Templates

The following ICD templates can be used and adapted to your study:

In capturing the details of your study into these templates, consult the glossary of lay terms for a large number of medical terms commonly used in research at website http://irb.ufl.edu/irb01/forms/glossary.html#G

ICD 1a - PARTICIPANT’S INFORMATION & INFORMED CONSENT DOCUMENT

ICD 1b - PARENTAL OR LEGAL GUARDIAN INFORMATION & INFORMED CONSENT

ICD 1c - INFORMATION AND ASSENT DOCUMENT FOR CHILDREN 7-18 YEARS

ICD 2a - PARTICIPANT’S INFORMATION LEAFLET & INFORMED CONSENT FOR ANONYMOUS QUESTIONNAIRES

ICD 2b - INFORMATION AND ASSENT DOCUMENT FOR CHILDREN 7-18 YEARS FOR ANONYMOUS QUESTIONNAIRE STUDY

ICD 2c - PARTICIPANT’S INFORMATION & INFORMED CONSENT DOCUMENT FOR A PARTICIPANT ADMINISTERED QUESTIONNAIRE

ICD 3a - PARTICIPANT’S INFORMATION & INFORMED CONSENT DOCUMENT FOR A MEDICATION TRIAL

ICD 3b - PARENTAL OR LEGAL GUARDIAN INFORMATION & INFORMED CONSENT DOCUMENT FOR A MEDICATION TRIAL

ICD 3c - INFORMATION AND ASSENT DOCUMENT FOR CHILDREN 7-18 YEARS FOR A MEDICATION TRIAL

ICD 4 - PARTICIPANT’S INFORMATION AND INFORMED CONSENT DOCUMENT FOR A FOCUS GROUP INTERVIEW RESEARCH STUDY

ICD 5 - PARTICIPANT’S INFORMATION & INFORMED CONSENT DOCUMENT FOR AN INDIVIDUAL IN-DEPTH INTERVIEW RESEARCH STUDY

ICD 6 - PARTICIPANT INFORMED CONSENT FOR HUMAN IMMUNODEFICIENCY VIRUS (HIV) TESTING

ICD 7 - CONSENT TO USE HEALTH RECORDS AND INFORMATION FOR A CASE STUDY

ICD 8 - PARTICIPANT INFORMATION AND INFORMED CONSENT FORM FOR RESEARCH INVOLVING GENETIC STUDIES

ICD 9a - PARTICIPANT’S INFORMATION & INFORMED CONSENT DOCUMENT FOR CRITICALLY ILL PATIENTS ADMITTED IN AN INTENSIVE CARE UNIT [ONCE A PATIENT HAS BECOME CAPABLE OF CONSENTING TO THE RESEARCH]

ICD 9b - INFORMATION & INFORMED CONSENT DOCUMENT FOR RELATIVES OF CRITICALLY ILL PATIENTS ADMITTED IN AN INTENSIVE CARE UNIT [ONCE A PATIENT HAS BECOME CAPABLE OF CONSENTING TO THE RESEARCH]

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