The Effect of Computerized Vestibular Function Assessment and Training System Combined With Cognitive/Motor Dual-task

Cognitive Decline Clinical Trial

Official title:

Investigating the Effect of Computerized Vestibular Function Assessment and Interactive Training System, Combined With Cognitive/Motor Dual-task for the Elderly With Dizziness

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT05990023
• Other study ID #: N202212070
• Status: Enrolling by invitation
• Phase: N/A
• Start date: November 1, 2023
• Est. completion date: May 14, 2026

Study information

• Verified date: May 2023
• Source: Taipei Medical University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to investigate the effect of computerized vestibular function assessment and interactive training system, combined with cognitive/motor dual-task for the elderly with dizziness. The investigators will compare the movement abilities among older adults with different cognitive level, and further establish an assessment module that can evaluate participants' dual-task performance in both vestibular and cognitive tasks. Finally, leveraging the advantages of sensor detection technology and computerized feedback, an appropriate dual-task rehabilitation approach for vestibular function and cognition will be developed.

Description:

Dizziness is one of the most common complaints among older adults and often a concern within healthcare systems. It leads to distressing sensations, reduced mobility, and decreased quality of life. Dizziness is also closely associated with falls, which are a major cause of comorbidities and mortality in older adults. During clinical rehabilitation training, it has been observed that some elderly patients with vestibular dizziness often experience difficulties with speech clarity, lack of attention, poor direction control, or easy forgetfulness of rehabilitation training content. Similar observations have been made by scholars who interacted with dizzy patients, noting difficulties in maintaining attention, deficits in attention and spatial memory, speech expression impairments, and impacts on spatial memory, fluency of speech, thinking abilities, calculation impairments, and other forms of numerical cognition. Clinical studies have already noted the association between vestibular dysfunction and cognitive impairment. However, there is limited research that can clarify the intricacies and complexities of this issue. Currently, there is scarce knowledge regarding the relationship between the vestibular system and specific cognitive aspects, as well as its correlation with balance deficits. This study aims to investigate the effect of computerized vestibular function assessment and interactive training system, combined with cognitive/motor dual-task for the elderly with dizziness. Drawing from previous clinical rehabilitation experiences, a method for assessing vestibular function and balance performance will be designed to compare the movement differences among older adults with different cognitive performances. Subsequently, through scientific and objective motion capture analysis, a comprehensive assessment module will be established to evaluate the dual-task performance of participants in both vestibular and cognitive tasks. The performance differences attributed to cognition will be analyzed, and the correlation with vestibular function performance will be integrated to serve as a prescription reference for computer-assisted rehabilitation interventions. Finally, leveraging the advantages of sensor detection technology and computerized feedback, an appropriate dual-task rehabilitation approach for vestibular function and cognition will be developed. Methods: First year, the study will recruit 60 elderly people and integrate the use of inertial sensors and force plates with vestibular and balance tests to establish a vertigo assessment system for the elderly. In the second year, the subjects were divided into two groups: a control group of 25 healthy elderly people, and an experimental group of 25 elderly people who had experienced dizziness and falls in the past two years. Data were collected using a motion analysis system combined with a computerized assisted assessment. The main analysis is whether the experience of dizziness or fall affects the balance, vestibular and cognitive related activities. In the third year, 40 vestibular hypofunction patients will be randomized into either traditional or dual-task group. Both groups will receive 2~3 times per week for 4 weeks of computerized vestibular interventions with and without dual-task training protocols. Expected achievements: Combining safe stochastic dual-task training and computer-assisted rehabilitation interventions in this 3-year project, the mechanisms of cognition related to vestibular training will be elucidated. The optimal strategy for vestibular rehabilitation can thus be established.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 150
• Est. completion date: May 14, 2026
• Est. primary completion date: February 14, 2026
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 55 Years to 85 Years

Eligibility

Inclusion Criteria:

• Year 1 (Study A):

1. Could walk more than 30 meters with or without walking aids independently.

2. Able to comprehend and communicate in Mandarin or Taiwanese.

3. Sufficient corrected vision that allows independent outdoor mobility.

• Year 2 (Study B):

1. Could walk more than 30 meters with or without walking aids independently.

2. Able to comprehend and communicate in Mandarin or Taiwanese.

3. Sufficient corrected vision that allows independent outdoor mobility.

4. Healthy participants and those who have experienced dizziness or falls within the past two years.

• Year 3 (Study C):

