跳至主要内容
临床试验/NCT07035730
NCT07035730招募中不适用

Post-stroke Gait Rehabilitation With a Unilateral Hip Exoskeleton: Clinical and Neuromuscular Outcomes

Carmelo Chisari2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年7月7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
发起方
入组人数
20
试验地点
2
主要终点
Number of device-related adverse events

研究概览

简要总结

The goal of this clinical trial is to evaluate the safety, reliability, and short-term effectiveness of SHAJA-based training in improving walking velocity and endurance in post-stroke patients.

The main questions it aims to answer are:

  • Does the SHAJA-based training improve walking velocity and endurance in post-stroke patients compared to conventional gait training?
  • Is the SHAJA exoskeleton safe and reliable?

Researchers will compare the SHAJA-based training to a conventional gait training to see if the former works to improve walking ability.

Participants will:

  • Perform six SHAJA-assisted gait training sessions or six conventional gait training sessions
  • Perform five assessment sessions

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •cerebral stroke, at least 3 months from cerebral event
  • •ability to ambulate with no more than minimal contact assistance, even with aids (Functional Ambulation Classification, FAC >= 43)
  • •self-selected walking velocity in the range [0.3-0.85] m/s
  • •anthropometry consistent with the specifications of the tested devices
  • •gait impairments that may benefit from hip assistance, e.g. hip weakness in flexion and/or extension (Medical Research Council, MRC, Scale for Muscle Strength >2 and <5 for flexion and extension)

排除标准

  • •Modified Ashworth Scale >3 at the hip and/or ankle joints
  • •Poor cognitive skills (corrected Mini-Mental State Examination, MMSE < 21)
  • •inability to follow verbal 3 step commands
  • •severe aphasia causing inability to communicate with the investigators
  • •serious medical conditions (recent myocardial infarction in less than 3 months, uncontrolled congestive heart failure (CHF), uncontrolled hypertension, uncontrolled seizures)
  • •leg deep vein thrombosis less than 6 weeks ago
  • •other pre-existing neurological disorders (Parkinson's disease, Amyotrophic Lateral Sclerosis, Multiple Sclerosis, Dementia)
  • •severe anxiety or depression (State-Trait Anxiety Inventory-Y, STAI-Y > 44, and the Beck Depression Inventory-II, BDI-II > 19)
  • •severe osteoporosis
  • •severe hip / knee osteoarthritis with limitation of movement or significant pain
  • •use of a colostomy bag
  • •skin wounds, infection, or problems at device contact locations
  • •major orthopaedic surgery or fractures within the last 90 days (hip, knee, ankle, foot, spine)
  • •cardiac surgery within the last 3 months
  • •patient has recently or is currently participating in research that may influence, in PI's opinion, responses to study intervention
  • •pregnancy
  • •implanted cardiac devices, such as pacemakers or automatic defibrillators (AICD)
  • •use of assistive device that, in the PI's opinion, could interfere with SHAJA

研究组 & 干预措施

SHAJA first, then conventional

Experimental

Patients will perform the SHAJA-assisted gait training during the first period of the trial followed by a conventional gait training during the second period of the trial

干预措施: Unilateral hip exoskeleton (Device)

SHAJA first, then conventional

Experimental

Patients will perform the SHAJA-assisted gait training during the first period of the trial followed by a conventional gait training during the second period of the trial

干预措施: Conventional gait training (Behavioral)

Conventional first, then SHAJA

Experimental

Patients will perform the conventional gait training during the first period of the trial followed by a SHAJA-assisted gait training during the second period of the trial

干预措施: Unilateral hip exoskeleton (Device)

Conventional first, then SHAJA

Experimental

Patients will perform the conventional gait training during the first period of the trial followed by a SHAJA-assisted gait training during the second period of the trial

干预措施: Conventional gait training (Behavioral)

结局指标

主要结局

Number of device-related adverse events

时间窗: From the pre-training evaluation (T1) to the second post-training evaluation, about 3 months after T1

Documenting device hardware and software malfunctions

时间窗: From the pre-training evaluation (T1) to the second post-training evaluation, about 3 months after T1

Changes in self-selected walking velocity (m/s) pre vs post Conventional training and SHAJA-assisted training interventions assessed with the 10 Metre Walk Test

时间窗: From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1

Changes in fast walking velocity (m/s) pre vs post Conventional training and SHAJA-assisted training interventions assessed with the 10 Metre Walk Test

时间窗: From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1

Changes in the difference between self-selected and fast walking velocity (delta m/s) pre vs post Conventional training and SHAJA-assisted training interventions assessed with the 10 Metre Walk Test

时间窗: From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1

Changes in walking endurance (in minutes) pre vs post Conventional training and SHAJA-assisted training interventions assessed with a Walk Test

时间窗: From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1

次要结局

  • Changes in gait kinematics/kinetics pre vs post Conventional training and SHAJA-assisted training interventions assessed with a motion capture system(From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1)
  • Changes in the execution time of the Timed-Up-and-Go (TUG) test pre vs post Conventional training and SHAJA-assisted training interventions(From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1)
  • Changes in Berg Balance Scale pre vs post Conventional training and SHAJA-assisted training interventions(From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1)
  • Changes in Motricity Index for Lower Limb pre vs post Conventional training and SHAJA-assisted training interventions(From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1)
  • Changes in Modified Ashworth Scale (MAS) pre vs post Conventional training and SHAJA-assisted training interventions(From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1)
  • Changes in Functional Ambulation Classification (FAC) pre vs post Conventional training and SHAJA-assisted training interventions(From the pre-training evaluation (T1) to the follow up, about 14 weeks after T1)

研究者

发起方
Carmelo Chisari
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Carmelo Chisari

Associate Professor

University of Pisa

研究点 (2)

Loading locations...

相似试验

Post-stroke Gait Rehabilitation Using the SHAJA-R... | 临床试验