Exploring the Effect of Visual Feedback on Motion Trajectory in a Virtual Reality Environment.
NCT ID: NCT04103957
Last Updated: 2021-05-26
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
60 participants
OBSERVATIONAL
2020-04-10
2021-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of Virtual Reality Multisensory Cooperative Task-Oriented Mirror Therapy
NCT07139379
Effects of Upper Extremity Rehabilitation Robot and Transcranial Direct Current Stimulation Among Patients With Stroke
NCT04055597
Effectiveness of IVR Combined With Task-Specific Training on Hemiplegic Arm Function Following Stroke
NCT05728866
Mixed Reality and Virtual Reality Technology With Mirror Therapy for Stroke Rehabilitation
NCT05903235
Effectiveness of Interactive Augmented Reality and Electrical Neuromodulation System in Persons With Stroke
NCT04003571
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Stroke onset time \> 1 week, and neurological status and medical condition are stable.
3. Brunnstrom stage III to V.
4. Can follow order.
1. Age:20\~100y/o.
2. No pain to affect upper extremities movement.
Exclusion Criteria
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.
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.
20 Years
100 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Taiwan University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Tzu Ling Tai, MAMS
Role: PRINCIPAL_INVESTIGATOR
National Taiwan University Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
National Taiwan University Hospital
Taipei, Zhongzheng Dist, Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
201907130RINB
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.