Comparison of SIDCER informed consent and conventional informed consent in understanding of potential participants of clinical trials at Phramongkutklao hospital

Not Applicable

Completed

• Conditions: o health- related condition; informed consent; research ethics

• Registration Number: TCTR20140930001
• Lead Sponsor: Phramongkutklao hospital, Bangkok, Thailand

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-09-30
• Study Completion: 2016-09-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 550

Inclusion Criteria

A potential participant who is invited to take part in recruited clinical trials at Phramongkutklao hospital.

Exclusion Criteria

A subject who refuses to take part in the informed consent process along with the procedure of understanding evaluation by the post-test questionnaire; or a subject who cannot read and write Thai.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The proportion of study participants who have post-test score of ≥80% None Post-test questionnaire

Secondary Outcome Measures

Name	Time	Method
The total score of post-test None Post-test questionnaire,Score of each category of elements required None Post-test questionnaire,Time spent for all processes None Post-test questionnaire