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Developments of Novel Virtual Visual and Haptic Stimulation Systems for the Elderly

Developments of Novel Virtual Visual and Haptic Stimulation Systems for the Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06435078
Enrollment
40
Registered
2024-05-30
Start date
2017-03-06
Completion date
2017-08-21
Last updated
2024-05-31

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

Conditions

Alzheimer Disease, Healthy Elderly

Keywords

Pressing Evaluation and Training System, Virtual Reality, Augmented Reality

Brief summary

previous studies indicated that sensory input can have positive impacts on finger force control in the elderly. Additionally, according to previous reports, apart from pharmacotherapy, nonpharmacologic interventions, such as psychosocial-environmental treatments, are emerging for the behavior and affective symptoms in AD . Moreover, enhanced finger force control and coordination lead to better hand dexterity and is believed to eventually improve life independence in the healthy elderly and the elderly with AD. Therefore, this study aims to develop novel virtual visual and haptic stimulation systems for the elderly to enhance their finger force control.

Interventions

DEVICEmPETS(modified-PETS system)

The pressing evaluation and training system (PETS) consists of five force transducers, a pad position-adjustable frame, and biofeedback system. Five force transducers are used to collect the applied normal force from five digits.

Sponsors

National Cheng-Kung University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

Healthy elderly Inclusion Criteria: * Aged ≥ 65 * Healthy adult (no skeletal muscle, neurological disease that will affect training).

Exclusion criteria

* Neurological disorders * Musculoskeletal problems * History of surgery Patients with Alzheimer's disease Inclusion Criteria: * Diagnosed with Alzheimer's disease. * No skeletal muscle, neurological disease that will affect training.

Design outcomes

Primary

MeasureTime frameDescription
Force-track testingBefore and after intervention (4 weeks)Subjects will be asked to track the target force and presses task digit to fit the target line until finish.

Secondary

MeasureTime frameDescription
Sequential testing( reaction time)Before and after intervention (4 weeks)In sequential testing, subjects will be asked to follow the pressing guide. The reaction time of sequential movements will be recorded and calculated.
Sequential testing( correct ratio )Before and after intervention (4 weeks)In sequential testing, subjects will be asked to follow the pressing guide. The correct ratio of sequential movements will be recorded and calculated.

Countries

Taiwan

Outcome results

None listed

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