Readability of informed consent documents and its impact on consent refusal rate

Pharma studies performed better and ICDs have improved in their readability and ICMR guidelines compliance.

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Publication Details

Journal
Perspectives in Clinical Research
Published
2024-08-30
DOI
https://doi.org/10.4103/picr.picr_322_23
Citations
1
Primary Topic
Ethics in Clinical Research
Type
article
Field-Weighted Citation Impact
0.54
Controls
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article

Readability of informed consent documents and its impact on consent refusal rate

Ankita Kulkarni, Yashashri Shetty, Ishita C. Lanjewar, Yash V. Kamath
1 citations
Perspectives in Clinical Research
Ethics in Clinical Research
0.54
article

Readability of informed consent documents and its impact on consent refusal rate

Ankita Kulkarni, Yashashri Shetty, Ishita C. Lanjewar, Yash V. Kamath
article en
1 citations

Abstract

Pharma studies performed better and ICDs have improved in their readability and ICMR guidelines compliance.

Perspectives in Clinical ResearchVol. 16(1)
King Edward Memorial Hospital and Seth G.S. Medical College (IN)
Quality Education
Openalex Percentile: Top 29%
Ethics in Clinical Research
0.54
DOIOpen Access PDFOpenAlex
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