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

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

Status
UNKNOWN
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04906681
Enrollment
40
Registered
2021-05-28
Start date
2021-09-01
Completion date
2022-07-01
Last updated
2021-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthroplasty, Neurologic Disorder

Keywords

rehabilitation, technology

Brief summary

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.

Interventions

DEVICEi-ACT

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

Sponsors

St-Trudo hospital, St-Truiden, Belgium
CollaboratorUNKNOWN
PXL University College
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Canadian Occupational Performance MeasureBaselineThe 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.

Secondary

MeasureTime frameDescription
System Usability Scale1 weekUsability of a system, in this i-ACT. Range of scores from 0 (negative) to 100 (positive).
Timed Up and Go testBaselineThe time between a person standing up from a chair, walking 3 meters before turning around and walking back to sit back in the chair.
Intrinsic Motivation Inventory1 weekThe Intrinsic Motivation Inventory (IMI) is a multidimensional measurement questionnaire intended to assess participants' subjective experience with, in this, i-ACT. The IMI consists of 6 subscales in which a person scores on a scale from 1 (totally not true) to 7 (totally true). Some scores need to be reversed by subtracting the response score from 8. A total IMI-score is not recommended, therefore subscale scores are used in the analyses. A higher score means a higher level of the aspect of the subscale.
Wolf Motor Function TestBaselineArm-hand functioning. The test contains 17 items and are scored from 0 (not able to perform tesk) to 5 (normal performance).
Barthel IndexBaselineThe Barthel Index measures the degree of assistance required by an individual on 10 items of mobility and self care ADL. Scores range from 0 to 100.
2 Minute Walking TestBaselineThis is a measure of the distance a person can walk in 2 minutes.

Contacts

Primary ContactEls Knippenberg, MSc
els.knippenberg@pxl.be+3211775225
Backup ContactFitore Bajrami, BSc
fitore.bajrami@stzh.be011 69 91 11

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026