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Pilot Study Concerning an Intelligent Activity-based Client-centred Training System in Neurorehabilitation

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04692311
Acronym
i-ACT
Enrollment
25
Registered
2020-12-31
Start date
2016-01-04
Completion date
2016-08-31
Last updated
2020-12-31

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

Conditions

Central Nervous System Diseases, Neurological Rehabilitation

Brief summary

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.

Detailed description

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. For quantitative data, within-group differences of all the assessments were analysed using Friedman's ANOVA and Wilcoxon signed-rank test. Alpha was set at 0.05; No Bonferroni correction was applied as it is not compulsory in an exploratory study and furthermore, results are regarded as hypothesis for further investigations. The qualitative data was collected and recorded with a voice recorder. No specific analysis was used as the interview collected data to support or oppose the findings of the quantitative data.

Interventions

DEVICEan intelligent client-centred task-oriented training

3 x 45min of training with i-ACT system

OTHERSemi-structured interview

Participants, patients and therapists, were invited to a semi-structured interview after training period.

Sponsors

Hasselt University
CollaboratorOTHER
Hogeschool West-Vlaanderen
CollaboratorUNKNOWN
Jessa Hospital
CollaboratorOTHER
Ziekenhuis Oost-Limburg
CollaboratorOTHER
Revalidatie & MS Centrum Overpelt
CollaboratorOTHER
Universitaire Ziekenhuizen KU Leuven
CollaboratorOTHER
PXL University College
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Mixed-method pilot study in which persons with central nervous system diseases and occupational therapists were included

Eligibility

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

Inclusion criteria

* 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.

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
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).
Intrinsic Motivation Inventory2 weeksMotivation towards a therapy, in this i-ACT
System Usability Scale2 weeksUsability of a system, in this i-ACT. Range of scores from 0 (negative) to 100 (positive).
Credibility/Expectancy Questionnaire2 weeksCredibility 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 MeasureBaselineBy 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.

Secondary

MeasureTime frameDescription
Modified Fatigue Impact ScaleBaselineFatigue. Twenty-one items ar scored on a 5-point Likert scale (range from 0, never, to 4, almost always). The higher the score the most impact fatigue has on the life of the person. .
Trunk Impairment ScaleBaselineTrunk impairment. Scores range from 0 (minimum) to 23. The higher the score the less motor impairment is present in the trunk.
Active Range of MotionBaselineActive range of motion
Manual Ability Measure-36BaselineManual ability. Scores range from 0 (impossible to perform) to 4 (easy to perform)

Outcome results

None listed

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