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The effect of cognitive and cognitive-motor training on falls in older people

A randomised controlled trial on the effect of cognitive-only and cognitive-motor training on falls in older people: understanding physical, neuropsychological and neural mechanisms

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616001325493
Acronym
smart+/-step
Enrollment
769
Registered
2016-09-22
Start date
2016-11-10
Completion date
2019-06-21
Last updated
2021-01-18

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

Conditions

None listed

Brief summary

No studies have examined the potential for cognitive or cognitive-motor training to prevent falls in older people, despite good evidence of fall-related cognitive and physical improvements following both intervention types. We have developed and validated a home-based computerised training intervention that can be delivered identically, either while seated (cognitive) or while standing and undertaking balance exercises (cognitive+motor). This unique design will allow us to assess whether cognitive and cognitive+motor training can prevent falls, as well as the neural, physiological, physical and neuropsychological mechanisms behind the intervention effects. We will conduct a randomised controlled trial of 750 older people, to determine the effects of cognitive and cognitive+motor training, compared with a no-intervention control group, in preventing falls and related physical, cognitive and neurological measures in older people. We hypothesise both interventions will significantly prevent falls and fall-related measures of physical and cognitive functions. Any differential effects of the interventions will provide valuable insights into the intervention components required for efficacious fall prevention, and those required for neural, neuropsychological and physical benefits.

Interventions

The intervention involves home-based cognitive or motor+cognitive training in community dwelling older people. Participants will be randomised to one of 3 arms for a 12-month intervention duration. Arm 1 involves cognitive training (seated computer games) for 120 minutes per week . Arm 2 involves cognitive-motor training (playing computer games with the feet while standing and stepping) for 120 minutes per week. Arm 3 is the no-intervention control. The training interventions (arms 1 and 2) in

The intervention involves home-based cognitive or motor+cognitive training in community dwelling older people. Participants will be randomised to one of 3 arms for a 12-month intervention duration. Arm 1 involves cognitive training (seated computer games) for 120 minutes per week . Arm 2 involves cognitive-motor training (playing computer games with the feet while standing and stepping) for 120 minutes per week. Arm 3 is the no-intervention control. The training interventions (arms 1 and 2) involve home-based training with a custom built system of software (user interface and games), operating on a supplied personal computer and response device (touch pad for arm 1 or stepping mat for arm 2). Following a 1-hour session of instruction and safety check with a trained research assistant, participants will be asked to undertake training unsupervised in their home. Participants will receive a follow-up home visit at 4 weeks (~1 hour) to ensure safe use and progression of training and discuss any issues related to using the program (with the exception of those participants who were deemed safe at the first visit, are fully compliant in the first 4 weeks and report that they do not require a second visit, for whom a telephone call will replace the 4 week home visit). Upon trial commencement, arm 1 and 2 participants will be instructed to gradually increase their training dose from 40 min per week (week 1,2), to 60 min (week 3,4), 80 min (week 5,6), 100 min (week 7, 8) and 120 min from week 9 onwards. The training will be recommended to be split over 3 or 4 sessions during the week and compliance will be monitored via data transfer to a web application. Participants not engaging in the minimum weekly training dose (80 mins) for 2 consecutive weeks will be contacted by telephone to discuss any issues and to encourage adherence. Intensity and progression of intensity of training will be adjusted as performance improves and the participant moves through the inbuilt game levels. Support will be provided by telephone and additional home visits from the research staff may be requested for those experiencing difficulty. Intervention group participants will also receive a custom-designed 10-page booklet containing health-related information relevant to older adults (e.g. healthy eating, exercise, hydration, mental health, bone and joint health).

Sponsors

Dr Daina Sturnieks
Lead SponsorIndividual

Study design

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

Eligibility

Sex/Gender
All
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

- Aged 65 years and older - Community-dwelling - Independent in activities of daily living; - English-speaking - Able to walk 10m without the use of a walking aid - Willingness to give informed consent and comply with the study protocol

Exclusion criteria

- Cognitive impairment (Pfeiffer Short Portable Mental Status Questionnaire; score <8) - Acute psychiatric condition with psychosis - Progressive neurological condition (such as Parkinson’s disease, Multiple Sclerosis) - Unstable medical condition that would preclude safe participation - Unable to read a computer screen - Currently participating in a fall prevention research trial

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 20, 2026