1. Could walk more than 30 meters with or without walking aids independently.

2. Able to comprehend and communicate in Mandarin or Taiwanese.

3. Sufficient corrected vision that allows independent outdoor mobility.

4. Willing to engage in moderate-intensity exercise for 45 minutes per session.

5. Participants who have experienced dizziness or falls within the past two years.

Exclusion Criteria:

• Year 1 (Study A):

1. Severe central or peripheral nervous system disorders.

2. Participants who are blind or deaf.

3. Individuals who cannot communicate or understand instructions.

4. Current fractures or significant joint injuries.

• Year 2 (Study B):

1. Severe central or peripheral nervous system disorders.

2. Participants who are blind or deaf.

3. Individuals who cannot communicate or understand instructions.

4. Current fractures or significant joint injuries.

• Year 3 (Study C):

1. Severe central or peripheral nervous system disorders.

2. Participants who are blind or deaf.

3. Individuals who cannot communicate or understand instructions.

4. Current fractures or significant joint injuries.

Related Conditions & MeSH terms

• Cognitive Decline
• Cognitive Dysfunction
• Dizziness
• Vertigo
• Vestibular Abnormality
• Vestibular Diseases
• Vestibular Function Disorder

Intervention

Other:
• Traditional vestibule rehabilitation training
Standing, using a gaze tracking system on a force plate to track a continuously moving target, with alerts when body sway exceeds a certain threshold. Standing, wearing an inertial sensor on the head and performing left-right or up-down head movements while maintaining gaze on a target, with a screen providing feedback on head movement speed. Standing, controlling body weight distribution on the force plate to reach a target position, with a screen displaying the current center of gravity position. Walking, synchronizing head movements with a rhythm or performing up-down head nods, with auditory cues indicating the desired head movement frequency. During continuous head rotations, stepping in a regular sequence of forward, backward, left, and right movements.
• Dual-task vestibule rehabilitation training
Adding a dual task of digit countdown and recitation to clinical balance training exercises. Incorporating a numerical calculation task into interactive screens during clinical balance training, with the participant's responses input by the researchers. Introducing upper limb exercises, such as button pressing or arm swinging, during clinical balance training. During continuous head rotations, following visual prompts on the display to perform forward, backward, left, and right displacements.

Locations

Country	Name	City	State
Taiwan	Taipei Medical University	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
Taipei Medical University

Country where clinical trial is conducted

Taiwan, 

References & Publications (29)

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* Note: There are 29 references in all — Click here to view all references

