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Effect of affordable technology on physical activity levels and mobility outcomes in rehabilitation

Effect of the addition of affordable technology to usual care on physical activity levels and mobility outcomes in people with mobility limitations admitted to hospital for aged care and neurological rehabilitation compared to usual care alone

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000936628
Acronym
AMOUNT (Activity and MObility UsiNg Technology) rehabilitation trial
Enrollment
300
Registered
2014-09-02
Start date
2014-09-22
Completion date
2016-11-10
Last updated
2021-07-05

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

Conditions

None listed

Brief summary

Mobility limitation is common in rehabilitation patients and can be improved by well-designed exercise programs. Exercise in people with mobility limitation is associated with better functional outcomes if the exercises relate closely to functional movements required for daily task independence. The broad aim of this project is to enhance mobility outcomes for people undergoing aged care and neurological rehabilitation. The specific hypothesis of this trial is that the addition of technology-based interactive exercises involving feedback to usual care will lead to better mobility outcomes than usual care alone for people admitted to aged care and neurological rehabilitation wards with mobility limitations. This study also aims to assess the cost-effectiveness of the intervention compared with usual care, establish predictors of greater use of the technologies and enhance understanding of participant experiences of technology use with qualitative methods. Participants will be randomised into a control and intervention group (n=300). Both groups will include hospital patients undertaking a usual rehabilitation program and the intervention group will receive one extra 30 to 60-minute session per day of video and computer or tablet-based interactive exercises. After discharge from the inpatient stay, participants in the intervention group will be encouraged to continue using the technologies at home. The total duration of the intervention will be six months after randomisation. Participants will be loaned necessary technology and trained in the safe use and progression of the games/exercises during a home visit by therapy staff. Weekly support via telephone, email of videoconference will also be provided during this phase of the study. This support will aim to assist study participants to maintain motivation and will identify and address any barriers to technology use at home. A baseline assessment will be conducted and follow-up assessments will occur at 3 and 12 weeks and 6 months after randomisation.

Interventions

The intervention group will receive tailored technology use in addition to usual care. The research physiotherapist will determine the most appropriate intervention based on discussion with the clinical physiotherapist, baseline assessment, participant goals, and the technology suitable in accordance with the intervention protocol. In addition to usual therapy each participant will be asked to use the intervention technologies between 30 and 60 minutes daily for five or more days per week. Th

The intervention group will receive tailored technology use in addition to usual care. The research physiotherapist will determine the most appropriate intervention based on discussion with the clinical physiotherapist, baseline assessment, participant goals, and the technology suitable in accordance with the intervention protocol. In addition to usual therapy each participant will be asked to use the intervention technologies between 30 and 60 minutes daily for five or more days per week. The total duration of the intervention will be six months after randomisation and will incorporate both inpatient rehabilitation and post-discharge settings. The prescription of technology to target mobility and physical activity problems will include, but will not be limited to, the use of video, computer and tablet programs and applications to encourage structured exercise and other forms of physical activity as well as pedometers to monitor activity levels. The chosen technologies are all relatively low cost and will provide feedback on mobility task or physical activity performance or dose. Some of the technologies involve games. The research physiotherapist will choose the most appropriate technology/ies for an individual patient by following a protocol refined through pilot testing. The exercise protocol guide will be reviewed quarterly and any new technologies will be added throughout the trial. Each technology used 1) provides feedback about task performance; 2) facilitates individualised tailoring and progression of exercise or physical activity; 3) enables progress towards a functionally relevant goal(s) to be recorded and graphed; and 4) is relatively inexpensive. The research physiotherapist will teach participants to use the technology and will develop individualised exercise procedures to enable participants to use the technology safely outside of therapy times. If judged by staff to be safe to do so, participants will exercise unsupervised or with the supervision of family members/friends, nursing staff and hospital volunteers. After discharge from the inpatient stay, participants will be encouraged to continue using the technologies at home. Participants will be loaned necessary equipment (stand-alone devices or games consoles, installed by study staff) and trained in the safe use and progression of the games/exercises during a home visit by the research physiotherapist. Weekly support via telephone, email or videoconference will be provided during this phase of the study. This support will aim to assist study participants to maintain motivation and will identify and address any barriers to technology use at home. Up to five home visits will be provided to manage technology issues and/or progression. Goals will be set collaboratively with each participant and recorded and reviewed throughout the intervention phase. Practice sheets and information from some of the devices (e.g. game play time, number of steps walked) will be used to monitor the dose of the intervention.

Sponsors

The George Institute for Global Health, Sydney Medical School, The University of Sydney
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
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Admitted for rehabilitation or assessment at one of the 3 study sites with: *reduced mobility (Short Physical Performance Battery score of less than 12) *clinician-assessed capacity for improvement in mobility *likely life expectancy of more than 12 months *anticipated length of stay of greater than or equal to 10 days. *ability to maintain a standing position with 1 person assist as a minimum standard

Exclusion criteria

*marked cognitive impairment *insufficient English language skills to participate in rehabilitation and no available interpreter *inadequate vision to use the devices *medical condition precluding exercise (unstable cardiac disease, uncontrolled hypertension, uncontrolled metabolic diseases, large abdominal aortic aneurysm or a weight-bearing restriction) *lack of interest in the use of the technologies *anticipated discharge to nursing home *discharge location too far from study site to complete home visits and follow-up assessments

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 1, 2026