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Development and Validation of a Smart Phone Based System to Enhance Gait, Cognition and Socialization in Elderly Fallers

Development and Validation of a Smart Phone Based System to Enhance Gait, Cognition and Socialization in Elderly Fallers

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02769182
Enrollment
80
Registered
2016-05-11
Start date
2016-05-31
Completion date
Unknown
Last updated
2016-05-11

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

Conditions

Older Adults

Keywords

Older adults, falls, cognition, smart phone

Brief summary

The main objective of this research is to develop and validate a technology-based solution that addresses the diminished mobility, increased fall risk and impaired cognitive function that are so common among older adults, enabling them to live longer successfully and independently.

Detailed description

A comprehensive system will be developed to promote mobility, enhance cognitive function, reduce sedentary behavior, increase independence and encourage social inclusion. This novel system will have two distinct yet complementary features: monitoring and treatment that will serve as an all in one system. The system will consist of wearable sensors and a proprietary developed application. The wearable inertial sensors will measure the acceleration and orientation of the feet during movement. The sensors will feed real-time data to the system, which will process this data using a set of proprietary algorithms enabling continuous monitoring of activity, gait and fall risk, and independence. In addition, designated applications for direct cognitive assessment and training of older adults in their home and community environment will also be used via the Smart phone or mobile tablet. The training, both physical and cognitive, will also include multi-user interactions .Data collected by the system will be processed and integrated to provide comprehensive feedback from multiple domains to the user, caregiver and clinician by way of recommendations and personalized treatment goals.

Interventions

DEVICEMonitoring and training using the system

subjects and caregivers will be trained on using the system and receive a 'user manual' delineating all procedures and possible applications of the system, as well as operations for daily charging of the sensors and smart phone. They will then be fitted with the sensors. The clinician will set all necessary applications, including setting the cognitive games application and the 'network of users'. Users and care givers will be informed of the personalized recommendations system that will provide the user with daily feedback on activity and weekly recommendations and goals for duration of the study. A helpline will be provided in case technological problems occur or for routine support.

BEHAVIORALStandard of care

Subjects in this group will not receive the system but will encouraged to continue with their daily living routine and provided with recommendations for stretching and strengthening exercises. The control group subjects will be assessed at the same three time points as those in the experimental group. Subjects in both groups will also receive written information about the importance of activity, cognitive enhancing tasks, avoidance of falls and home hazards. In Israel, this information combined with an exercise prescription is considered the 'standard of care' for community-dwelling older adults.

Sponsors

HIT Holon Institute of Technology
CollaboratorUNKNOWN
Tel-Aviv Sourasky Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
65 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* Ages of 65-85 years * History of 1 fall or more in the year prior to the study.

Exclusion criteria

* Signs of dementia : Montreal Cognitive Assessment (MoCa) \<21 and/or mini mental state examination(MMSE) \<24. * Psychiatric co-morbidities :major depression as determined by Diagnostic and Statistical Manual of Mental Disorders (DSM) IV criteria * Co-existing somatic disorders * History of stroke * Neurologic disorders that interferes with normal walking (e.g., Parkinson's disease or Alzheimer's disease), * Cannot walk without assistance, * Severe head trauma or brain tumor, * Severe hearing or visual loss (determined by the visual acuity test), * Cardio-vascular contradictions (as determined by a physician), * Inability to use a Smart phone because of visual and manual impairment or have unstable medical conditions.

Design outcomes

Primary

MeasureTime frameDescription
Change in average number of steps per dayNumber of steps will be measured during one week after each assessment - at baseline, immediately after the training and 3 months after the training.This will be evaluated by a small, lightweight waterproof accelerometer placed on the lower back of the participants (Axivity Ltd.)
Changes in the color Trails Making Test part BAt baseline, immediately after the training and 3 months after completing the training.

Secondary

MeasureTime frameDescription
Changes in enduranceAt baseline, immediately after the training and 3 months after completing the trainingTotal distance walked in six minutes (6MWT).
Changes in social connectednessAt baseline, immediately after the training and 3 months after completing the trainingSocial engagement: the Berkman-Syme Social Network Index
Changes in cognitive function: score in Frontal Assessment BatteryAt baseline, immediately after the training and 3 months after completing the trainingFrontal Assessment Battery: this battery is sensitive to frontal lobe dysfunction consists of six subtests exploring the following: conceptualization, mental flexibility, motor programming, sensitivity to interference, inhibitory control, and environmental autonomy. It takes approximately 10 minutes to administer.
Changes in functional mobility: dynamic gait index (DGI) scoreAt baseline, immediately after the training and 3 months after completing the trainingDGI is a clinical tool to assess gait, balance and fall risk. It evaluates not only usual steady-state walking, but also walking during more challenging tasks
Changes in the Short Form Health SurveyAt baseline, immediately after the training and 3 months after completing the trainingThe Short Form Health Survey to evaluate different dimensions of health related quality of life including mobility, emotional well-being, and cognitive impairment.
Changes in gait speedAt baseline, immediately after the training and 3 months after completing the training.gait speed will be evaluated under two conditions each over 1 minute: i) walking at comfortable speed, ii) walking while performing a cognitive task (dual task).
Changes in stride and swing time variabilityAt baseline, immediately after the training and 3 months after completing the training.Stride and swing time variability will be evaluated under two conditions each over 1 minute: i) walking at
Changes in cognitive function: number of digitsAt baseline, immediately after the training and 3 months after completing the trainingWorking memory (forward and backward digit span): Forward and backward digit span is a common measure of short-term memory (working memory). It is also a component of cognitive ability tests. Backward memory span is a more challenging variation which involves recalling items in reverse order.
Changes in cognitive function: number of correct / incorrect answersAt baseline, immediately after the training and 3 months after completing the trainingDual tasking (DT) walking performance: alternation in the ability to walk while simultaneously performing another task, have been related to gait and balance impairment. The negative effects of DT have been associated with an increased risk of falling, underscoring the clinical importance of DT abilities
Changes in functional mobility: score in Four Square Step TestAt baseline, immediately after the training and 3 months after completing the trainingFour Square Step Test is a dynamic balance test that clinically assesses the person's ability to step over objects forward, sideways, and backwards
Changes in stride lengthAt baseline, immediately after the training and 3 months after completing the training.Stride length will be evaluated under two conditions each over 1 minute: i) walking at
Changes in fear of fallingAt baseline, immediately after the training and 3 months after completing the trainingfalls Efficacy Scale International (FES-I).

Contacts

Primary ContactAnat Mirelman, PhD
anatmi@tlvmc.gov.il972-36974957
Backup ContactMoran Dorfman, MsPT
morando@tlvmc.gov.il972-36974957

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026