Reading Level and Length of Written Research Consent Forms

Author:

Larson Elaine1,Foe Gabriella2,Lally Rachel3

Affiliation:

1. School of Nursing, Mailman School of Public Health, Columbia University; New York New York USA

2. School of Continuing Studies, Columbia University; New York New York USA

3. Human Research Protection Office, Columbia University; New York New York USA

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference6 articles.

1. Participant comprehension of research for which they volunteer: a systematic review;Montalvo;J Nurs Scholarship,2014

2. Giving consent without getting informed: a cross-cultural issue in research ethics;Ghandour;J Empir Res Hum Res Ethics,2013

3. How IRBs view and make decisions about consent forms;Klitzman;J Empir Res Hum Res Ethics,2013

4. Readability of consent form templates: a second look;Paasche-Orlow;IRB.,2013

5. Readability standards for informed-consent forms as compared with actual readability;Paasche-Orlow;N Engl J Med.,2003

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