We are interviewing primary care providers to get their thoughts on how best to provide care to patients with eating disorders.

We are hoping to have patient who under went doulbe-jaw surgery for obstructive sleep apnea fill out a survey to inform of us there experience, expectations, and results after surgery.

This project is studying the effect of pediatric care coordination on the behavioral health of children and parents.

Systematic reviews (SRs) of healthcare interventions should identify patient safety concerns; however, many SRs are designed to assess benefits, and preliminary evidence suggests that conclusions about harms in SRs might not be trustworthy. Using >19,000 SRs of drugs for which we have full texts (including >4,000 overlapping reviews), and using innovative methods for analysis (e.g., natural language processing), we will examine whether information about safety in SRs is consistent, whether SRs address safety concerns identified using real-world evidence, and whether SRs are consistent with safety information on drug labels. Based on best evidence, including findings from this study, we will develop contemporary guidance for synthesizing and reporting safety information in SRs.

To examine the effect of certain medications on the amount of placental DNA in the blood of pregnant women.

This Incubation Project is motivated by ethical questions around policies and practices concerning research engagement with U.S. Indigenous Peoples whose tribes are unrecognized by the federal government. The pilot study includes activities aimed at (1) elucidating their perspectives on environmental research ethics, (2) evaluating the breadth and depth of current environmental research engagements within their communities, and (3) assessing their perspectives and gathering feedback on emerging research policies.

The purpose of this study is to culturally adapt a mindfulness-based intervention for American Indian women.

The aim of this questionnaire is to explore awareness, perceptions and utilisations of PPI (Patient & Public Involvement) and the barriers to its use among researchers within the Psychiatric Genomics Research community. This survey is part of ongoing work from the Psychiatric Genomics Consortium (PGC) Outreach Committee and the International Society of Psychiatric Genetics (ISPG). Data will inform the PGC Outreach Committee on how it can support PGC members in their outreach activities and will be shared at a PGC World Wide Lab 2024/2025.

The purpose of the study is to identify certain processes following brain injury that may be associated with the risk of developing epilepsy.

The purpose of this study is to learn more about the long-term priorities of coastal community members.