Hao Wang
Chengdu, Sichuan, 610072, China
NCT Number: NCT07778186
This single-center randomized controlled trial will enroll 85 nuclear medicine undergraduate students. Participants will be randomized into two arms: a three-stage AI multi-interactive teaching intervention group (n=43) and a conventional lecture-based control group (n=42). The study is designed to compare theoretical knowledge, instructor-rated performance, student satisfaction, discussion participation, core concept comprehension, and classroom engagement between the two teaching approaches. Planned evaluations will be conducted after the teaching intervention.
Looking for future studies?
Notify Me18 year–25 year
All sexes
Interventional
Not applicable
Chengdu, Sichuan, 610072, China
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Undergraduate students receive nuclear medicine theoretical courses via AI-driven multiple interactive teaching mode.
Undergraduate students receive standard nuclear medicine theoretical courses by conventional lecture-based teaching.
Time frame: At the end of the teaching intervention (approximately 4-week teaching period)
Nuclear medicine theoretical knowledge post-test score; examination scale range from 0 (minimum, poorest performance) to 100 (maximum, best performance). Higher scores indicate better theoretical knowledge mastery. The between-group score difference will be compared.
Time frame: At the end of the teaching intervention (approximately 4-week teaching period)
Student classroom engagement is assessed using a validated classroom engagement rating scale. The total scale score ranges from 20 (minimum, poorest classroom engagement) to 100 (maximum, optimal classroom engagement). Higher scores represent better classroom engagement of students. The difference in post-intervention engagement scores between the two groups will be analyzed.
Time frame: At the end of the teaching intervention (approximately 4-week teaching period)
Student learning satisfaction is evaluated with a standardized learning satisfaction questionnaire. The overall questionnaire score ranges from 10 (minimum, lowest learning satisfaction) to 50 (maximum, highest learning satisfaction). Higher scores indicate higher student learning satisfaction with nuclear medicine teaching. Post-intervention satisfaction scores are compared between the AI-driven teaching group and the traditional lecture group.
Time frame: At the end of the teaching intervention (approximately 4-week teaching period)
Students' practical-relevant learning experience is assessed using a validated practical learning experience scale. The total scale score ranges from 15 (minimum, poorest practical learning experience) to 75 (maximum, optimal practical learning experience). Higher scores represent better practical learning experience and stronger perceived mastery of nuclear medicine practical knowledge. Post-intervention learning experience scores are compared between the AI-driven teaching group and the traditional lecture group.
Sichuan Provincial People's Hospital
Other
The Impact of AI-driven Multiple Interactive Teaching Model on Nuclear Medicine Students' Theoretical Knowledge and Practical Skills
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05207878
Healthy, Peripheral Nerve Injury Upper Limb
St Louis, Missouri, United States
View Trial DetailsNCT03876314
Alzheimer Disease, Behavior
Greensboro, North Carolina, United States
View Trial DetailsNCT07778472
Healthy, Pathological Conditions, Signs and Symptoms
West Palm Beach, Florida, United States
View Trial DetailsNCT06975319
Healthy, Immunisation Against Streptococcus Pneumoniae
Ghent, Belgium
View Trial Details