Viewing Study NCT03306004


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Study NCT ID: NCT03306004
Status: COMPLETED
Last Update Posted: 2018-02-13
First Post: 2017-09-01
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Neonatal Jaundice: Knowledge, Attitudes and Practices of Mothers and Medical Trainees and Providers in and Around Ogbomosho
Sponsor: University of Minnesota
Organization:

Study Overview

Official Title: Neonatal Jaundice: Knowledge, Attitudes and Practices of Mothers and Medical Trainees and Providers in and Around Ogbomosho
Status: COMPLETED
Status Verified Date: 2018-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: 4NNJ
Brief Summary: Determine the knowledge attitude and practices of all levels of health care providers about neonatal jaundice
Detailed Description: During the routine post-natal visit, trained research personnel will inform the mother of the infant or medical practitioner that a study in being carried out to better understand the knowledge, attitudes and practices of mothers and health care providers for neonatal jaundice. The investigators will then proceed to ask the mothers or health care professionals if they would be interested in filling out an anonymous survey that will assess their knowledge of neonatal jaundice and their practices, if any, in caring for this condition. No PHI will be included and no written consent will be obtained as the written consent would be the only link to the person participating in the survey. Verbal consent will be obtained and we will explain that their medical care and care of the children will in no way be affected by their answers to the survey. We will carefully explain that their participation in the survey is voluntary.

For medical students, they will be informed that a study is being carried out to better understand the knowledge, attitudes and practices of medical trainees for neonatal jaundice. They will then be asked if they would be interested in filling out an anonymous survey that assess their knowledge of neonatal jaundice, and their practices, if any, in caring for this condition. No PHI will be included and no written consent will be obtained, as the written consent would be the only link to the person participating in the survey. Verbal consent will be obtained and we will explain that their academic standing will not be affected by their answers to the survey. We will carefully explain that their participation in the survey is voluntary.

All surveys will contain the names and contact information of the investigators.

The survey will be administered under the direction of the researchers by the researchers and/or their trained research team.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: