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

An Open-label, Randomized-controlled Trial of SIDCER Informed Consent Form and Conventional Informed Consent Form in Understanding of Normal Volunteers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20140727001
Enrollment
Unknown
Registered
2014-07-27
Start date
2014-07-27
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

No health&#45

Interventions

It is a new informed consent form.,It is a conventional informed consent form.
Experimental Other,Active Comparator Other
SIDCER ICF,Conventional ICF

Sponsors

Faculty of Medicine, Chiang Mai University
Lead Sponsor
Institute of Tropical Medicine&#44
Collaborator
Nagasaki University
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
The proportion of study participants who have post-test score of ≥80% After reading a given ICF Post-test questionnaire—

Secondary

MeasureTime frame
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—

Countries

Thailand

Contacts

Public ContactNutthiya Hanprasertpong

Faculty of Medicine, Chiang Mai University

knutthiya@gmail.com053-945353

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026