Comparison of Video Consent Versus Routine Consent for Participation in Research Studies
Completed · Not applicable
Conditions studied: Schizophrenia
In brief
The purpose of this study is to examine a novel technique for improving the informed consent process for participation in research by the older psychiatric population.
Key facts
- Study ID
- NCT00430391
- Run by
- University of California, San Diego
- People needed
- 382
- Starts
- 2003-12-01
- Expected to finish
- 2010-02-01
- Last updated by the study team
- 2013-06-19
Who can join
Age: 40 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- DSM-IV diagnosis of schizophrenia or no current or past major neuropsychiatric disorder (normal subjects)
- Fluency in English
- Written informed consent
You may not qualify if…
- Known or suspected dementia
Where it is running
- University of California, San Diego — San Diego, California, United States
Full record on ClinicalTrials.gov
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