Clinical trials tutorials
Mother-newborn pairs serum would be collected to measure cortisol. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies. Try the modernized ClinicalTrials.
Learn more about the modernization effort. Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or results information. Search for terms. Save this study. Warning You have reached the maximum number of saved studies Listing a study does not mean it has been evaluated by the U. Federal Government. Read our disclaimer for details. Recruitment status was: Not yet recruiting First Posted : March 29, Last Update Posted : April 3, Study Description.
The present study aimed to determine whether infants disorders of regulation of states are associated with perinatal anxiety, and further to explore the efficacy of the behavioral intervention in enhancing positive interactions between mothers and their infants and thus ameliorating infants' disorders of regulation of states. Detailed Description:. The subjects were recruited from the hospitalized pregnant women waiting for delivery from the department of gynecology and obstetrics of the first affiliated hospital of Xi'an Jiaotong university.
A total of perinatal anxiety women were divided to two group behavioral intervention group and control group according to mental health assessment. The following example study records and study papers are fictional and were created to illustrate key concepts for results data entry in PRS.
Each document below is provided as a PDF file. Try the modernized ClinicalTrials. Learn more about the modernization effort. Hide glossary Glossary Study record managers: refer to the Data Element Definitions if submitting registration or results information. Search for terms. Related Pages Login to ClinicalTrials. National Library of Medicine U. She and her staff are responsible for the negotiation of clinical trials for the University. She has been involved in the creation of two clinical trials offices and works closely with the newly established Center for Clinical Investigation at Yale.
She has spoken frequently at NCURA meetings on the subject of clinical trials and clinical trial negotiation. In addition to an undergraduate education in biology and nursing she holds a master's degree in health administration from NYU. Ed has had extensive pre and post award experience. Ed is the immediate past treasurer of the National Council of University Research Administrators, a past Board member, has been on many committees, and has held many offices at the regional level.
Ed has presented at the regional level on contract negotiation and how to appropriately budget for a clinical trial at many NCURA regional and annual meetings. He also was a faculty member on three NCURA live video workshops on topics ranging from pre and post award essentials, departmental research administration to current post award issues.
In this role, she serves as a senior administrative officer of the University responsible for non-financial aspects of sponsored programs administration, including the development and implementation of research policies and processes. Gunta serves on numerous University of Rochester standing committees such as the conflict of interest committee, technology transfer policy committee, institutional biosafety committee, and radiation safety committee.
One of her key responsibilities is the development of conflict of interest plans and strategies for clinical researchers.
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