nderstanding of new informed consent form compared to conventional informed consent form among normal people

Not Applicable

Completed

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

• Registration Number: TCTR20140727001
• Lead Sponsor: Faculty of Medicine, Chiang Mai University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-07-27
• Study Completion: 2014-10-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

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

Inclusion Criteria

Normal volunteer aged 18 years old who can read and write Thai

Exclusion Criteria

Subject who does not have time approximately 0 5 to 1 hour for entirely reading a given ICF and doing a post test

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% After reading a given ICF Post-test questionnaire

Secondary Outcome Measures

Name	Time	Method
The total score of post-test After reading a given ICF Post-test questionnaire,Score of each category of elements required After reading a given ICF Post-test questionnaire,Time spent for all processes After reading a given ICF and doing a post-test questionnaire Post-test questionnaire