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Feasibility of INteractive Digital Technology (FIND) Technology

A randomised controlled trial on the feasibility and effect on physical activity and functional mobility of the additional use of Interactive Digital Technology compared to usual care in stroke survivors undergoing rehabilitation

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000427673
Acronym
FIND Technology
Enrollment
79
Registered
2014-04-17
Start date
2014-11-04
Completion date
2016-07-21
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The purpose is to investigate whether interactive digital technology (using the Xbox Kinect system) is feasable to use to improve the volume of activity that stroke survivors can undertake, and to determine if there are benefits to upper limb function or mobility using this technology

Interventions

The intervention will be participation in interactive computer based activities using the kinect system and software designed for stroke rehabilitation for up to 50 minutes up to 5 times per week during inpatient rehabilitation stay (2-8 weeks). Sessions will be supervised by a physiotherapist or occupational therapist, and attendance recorded. The software records duration and activities particpated in. This will be in addition to usual care 1;1 treatment on the ward by the ward physiotherapis

The intervention will be participation in interactive computer based activities using the kinect system and software designed for stroke rehabilitation for up to 50 minutes up to 5 times per week during inpatient rehabilitation stay (2-8 weeks). Sessions will be supervised by a physiotherapist or occupational therapist, and attendance recorded. The software records duration and activities particpated in. This will be in addition to usual care 1;1 treatment on the ward by the ward physiotherapist

Sponsors

The University of Tasmania
Lead SponsorUniversity

Study design

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

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No

Inclusion criteria

Inpatients on the Rehabiliation ward at the local hospital Stroke<6 months ago Reduced mobility Clinician assessed capacity to improve Life expectancy >12 months

Exclusion criteria

Cognitive impairment (for example MMSE,21) Insufficient English Medical condition precluding exercise (eg unstable cardiac disease, uncontrolled metabolic disease or weight bearing restriction) Receptive Aphasia

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 13, 2026