Exploring the Effect of Visual Feedback on Motion Trajectory in a Virtual Reality Environment.

Stroke Clinical Trial

Official title:

Exploring the Effect of Visual Feedback on Motion Trajectory in a Virtual Reality Environment.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04103957
• Other study ID #: 201907130RINB
• Status: Recruiting
• Start date: April 10, 2020
• Est. completion date: December 2021

Study information

• Verified date: May 2021
• Source: National Taiwan University Hospital
• Contact: Tzu Ling Tai, MAMS
• Phone: 02-23123456
• Email: tzulingtai[@]gmail.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The rehabilitation intensity and frequency of upper extremities of stroke patients is insufficient. Virtual reality technique may solved this problem. The investigators want to build up the motion trajectory system by head-mounted display virtual reality technique, and to explore the effect of visual feedback on motion trajectory in a virtual reality environment.

Description:

How to increase the rehabilitation intensity in the critical rehabilitation window for stroke patients (half year since onset) was very important. The training intensity and frequency of upper extremities is insufficient. The proprioceptive neuromuscular facilitation (PNF) movements of upper extremities are applied to all daily upper extremities movement. The goals of this study are that the investigators want to build up the motion trajectory system by head-mounted display virtual reality technique, and the investigators want to explore the effect of visual feedback on motion trajectory in a virtual reality environment. The investigators will record the motion patterns, motion trajectory and the deviation of position and angle comparing to the normal PNF movement pattern to analyze the motion accuracy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 2021
• Est. primary completion date: December 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 100 Years

Eligibility

Stroke patients Inclusion criteria

1. Age:20~100y/o.

2. Stroke onset time > 1 week, and neurological status and medical condition are stable.

3. Brunnstrom stage III to V.

4. Can follow order.

Exclusion criteria

1. Crucial organ failure, including heart, lung, liver, and kidney.

2. Brain operation and epilepsy.

3. Severe metal illness and aphasia, so cannot follow order

4. Feel uncomfortable while using virtual reality.

5. Crucial eye problems, including color-blind, weak color, cataract, glaucoma, etc.

6. Mental illness, neuro-musculoskeletal system lesions, vertigo, claustrophobic.

7. Illness and pain to affect upper extremities movement.

Healthy people Inclusion criteria

1. Age:20~100y/o.

2. No pain to affect upper extremities movement.

Exclusion criteria

1. Feel uncomfortable while using virtual reality.

2. Crucial eye problems, including color-blind, weak color, cataract, glaucoma, etc.

3. Cognition impairment, history of mental illness, neuro-musculoskeletal system lesions, vertigo, claustrophobic.

4. Epilepsy.

Related Conditions & MeSH terms

• Control
• Stroke

Locations

Country	Name	City	State
Taiwan	National Taiwan University Hospital	Taipei	Zhongzheng Dist

Sponsors (1)

Lead Sponsor	Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Motion accuracy	Record the motion patterns, motion trajectory and the deviation of position and angle comparing to the normal PNF movement pattern to analyze the motion accuracy	during the experiment