The COPE-Trial—Communicating prognosis to parents in the neonatal ICU: Optimistic vs. PEssimistic : study protocol for a randomized controlled crossover trial using two different scripted video vignettes to explore communication preferences of parents of preterm infants

dc.contributor.authorForth, Fiona A.
dc.contributor.authorHammerle, Florian
dc.contributor.authorKönig, Jochem
dc.contributor.authorUrschitz, Michael S.
dc.contributor.authorNeuweiler, Philipp
dc.contributor.authorMildenberger, Eva
dc.contributor.authorKidszun, André
dc.date.accessioned2022-08-22T10:18:19Z
dc.date.available2022-08-22T10:18:19Z
dc.date.issued2021
dc.description.abstractBackground One of the numerous challenges preterm birth poses for parents and physicians is prognostic disclosure. Prognoses are based on scientific evidence and medical experience. They are subject to individual assessment and will generally remain uncertain with regard to the individual. This can result in differences in prognostic framing and thus affect the recipients’ perception. In neonatology, data on the effects of prognostic framing are scarce. In particular, it is unclear whether parents prefer a more optimistic or a more pessimistic prognostic framing. Objective To explore parents’ preferences concerning prognostic framing and its effects on parent-reported outcomes and experiences. To identify predictors (demographic, psychological) of parents’ communication preferences. Design, setting, participants Unblinded, randomized controlled crossover trial (RCT) at the Division of Neonatology of the University Medical Center Mainz, Germany, including German-speaking parents or guardians of infants born preterm between 2010 and 2019 with a birth weight < 1500 g. Inclusion of up to 204 families is planned, with possible revision according to a blinded sample size reassessment. Intervention Embedded in an online survey and in pre-specified order, participants will watch two video vignettes depicting a more optimistic vs. a more pessimistic framing in prognostic disclosure to parents of a preterm infant. Apart from prognostic framing, all other aspects of physician-parent communication are standardized in both videos. Main outcomes and measures At baseline and after each video, participants complete a two-part online questionnaire (baseline and post-intervention). Primary outcome is the preference for either a more optimistic or a more pessimistic prognostic framing. Secondary outcomes include changes in state-anxiety (STAI-SKD), satisfaction with prognostic framing, evaluation of prognosis, future optimism and hope, preparedness for shared decision-making (each assessed using customized questions), and general impression (customized question), professionalism (adapted from GMC Patient Questionnaire) and compassion (Physician Compassion Questionnaire) of the consulting physician. Discussion This RCT will explore parents’ preferences concerning prognostic framing and its effects on physician-parent communication. Results may contribute to a better understanding of parental needs in prognostic disclosure and will be instrumental for a broad audience of clinicians, scientists, and ethicists.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-7590
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7604
dc.language.isoengde
dc.rightsCC-BY-4.0*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleThe COPE-Trial—Communicating prognosis to parents in the neonatal ICU: Optimistic vs. PEssimistic : study protocol for a randomized controlled crossover trial using two different scripted video vignettes to explore communication preferences of parents of preterm infantsen_GB
dc.typeZeitschriftenaufsatzde
jgu.journal.titleTrialsde
jgu.journal.volume22de
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternative884de
jgu.publisher.doi10.1186/s13063-021-05796-3de
jgu.publisher.issn1745-6215de
jgu.publisher.nameBioMed Centralde
jgu.publisher.placeLondonde
jgu.publisher.year2021
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610de
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde

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