Protocol for Rapid Onset of Mobilization in Patients With Traumatic Spinal Cord Injury III (PROMPT-SCI III) Trial (PROMPT-SCI III)
研究概览
详细说明
GOALS: This longitudinal cohort study will investigate the clinical benefits of early acute exercise therapy after mild spinal cord injury (SCI).
Primary hypothesis: Recovering independent walking 1 year after a mild SCI is more likely with early acute exercise therapy, in comparison with a historical cohort not exposed to early acute exercise therapy. An increase in the percentage of individuals recovering independent walking in the community from 35% to 55% will be considered as a clinically meaningful increase.
Secondary hypothesis: Acute complications, neurological recovery, functional independence, quality of life and care pathway are improved with early acute exercise therapy.
METHODS: For this 5-year study, 107 participants with mild acute traumatic SCI will be recruited. Participants will perform daily 30-minute sessions of seated cycling throughout acute care, starting within 2 days of their surgery to decompress the spinal cord. The immediate response to cycling will be monitored from physiological (hemodynamic and respiratory) and electrophysiological (electromyography and H-reflex testing in lower extremities) assessments. Independent walking in the community (primary outcome) is defined by the ability to walk 100 meters outdoors without technical aids or only with leg orthosis. Secondary outcomes include all complications occurring during acute care (particularly early spasticity, pneumonia, urinary tract infection and pressure injury) and the care pathway (discharge destination and length of stay), as well as neurological recovery, functional independence and quality of life 1 year after the SCI. Outcomes will be compared to a control cohort of patients with mild SCI who did not receive exercise therapy during acute care, and the association with electrophysiological measures will be assessed.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Jean-Marc Mac-Thiong, MD, PhD
- 电话号码:1+514-338-2222
- 邮箱:jean-marc.mac-thiong@umontreal.ca
研究联系人备份
- 姓名:Andreane Richard-Denis Richard-Denis, MD, MSc
- 电话号码:1+514-338-2222
- 邮箱:andreane.rdenis@umontreal.ca
学习地点
-
-
Quebec
-
Montreal、Quebec、加拿大、h4j1c5
- Hôpital du Sacré-Cœur de Montréal
-
接触:
- Lara Chawa
- 电话号码:1+514-338-2222
- 邮箱:lara.chawa.cnmtl@ssss.gouv.qc.ca
-
首席研究员:
- Jean-Marc Mac-Thiong, MD, PhD
-
首席研究员:
- Andreane Richard-Denis, MD, MSc
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- adults 18 years or older with non-penetrating traumatic SCI
- SCI severity AIS grade D (motor function preserved with most key muscles able to move against gravity)
- NLI between C0 and L2; and spine surgery performed within 48 hours of SCI
Exclusion Criteria:
- intubated and mechanically ventilated
- conditions interfering with patient safety or ability to undergo cycling
- body mass index 40 kg/m2 or less (to prevent "frog leg" position during cycling)
- moderate or severe traumatic brain injury
- hemodynamic instability
- pelvic or lower extremity
- injury with weight-bearing or mobilization restrictions
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Activity-based therapy
Participants will receive daily 30-minute continuous sessions of leg cycling in seated position throughout acute care, starting after surgery as soon as the patient is fit for cycling.
While the participant is seated in the armchair in the hospital room, a motorized under desk exerciser will be placed on the floor so that the feet are positioned comfortably on the pedals.
The exerciser will be positioned to ensure that maximal knee flexion during cycling will be 70 degrees.
Pedal straps are installed to secure the feet while pedaling.
Running shoes are provided to participants to prevent harmful pressure and/or friction on heels, and the risk of developing pressure injuries.
Participants will pedal at a target cadence of 40 revolutions per minute (RPM).Unless participants actively reach the target cadence of 40 RPM, motor assistance will be noted and titrated/adjusted by the research assistant until the target is reached.
|
Seated cycling using motorized under desk exerciser
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Score from Item 14 of the Spinal Cord Independence Measure ranging from a minimum of 0 to a maximum of 8 (a higher score means a better outcome)
大体时间:1 year
|
Ambulation in the community
|
1 year
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
并发症
大体时间:围手术期/围操作期
|
包括肺炎、尿路感染、压力性损伤、痉挛等急性并发症。
|
围手术期/围操作期
|
|
从基线到1年时美国脊髓损伤协会损伤分级量表等级改善一级的有无情况
大体时间:1年
|
基线时与1年时美国脊髓损伤协会损伤量表等级的差异
|
1年
|
|
存在或不存在神经性疼痛
大体时间:1年
|
国际脊髓损伤疼痛基础数据集
|
1年
|
|
从基线到1年期间运动评分是否改善5分
大体时间:1年
|
从基线到1年运动评分的变化
|
1年
|
|
从基线到1年时感觉评分改善或未改善10分
大体时间:1年
|
基线水平与1年后感官评分的差异
|
1年
|
|
从基线到1年时损伤神经节段水平改善或未改善2个节段
大体时间:1年
|
基线至1年期间神经损伤水平差异
|
1年
|
|
Total score of Spinal Cord Independence Measure ranging from a minimum of 0 to a maximum of 100 (a higher score means a better outcome)
大体时间:1 year
|
Functional independence
|
1 year
|
|
Frequence of spasms from Penn Spasm Frequency Scale ranging from a minimum of 0 to a maximum of 4 (a higher score means a worse outcome)
大体时间:1 year
|
Severity of spasticity
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1 year
|
|
Physical component score from Short-form 36 ranging from a minimum of 0 to a maximum of 100 (a higher score means a better outcome)
大体时间:1 year
|
Physical component of Health-related quality of life
|
1 year
|
|
Mental component score from Short-form 36 ranging from a minimum of 0 to a maximum of 100 (a higher score means a better outcome)
大体时间:1 year
|
Mental component of Health-related quality of life
|
1 year
|
合作者和调查者
调查人员
- 首席研究员:Jean-Marc Mac-Thiong, MD, PhD、Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- ciusss-nordmtl
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
药物和器械信息、研究文件
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研究美国 FDA 监管的设备产品
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