Education & Training
Research Study Participation Consent
Research study participation consent form with IRB-style informed consent provisions. 1 signer (participant).
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# Research Study Participation Consent **Date:** ___________ This Research Study Participation Consent ("Consent") is submitted by: **Participant:** ___________ ("Participant") ## 1. Study Information **Study Title:** ___________ **Principal Investigator:** ___________ **Research Institution/Organization:** ___________ **IRB/Ethics Committee Approval Number:** ___________ **Sponsor (if applicable):** ___________ **Study Contact Phone:** ___________ **Study Contact Email:** ___________ ## 2. Purpose of the Study ___________ ## 3. Study Procedures **Study Type:** ___________ **Description of Procedures:** ___________ **Estimated Time Commitment:** ___________ **Number of Visits/Sessions:** ___________ **Study Duration:** ___________
Fields (32)
effective date
date 路 required
participant name
text 路 required
study title
text 路 required
principal investigator
text 路 required
institution
text 路 required
irb number
text
sponsor
text
study phone
text 路 required
study email
text 路 required
study purpose
textarea 路 required
study type
select 路 required
procedures
textarea 路 required
time commitment
select 路 required
num sessions
select 路 required
study duration
select 路 required
risk level
select 路 required
risks
textarea 路 required
risk mitigation
textarea 路 required
participant benefits
select 路 required
society benefits
textarea 路 required
compensation
select 路 required
compensation details
text
prorated
select 路 required
data identifiability
select 路 required
data storage
select 路 required
data retention
select 路 required
data sharing
select 路 required
irb contact
text
irb phone
text
future contact
select 路 required
governing state
select 路 required
participant signer name
text 路 required
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