Skip to content

Evaluation of the ELEMENTS tablet for post-stroke rehabilitation

Evaluation of the ELEMENTS tablet for rehabilitation of cognition and dexterity of the upper limb in post-stroke rehabilitation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12619001557123
Enrollment
19
Registered
2019-11-12
Start date
2019-11-25
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

None listed

Brief summary

We anticipate that participants recovering from stroke will be able to participate in inpatient and home-based ELEMENTS-T therapy effectively and will show enhanced motivation to engage in therapy as a result of their involvement. This will fulfil the principle that rehabilitation methods that encourage intense interaction are most beneficial. With the ELEMENTS-T system, intensity is ‘given for free’ because the therapy is fun and the benefits accrue incidentally as a function of active and playful interaction. We expect that the user interaction afforded by the system will enable inpatients to make significant gains in motor and cognitive function, compared to treatment as usual.

Interventions

The study is comprised of two cohorts: (1) hospital or inpatient based rehabilitation patients and (2) community based rehabilitation patients. Both cohorts will complete 30 min of individual therapy sessions (conventional or experimental), 3 times weekly, prescribed by a senior Occupational/Physical Therapist specialist. The inpatient cohort will complete the interventions for 4 weeks as an inpatient and then an additional 8 weeks once discharged into the community and will be supported by a

The study is comprised of two cohorts: (1) hospital or inpatient based rehabilitation patients and (2) community based rehabilitation patients. Both cohorts will complete 30 min of individual therapy sessions (conventional or experimental), 3 times weekly, prescribed by a senior Occupational/Physical Therapist specialist. The inpatient cohort will complete the interventions for 4 weeks as an inpatient and then an additional 8 weeks once discharged into the community and will be supported by a Specialist Occupational/Physical Therapist if and when required. The community based cohort will complete 8 weeks of therapy only and participants allocated to this group will complete all the therapy sessions in their own homes. For the experimental intervention we will use the ELEMENTS-T tablet, an electronic device containing a computer software providing a mix of goal-directed and exploratory upper-limb movement and cognitive interactive tasks. The software will provide exercises of moderate intensity. Adherence to the therapy program will be monitored and recorded online, participants will be contacted by phone if/when required. Participants will complete all therapy session in hospital (inpatient cohort) and later at home (Community based cohort). For the conventional intervention we will use the Graded Repetitive Arm Supplementary Program (GRASP), an evidence based exercise program designed for Stroke patients at the University of British Columbia https://neurorehab.med.ubc.ca/grasp/. This program provides a moderately intensive level of exercises and focus on part practice of the upper limb addressing strength, dexterity and rang of motion. Participants will keep track and evidence of adherence to this program on a table and will receive regular phone calls to assess and monitor adherence. Both cohorts will receive initially a 30 minute education session from a Senior Therapist and will be expected to complete the prescribed tasks in a self directed manner thereafter if able. Those participants requiring assistance with set up will have access to this from a family member or therapist, however they will be expected to complete all tasks with little to no intervention from another.

Sponsors

Australian Catholic University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

1. Aged 18 years and above 2. English speaking 3. Sustained an ischemic or haemorrhagic stroke, subsequently confirmed on routine neuroimaging 4. Admitted to the Rehabilitation Service of the Hospital (or respective hospital) for treatment of identified upper limb rehabilitation needs 5. Able to provide informed consent 6. At least partial active anti-gravity upper limb movement at shoulder, elbow and forearm.

Exclusion criteria

1. Previous history of neurologic or psychiatric disorder 2. Pre-existent dementia (standardised cut-off of at least 3.6 on the short Informant Questionnaire on Cognitive Decline in the Elderly 3. Receptive aphasia preventing comprehension of instructions 4. Visual acuity deficit that prevents perception of visual material 5. Lack of a contact telephone to arrange follow-up

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 14, 2026