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临床试验/NCT04906681
NCT04906681Unknown1 期

Implementation of a Rehabilitation Technology in Orthopedic and Neurological Rehabilitation to Increase Therapy Dosage: an Exploratory Study

PXL University College0 个研究点目标入组 40 人开始时间: 2021年9月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
40
主要终点
Canadian Occupational Performance Measure

研究概览

简要总结

Rehabilitation technology is more and more implemented in conventional therapy to increase the dosage of therapy and/or increase patient's motivation towards therapy. In orthopedic as well as neurological rehabilitation it is important to exercise with enough intensity and repetitions to improve functional performance in activities of daily life, and consequently quality of life. At the moment, not all (rehabilitation) technologies are adapted towards the wishes and needs of both patients and therapists for everyday use in the clinical setting. Also, not all technologies are fit for independent use by the patients. Researcher of PXL have developed a Kinect-based system (i.e. i-ACT) for rehabilitation and performed supervised research with i-ACT in neurological and musculoskeletal rehabilitation, and older adults. Within this research, patients will exercise with i-ACT under supervision of their therapist during weekdays, but in the weekends they will be motivated by the medical staff to perform their exercises with i-ACT. The medical staff will be present for safety reasons, but the patient is asked to use and exercise with i-ACT as independent as possible. The aim of this research is to explore to which extend i-ACT is suitable for semi-independent use by patients in orthopedic or neurological rehabilitation.

研究设计

研究类型
Interventional
分配方式
Non 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 over 18 years old
  • post-operation of arthroplasty (hip or knee), or official medical diagnosis of stroke or Parkinson's disease
  • understand Dutch instructions
  • patient at St-Trudo ziekenhuis
  • experiencing problems in functional performance

排除标准

  • spasticity (Brunström Fugl-Meyer < 50)
  • cognitive disfunction (Mini Mental State Examination < 24)
  • visual impairment (blind, cataract, etc.)
  • persons who are not able to exit electric wheelchair

结局指标

主要结局

Canadian Occupational Performance Measure

时间窗: 4 weeks

The Canadian Occupational Performance Measure (COPM) is an evidence-based outcome measure designed to capture a client's self-perception of performance in everyday living, over time. Scores range from 0 to 10 (best score) in each defined goal.

次要结局

  • 2 Minute Walking Test(4 weeks)
  • Intrinsic Motivation Inventory(4 weeks)
  • Wolf Motor Function Test(4 weeks)
  • Barthel Index(4 weeks)
  • System Usability Scale(4 weeks)
  • Timed Up and Go test(4 weeks)

研究者

发起方
PXL University College
申办方类型
Other
责任方
Principal Investigator
主要研究者

Els Knippenberg

Principal investigator

PXL University College

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