concept trial. Forty-five patients aged 18 years or older who have sustained a severe traumatic SCI (American Spinal Injury Association Impairment Scale grade A, B or C) from C0 to L1 and undergoing spinal surgery within 48 hours of the injury will be included. Participants will receive daily 30-minute sessions of in-bed leg cycling for 14 consecutive days, initiated within 48 hours after spinal surgery. The feasibility outcomes consist of the 1) absence of serious adverse events associated with cycling sessions, 2) completion of at least 1 full session within 48 hours after spinal surgery for at least 90% of participants, and 3) completion of at least 11 sessions for at least 80% of participants. Patient outcomes 6 weeks and 6 months after injury will be measured from neurofunctional assessments, quality of life questionnaires and inpatient length of stay. Feasibility and patient outcomes will be analysed with descriptive statistics. Patient outcomes will also be compared to a matched historical cohort not receiving in-bed cycling.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Blunt traumatic spinal cord injury
  • Neurological level of injury from C0 to L2
  • American Spinal Injury Association impairment scale grade A, B or C
  • Spine surgery performed within 48 hours of injury

排除标准

  • Condition limiting patient's ability to engage into cycling
  • Medical condition that might interfere with patient's safety if cycling
  • Moderate or severe brain injury
  • Inability to walk independently prior to injury
  • Pre-existing neurological disorder
  • Complete spinal cord transection
  • Unwilling or unable to comply with scheduled follow-up

结局指标

主要结局

Ambulation

时间窗: 6 months

Independent walking (with or without device)

次要结局

  • Health related quality of life(6 months)
  • Neurological recovery(6 months)
  • Function(6 months)
  • Spasticity(6 months)

研究者

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

Jean-Marc Mac-Thiong

Principal Investigator

Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal

研究点 (2)

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