Use of Virtual Reality for the Assessment of Attentional and Reaction Abilities for Fall Risk Evaluation

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age60+
SponsorI.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio

About this trial

Aging is a condition characterized by a general decline in physical and cognitive performance, however its effects on various functions are still controversial. These changes lead to an increased risk of injuries, particularly due to falls. According to the World Health Organization (WHO) report, 28-35% of individuals aged over 65 experience a fall each year, and this percentage increases with age. For this reason, preventing falls among the elderly is undeniably one of the most critical public health issues in today's aging society. Nowadays, it is widely demonstrated that the loss of muscle strength and mass, along with decreased balance, significantly increases the risk of falls. However, with aging, numerous other changes occur that contribute to an increased risk of falls, such as a decline in cognitive function, including attention, reaction capabilities and memory, as well as other factors that worsen the quality of life, such as insufficient sleep or nutrition. According to WHO estimates, by 2030, the number of injuries due to falls will double. Therefore, it is of great importance to understand and analyze the factors contributing to falls among older adults in everyday life. For this reason, the principal aim of this study was to evaluate the correlation between the fall index and the Visual Attention, Reaction Time and visual field using the technologies of Virtual Reality (VR). Since aging brigs changes in different aspect, the secondary objectives aim to study the correlation also with i) sleep quantity and quality parameters, ii) risk of malnutrition, and iii) physical condition, muscle conditions and strength in order to have a comprehensive understanding of the factors that most contribute to the risk of falls. In addition to these objectives, the correlation between acute sleep deprivation and the risk of falls will also be analyzed, in order to understand how inadequate sleep quantity can impact injuries in the elderly.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Male or female, of any ethnicity;

Age ≥ 60 years;

Cognitively intact;

Autonomous ambulation;

Disqualifiers

Body Mass Index > 40.0;

History of epileptic episodes;

Bone fractures in the last 6 months;

Previous surgical treatments for orthopedic conditions performed in the six months prior to study inclusion;

Trial population

A minimum of 100 subjects aged 60 years or older will be recruited, but recruitment will continue until enough subjects are identified to reach the predetermined number for the second study. The subjects are chosen on the basis of the following inclusion and exclusion criteria

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

30 - second chair stand test

to assess the leg strength and endurance in older adults. Being in a specific sitting position on a chair, the test consists of getting up and sitting down as many times as possible in 30 seconds

Time frame
10 days ± 3 days after the familiarization day

Secondary outcomes

1

Virtual reality (VR-Brain Tracker)

Evaluation to assess visual attention through the Multiple Object Tracking paradigm.

Time frame
10 days ± 3 days after the familiarization day
2

Strength asessment

Handgrip Test (Kg) Flexors and Extensors of thigh muscles (Kg)

Time frame
10 days ± 3 days after the familiarization day
3

Balance test

balance assessment is conducted using Baiobit equipment from BTS Bioengineering. The maximal balance time in monopodalic will be considered (s)

Time frame
10 days ± 3 days after the familiarization day
4

Sleep assessment

Objective assessment of sleep quantity and quality using the MotionWatch 8® (CamTec, USA), and sleep diary.

Time frame
sleep monitoring duration: 10 days ± 3 days after the familiarization day

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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