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Literature DB >> 18512655

Clinical research in low-literacy populations: using teach-back to assess comprehension of informed consent and privacy information.

Sunil Kripalani¹, Rachel Bengtzen, Laura E Henderson, Terry A Jacobson.

Abstract

Mesh：

Year: 2008 PMID： 18512655

Source DB: PubMed Journal: IRB ISSN： 0193-7758

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50 in total

1. A new look at informed consent for cancer clinical trials.

Authors: Allison R Baer; Marge Good; Lidia Schapira
Journal: J Oncol Pract Date: 2011-07 Impact factor: 3.840

Review 2. Improving the informed consent process for research subjects with low literacy: a systematic review.

Authors: Leonardo Tamariz; Ana Palacio; Mauricio Robert; Erin N Marcus
Journal: J Gen Intern Med Date: 2012-07-11 Impact factor: 5.128

Review 3. Assessing readability of patient education materials: current role in orthopaedics.

Authors: Sameer Badarudeen; Sanjeev Sabharwal
Journal: Clin Orthop Relat Res Date: 2010-10 Impact factor: 4.176

4. Sickle cell carriers' unmet information needs: Beyond knowing trait status.

Authors: Tilicia L Mayo-Gamble; David Schlundt; Jennifer Cunningham-Erves; Velma McBride Murry; Kemberlee Bonnet; Delores Quasie-Woode; Charles P Mouton
Journal: J Genet Couns Date: 2019-04-10 Impact factor: 2.537

5. Use of mobile devices and the internet for multimedia informed consent delivery and data entry in a pediatric asthma trial: Study design and rationale.

Authors: Kathryn Blake; Janet T Holbrook; Holly Antal; David Shade; H Timothy Bunnell; Suzanne M McCahan; Robert A Wise; Chris Pennington; Paul Garfinkel; Tim Wysocki
Journal: Contemp Clin Trials Date: 2015-04-03 Impact factor: 2.226

Clinical research in low-literacy populations: using teach-back to assess comprehension of informed consent and privacy information.

1. A new look at informed consent for cancer clinical trials.

Review 2. Improving the informed consent process for research subjects with low literacy: a systematic review.

Review 3. Assessing readability of patient education materials: current role in orthopaedics.

4. Sickle cell carriers' unmet information needs: Beyond knowing trait status.

5. Use of mobile devices and the internet for multimedia informed consent delivery and data entry in a pediatric asthma trial: Study design and rationale.

6. Length and complexity of US and international HIV consent forms from federal HIV network trials.

7. Effect of Health Literacy on Research Follow-Up.

8. Seeing Beyond the Margins: Challenges to Informed Inclusion of Vulnerable Populations in Research.

9. "Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.

10. "Teach-to-Goal" to Better Assess Informed Consent Comprehension among Incarcerated Clinical Research Participants.