NCT06435078

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2017

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 6, 2017

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 21, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 21, 2017

Completed
6.8 years until next milestone

First Submitted

Initial submission to the registry

May 22, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

May 30, 2024

Completed
Last Updated

May 31, 2024

Status Verified

May 1, 2024

Enrollment Period

6 months

First QC Date

May 22, 2024

Last Update Submit

May 29, 2024

Conditions

Keywords

Pressing Evaluation and Training SystemVirtual RealityAugmented Reality

Outcome Measures

Primary Outcomes (1)

  • Force-track testing

    Subjects will be asked to track the target force and presses task digit to fit the target line until finish.

    Before and after intervention (4 weeks)

Secondary Outcomes (2)

  • Sequential testing( reaction time)

    Before and after intervention (4 weeks)

  • Sequential testing( correct ratio )

    Before and after intervention (4 weeks)

Study Arms (2)

AR-mPETS

EXPERIMENTAL

subjects will be instructed to execute simulated piano playing tasks with Augmented Reality.

Device: mPETS(modified-PETS system)

VR-mPETS

ACTIVE COMPARATOR

subjects will be instructed to execute simulated piano playing tasks with Virtual Reality.

Device: mPETS(modified-PETS system)

Interventions

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.

AR-mPETSVR-mPETS

Eligibility Criteria

Age20 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Aged ≥ 65
  • Healthy adult (no skeletal muscle, neurological disease that will affect training).

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Cheng Kung University

Tainan, 701, Taiwan

Location

Related Publications (53)

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    BACKGROUND
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MeSH Terms

Conditions

Alzheimer Disease

Condition Hierarchy (Ancestors)

DementiaBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesTauopathiesNeurodegenerative DiseasesNeurocognitive DisordersMental Disorders

Study Officials

  • Fong-Chin Su

    Chair Professor

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chair Professor

Study Record Dates

First Submitted

May 22, 2024

First Posted

May 30, 2024

Study Start

March 6, 2017

Primary Completion

August 21, 2017

Study Completion

August 21, 2017

Last Updated

May 31, 2024

Record last verified: 2024-05

Locations