Factors Influencing Parental Willingness to Consent to a Survey Study for Patients in the Pediatric Emergency Department

Author:

Fischer Kayleigh1,Smith Gabriella B.2,Luna Sofia E.3,Jamro-Comer Erica4,Leupold Olivia2,Ahmed Hamza5,Govindji Shiv6,Ahmad Fahd7

Affiliation:

1. Department of Emergency Medicine, McGovern Medical School, Houston, TX

2. Department of Biology, Washington University in St. Louis, St. Louis, MO

3. Stanford University School of Medicine, Stanford, CA

4. Department of Biostatistics, Washington University School of Medicine, St Louis, MO

5. NYU Grossman School of Medicine, New York, NY

6. University of Texas Rio Grande Valley School of Medicine, Edinburg, TX

7. Department of Pediatrics, Washington University School of Medicine, St Louis, MO.

Abstract

Objective To identify factors that impact parental willingness to consent to research studies conducted for their children during visits to pediatric emergency departments (EDs). Methods Parents and guardians of children receiving care in our pediatric ED were approached and asked if they would be willing to let their child participate in a research study requiring the child to complete an electronic questionnaire. No such questionnaire existed, however, because the primary purpose was to ascertain the parent's willingness to let their child participate. All parents were debriefed and informed of the true purpose of the study and asked to complete a survey themselves to help understand factors that influenced their initial decision of whether to consent. Bivariate tests and logistic regression were used to evaluate unadjusted and adjusted associations between parent and patient characteristics and parental consent decision. Results We approached 431 eligible parents about the hypothetical research study involving their children, and 386 (89.6%) consented for their children to participate. After the debriefing, 392 (91.0%) parents consented to complete the parental survey. We observed statistically significant associations between shorter length of ED stay to approach for consent for the study (P = 0.048) as well as longer travel time (P = 0.03) and willingness to consent in bivariate analysis, though this did not hold in regression analysis. Regression analysis revealed parents of children who have previously participated in research had 79 times lower odds of consenting to participate in our study adjusted for parent race, ethnicity, actual and perceived length of stay, travel time to the ED, and altruism. Conclusions A high proportion of parents consented to their child participating in research in our ED with previous child participation in research being associated with lower odds of parental consent even when adjusted for other factors. Our findings may inform future research practices and studies investigating parental perceptions and motivations surrounding research studies.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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