Ethical Considerations for Clinical Data Sharing in Craniofacial Research: Recommendations From a Multidisciplinary Working Group

ObjectiveTo propose recommendations for ethical, participant-centered clinical data sharing in craniofacial research.DesignSeries of deliberative multidisciplinary expert working group meetings to develop recommendations.SettingTwo 1-h virtual meetings; one all-day hybrid meeting.Patients, ParticipantsWorking group (<i>n</i> = 16) comprised individuals with expertise in craniofacial research, bioethics, and patient/caregiver advocacy, as well as lived experience of craniofacial conditions.InterventionsThe working group first reviewed prior empirical data about research participant attitudes about data sharing then drafted initial recommendations that were built on the data and the group's collective expertise. Recommendations were iteratively refined until the group agreed upon their final presentation.Main outcome measuresWorking group endorsement of recommendations.ResultsThe working group produced 16 recommendations that addressed considerations for primary and secondary researchers, data repositories, and the craniofacial research community across 5 domains. These domains address: (1) research team communication with participants, (2) data collection and protections, (3) data governance, (4) education for researchers, and (5) remaining research gaps. Recommendations highlight the importance of prioritizing the experiences of those with lived experience of craniofacial conditions in decision-making about data sharing, navigating varied perspectives on privacy protections for facial images, and striving to implement trustworthy data sharing and governance practices.ConclusionsThis summary of recommendations offers guidance for the craniofacial research community to advance participant-centered clinical data sharing practices. Ethical data sharing that accounts for participants' experiences and values has potential to advance scientific research and improve outcomes for individuals with craniofacial conditions, their families, and their communities.

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Publication Details

Journal
The Cleft Palate-Craniofacial Journal
Published
2025-12-02
DOI
https://doi.org/10.1177/10556656251398916
Primary Topic
Ethics in Clinical Research
Type
article
Field-Weighted Citation Impact
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article

Ethical Considerations for Clinical Data Sharing in Craniofacial Research: Recommendations From a Multidisciplinary Working Group

Stephanie M. Fullerton, Sara Kinter, Nicola Marie Stock, Kathleen R. Bogart et al.
The Cleft Palate-Craniofacial Journal
Ethics in Clinical Research
article

Ethical Considerations for Clinical Data Sharing in Craniofacial Research: Recommendations From a Multidisciplinary Working Group

Stephanie M. Fullerton, Sara Kinter, Nicola Marie Stock, Kathleen R. Bogart, Laura P. Stueckle, Melissa Tumblin, Canice E. Crerand, Stephanie A. Kraft, Kelly N. Evans, Christy M. McKinney, Alexis L. Johns, Carrie L. Heike, Amy Schefer, Erica Klauber, Amy Mendillo, Alexis Prepotente
article en

Abstract

ObjectiveTo propose recommendations for ethical, participant-centered clinical data sharing in craniofacial research.DesignSeries of deliberative multidisciplinary expert working group meetings to develop recommendations.SettingTwo 1-h virtual meetings; one all-day hybrid meeting.Patients, ParticipantsWorking group (<i>n</i> = 16) comprised individuals with expertise in craniofacial research, bioethics, and patient/caregiver advocacy, as well as lived experience of craniofacial conditions.InterventionsThe working group first reviewed prior empirical data about research participant attitudes about data sharing then drafted initial recommendations that were built on the data and the group's collective expertise. Recommendations were iteratively refined until the group agreed upon their final presentation.Main outcome measuresWorking group endorsement of recommendations.ResultsThe working group produced 16 recommendations that addressed considerations for primary and secondary researchers, data repositories, and the craniofacial research community across 5 domains. These domains address: (1) research team communication with participants, (2) data collection and protections, (3) data governance, (4) education for researchers, and (5) remaining research gaps. Recommendations highlight the importance of prioritizing the experiences of those with lived experience of craniofacial conditions in decision-making about data sharing, navigating varied perspectives on privacy protections for facial images, and striving to implement trustworthy data sharing and governance practices.ConclusionsThis summary of recommendations offers guidance for the craniofacial research community to advance participant-centered clinical data sharing practices. Ethical data sharing that accounts for participants' experiences and values has potential to advance scientific research and improve outcomes for individuals with craniofacial conditions, their families, and their communities.

The Cleft Palate-Craniofacial Journal
Oregon State University (US), Nationwide Children's Hospital (US), Children's Hospital of Los Angeles (US), University of the West of England (GB), University of Washington (US), Rainier Clinical Research Center (US), International Craniofacial Institute (US), Community Living (US), American Cleft Palate-Craniofacial Association (US), National Organization for Rare Disorders (US), The Ohio State University (US)
Openalex Percentile: Top 52%
Ethics in Clinical Research
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