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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1/PHASE2

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-01

Study Completion Date

2022-07-01

Brief Summary

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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.

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Detailed Description

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Conditions

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Arthroplasty Neurologic Disorder

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Arthroplasty, hip or knee

Minimum 5x/week (of which minimal 3x/week with therapists and 2x/week during weekend), 30-60 minutes training, for 4 weeks, with i-ACT system. i-ACT provides individualised exercises based on patients own goalsetting.

Group Type EXPERIMENTAL

i-ACT

Intervention Type DEVICE

i-ACT is a Microsoft Kinect-based system that provides individualised exercises based on patients own goalsetting.

Neurology: stroke or Parkinson disease

Minimum 5x/week (of which minimal 3x/week with therapists and 2x/week during weekend), 30-60 minutes training, for 4 weeks, with i-ACT system. i-ACT provides individualised exercises based on patients own goalsetting.

Group Type EXPERIMENTAL

i-ACT

Intervention Type DEVICE

i-ACT is a Microsoft Kinect-based system that provides individualised exercises based on patients own goalsetting.

Interventions

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i-ACT

i-ACT is a Microsoft Kinect-based system that provides individualised exercises based on patients own goalsetting.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* neglect
* 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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No