Educational intervention study on effectiveness of novel simulation model for upper gastrointestinal endoscopic hemostasis

Educational intervention study on effectiveness of novel simulation model for upper gastrointestinal endoscopic hemostasis - Educational intervention study on effectiveness of novel simulation model for upper gastrointestinal endoscopic hemostasis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000035735

Enrollment

Registered

2019-02-01

Start date

2019-01-31

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal bleeding

Interventions

Investigator will take informed consent from participants by oral agreement. Then participants will complete the questionnaires both before and after simulation training. Training for endoscopic hemos

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Gastroenterological doctor or resident doctor who is belonging to McMaster University, Tohoku University, or related hospitals of Tohoku University.

Exclusion criteria

Exclusion criteria: Exclusion criteria will be the trainees who cannot speak English in Canada,and who cannot speak Japanese in Japan.

Design outcomes

Primary

Measure	Time frame
To evaluate effectiveness of the novel simulation model for endoscopic trainee.	—

Secondary

Measure	Time frame
To clarify factors associated with difficulty of upper gastrointestinal endoscopic hemostasis.	—

Countries

Japan,North America

Contacts

Public ContactTakeshi Kanno

Tohoku University graduate school of Medicine Division of Gastroenterology

kanno.takeshi@med.tohoku.ac.jp022-717-7171

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026