Skip to content

A Virtual reality-Treadmill combined Intervention for enhancing Mobility and reducing falls in the Elderly (V-TIME)

A Virtual reality-Treadmill combined Intervention for enhancing Mobility and reducing falls in the Elderly (V-TIME) - V-TIME fall prevention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37232
Enrollment
40
Registered
2012-12-17
Start date
2013-01-18
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Memory problems Older fallers

Interventions

After consent, participants will be randomized to either *Treadmill Training with Virtual Reality* (TT+VR) or *Active control comparison of Treadmill Training alone* (TT). The training will be provi

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Older fallers and patients with MCI are eligible for participation if they meet all of the following inclusion criteria: ;• >=2 falls within the 6 months prior to the study • Aged 60-85 years • Able to walk at least 5 minutes unassisted • Adequate hearing and vision • Stable medication for >=1 month and anticipated for the next 6 months;The following criteria are specific for either the older fallers or the MCI group.;Specific for the older fallers: • Clinical Dementia Rating (CDR) score = 0.0;Specific for the patients with MCI: • Diagnosis of MCI; CDR score = 0.5

Exclusion criteria

Exclusion criteria: Older fallers and patients with MCI will be excluded from the study if they meet any of the following criteria: ;• Psychiatric co-morbidities (e.g., major depression - DSM IV criteria) • Clinical diagnosis of dementia (e.g., Alzheimer*s, vascular, etc.) • History of stroke, traumatic brain injury, brain tumour or other neurological disorders • Acute lower back or lower extremity pain, musculoskeletal injuries, peripheral neuropathy which restricts gait • Unstable medical condition including cardiovascular instability in past 6 months • Unable to comply with training • Cognitively impaired (

Design outcomes

Primary

MeasureTime frame
The primary outcome measure is fall incidence rate during the 6 month post-training follow-up period, as assessed with a falls calendar.

Secondary

MeasureTime frame
Secondary outcome measures include gait, cognition, mobility, health related quality of life and prefrontal activation during walking.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)