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.
RECRUITING
NA
250 participants
INTERVENTIONAL
2026-02-01
2026-11-30
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.
Staff Experiences in Robotic Theatres
NCT03453736
Chatbot Effectiveness for Improving Mental Health and Reducing Stress in Nursing Students
NCT06542068
Effectiveness and Mechanisms of Lifestyle Intervention for College Students
NCT06239597
Assessing the Team SA Instrument in Measuring the Effectiveness of Communication Across Disciplines During ICU Rounds
NCT01856608
Influence of Different Teaching Strategies on the Academic Performance and Caring of Nursing Students
NCT05543538
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.
RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
experimental group
robot backend design and control training
robot training
robot backend design and control training
control group
Traditional class (not-robot )
control group
Traditional class (not-robot )
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
robot training
robot backend design and control training
control group
Traditional class (not-robot )
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Central Taiwan University of Science and Technology
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Chiu Shu-Ching
assistant professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Shu Ching Chiu
Role: PRINCIPAL_INVESTIGATOR
Central Taiwan University of Science and Technology
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Central Taiwan University of Science and Technology
Taichung, , 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.
2510300001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.