跳至主要内容
临床试验/NCT04692311
NCT04692311已完成不适用

Motivation, Usability and Functionality of an Intelligent Activity-based Client-centred Training System in Neurological Rehabilitation: a Pilot Study

PXL University College0 个研究点目标入组 25 人开始时间: 2016年1月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
25
主要终点
Intrinsic Motivation Inventory

研究概览

简要总结

The pilot study was performed to evaluate the usability, credibility and expectancy of an intelligent, activity-based client-centred training system (i-ACT), and the motivation towards its use in neurological rehabilitation over a short period of time.

详细描述

A mixed-method study was performed in four rehabilitation centres in Belgium. An homogenous convenience sample was recruited among persons with central nervous system disorders.

Participants received 3 x 45 minutes of training with the i-ACT system during six weeks, additional to conventional care. The Canadian Occupational Performance Measure (COPM) was used to collect and evaluate patients' individual goals towards rehabilitation. These goals were discussed with the therapists before implementing movements and exercises for each patient in the i-ACT system.

The following demographic data were obtained from the medical files: age, gender, and diagnosis. Outcomes measures were collected at baseline (T0), after 2 (T1), 4 (T2) and 6 (T3) weeks of training and at 9 weeks follow-up (T4).

The primary outcome measures were the Intrinsic Motivation Inventory (IMI), the System Usability Scale (SUS), Credibility/Expectancy Questionnaire (CEQ), the Canadian Occupational Performance Measure (COPM), and Wolf Motor Function Test (WMFT). The secondary measures were the Manual Ability Measure-36 (MAM-36), Modified Fatigue Impact Scale (MFIS), Trunk Impairment Scale (TIS), and Active Range of Motion (AROM).

After final training with i-ACT, a semi-structured interview was performed to gather more information about the participants' perception towards i-ACT.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

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
  • a medical diagnosis of central nervous system disease
  • dysfunction in upper limb and/or core stability
  • Persons with multiple sclerosis (MS) had to be free of treatment with corticosteroids for one month.
  • Persons with stroke or spinal cord injury, had to be at least three months post injury.

排除标准

  • severe spasticity (when spasticity impedes movement)
  • severe cognitive impairment (person is not able to understand and follow instructions)
  • severe communicative impairment (person is not able to answer questions)
  • severe visual impairment (person is not able to see the television screen)
  • persons who use an electric wheelchair

结局指标

主要结局

Intrinsic Motivation Inventory

时间窗: 12 weeks (i.e. 6 weeks follow-up)

Motivation towards a therapy, in this i-ACT

Credibility/Expectancy Questionnaire

时间窗: 12 weeks (i.e. 6 weeks follow-up)

Credibility and expectancy of a training system, in this i-ACT. The range of scores on each subscale (i.e. credibility and expectancy) is 27.

Canadian Occupational Performance Measure

时间窗: 12 weeks (i.e. 6 weeks follow-up)

By means of a semi-structured interview, participants are asked to identify their 5 main goals in self-care, productivity and/or leisure. Scores range from 0 to 10 (best score) in each defined goal.

System Usability Scale

时间窗: 12 weeks (i.e. 6 weeks follow-up)

Usability of a system, in this i-ACT. Range of scores from 0 (negative) to 100 (positive).

Wolf Motor Function Test

时间窗: 12 weeks (i.e. 6 weeks follow-up)

Arm-hand functioning. The test contains 17 items and are scored from 0 (not able to perform tesk) to 5 (normal performance).

次要结局

  • Active Range of Motion(12 weeks (i.e. 6 weeks follow-up))
  • Modified Fatigue Impact Scale(12 weeks (i.e. 6 weeks follow-up))
  • Manual Ability Measure-36(12 weeks (i.e. 6 weeks follow-up))
  • Trunk Impairment Scale(12 weeks (i.e. 6 weeks follow-up))

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

Researcher

PXL University College

相似试验