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rotation of head, chest, and pelvis.	Parameters from inertial sensors placed on the head, chest, and pelvis will be extracted. The parameters include rotational angles (degrees) of the head, chest, and waist.	3 year.
Primary	Inclination of head, chest, and pelvis.	Parameters from inertial sensors placed on the head, chest, and pelvis will be extracted. The parameters include angular velocities (degrees per second) of the head, chest, and waist.	3 year.
Primary	Acceleration of head, chest, and pelvis.	Parameters from inertial sensors placed on the head, chest, and pelvis will be extracted. The parameters include accelerations (meters per second squared) of the head, chest, and waist.	3 year.
Primary	Static Visual acuity.	Parameters recorded by a screen with optotype chart and eyeglass system.	3 year.
Primary	Dynamic Visual acuity.	Parameters recorded by a screen with optotype chart and eyeglass system during movements.	3 year.
Primary	Static vestibulo-ocular reflex (VOR gain)	The VOR gain calculated by dividing eye movement velocity by head rotation velocity. The eye movement velocity(degree per second) and head rotation velocity(degree per second) are recorded by a screen, eyeglass system, and inertial sensor on subject's head.	3 year.
Primary	Dynamic vestibulo-ocular reflex. (VOR gain)	The VOR gain calculated by dividing eye movement velocity by head rotation velocity. The eye movement velocity(degree per second) and head rotation velocity(degree per second) are recorded by a screen, eyeglass system, and inertial sensor on subject's head during movements.	3 year.
Primary	Step length (centimeter) during walking	Step length (centimeter) recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation from the starting location.	3 year.
Primary	Step frequency	Steps and times recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation from the starting location.	3 year.
Primary	Walking trajectory (centimeter)	The shift(centimeter) of light and motion markers on subjects recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation from the starting location.	3 year.
Primary	Step width (centimeter) during walking	The medial-lateral distance(centimeter) of light and motion markers on subject's feet recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation among the testing session.	3 year.
Primary	Step variability of step length (standard deviation) during walking	The standard deviation of step length(centimeter) among the testing session. The step length(centimeter) is recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation.	3 year.
Primary	Step variability of step width (standard deviation) during walking	The standard deviation of step width(centimeter) among the testing session. The step width(centimeter) is recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation.	3 year.
Primary	Speed (meter per second) during walking	Speed (meter per second) calculated by dividing walking distances by total walking times. The walking distances and times are recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation from the starting location.	3 year.
Primary	Lower limb Joint force (Newton)	Joint force is calculated by joint position(millimeter) and ground reaction force(Newton). The joint position(millimeter) is recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera), and ground reaction force(Newton) is recorded by forceplates.	3 year.
Primary	Lower limb Joint moment (Newton-metre)	Joint moment (Newton-metre) is calculated by multiplying ground reaction force(Newton) by limb length(meter). The limb length(meter) is recorded by meters or optical motion sensors(camera).	3 year.
Primary	Lower limb Joint power (Watt)	Joint Power(watt) is calculated as the "scalar product" of joint moment and joint angular velocity(degree per second). The joint angular velocity (degree per second) is recorded by wearable sensors (inertial movement units) or optical motion sensors (camera).	3 year.
Primary	Joint movement (degree)	Joint movement (degree) of subjects is recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) during flat ground walking and up/down stairs situation.	3 year.
Primary	Body center of mass sway (millimeter) during testing session	The shift (millimeter)) of light and motion markers on subject's pelvis recorded by wearable sensors (inertial movement unit) or optical motion sensors (camera) and forceplae during flat ground walking and up/down stairs situation.	3 year.
Secondary	Activities-Specific Balance Confidence Scale (ABC scale).	Clinical assessment scales to identify individuals with a fall risk. The minimum and maximum values are 0% and 100%, and whether higher scores mean a better outcome.	3 year.
Secondary	Dizziness Handicap Inventory (DHI).	Clinical assessment scales that quantifies the impact of dizziness on daily life. The minimum and maximum values are 0 and 100, and whether higher scores mean a worse outcome.	3 year.
Secondary	Hospital Anxiety and Depression Scale (HADS).	Clinical assessment scales to measure anxiety and depression in a general medical population of patients. The minimum and maximum values are 0 and 42, and whether higher scores mean a worse outcome.	3 year.
Secondary	Dynamic Gait Index (DGI).	Clinical assessment scales to test the ability of the participant to maintain walking balance while responding to different task demands, through various dynamic conditions. The minimum and maximum values are 0 and 24, and whether higher scores mean a better outcome.	3 year.
Secondary	Tinetti Fall Risk Assessment Tool (Tinetti Scale).	Clinical assessment scales to test the walking and balance ability to valuate the falling risk. The minimum and maximum values are 0 and 28, and whether higher scores mean a better outcome.	3 year.
Secondary	Montreal Cognitive Assessment Taiwanese version (MoCA).	Cognitive-related assessments. The minimum and maximum values are 0 and 30, and whether higher scores mean a better outcome. The minimum and maximum values are 0 and 24, and whether higher scores mean a better outcome.	3 year.
Secondary	Trail Making Test.	Clinical assessment scales which provide information about visual search speed, scanning, speed of processing, mental flexibility, and executive functioning. Longer time consumed means worse performance. An average score for TMT-A is 29 seconds and a deficient score is greater than 78 seconds. For TMT-B, an average score is 75 seconds and a deficient score is greater than 273 seconds.	3 year.
Secondary	Digit Span Test.	Clinical assessment scales to test subject's ability to remember a sequence of numbers that appear on the screen, one at a time. The minimum and maximum values are 0 and 21, and whether higher scores mean a better outcome.	3 year.
Secondary	Stroop Test.	Clinical assessment scales for color recognize.The minimum and maximum values are 1% and 100%, and whether the higher percentage rates mean better performance	3 year.