Clinical Trials Directory

Trials / Completed

CompletedNCT03306004

Neonatal Jaundice: Knowledge, Attitudes and Practices of Mothers and Medical Trainees and Providers in and Around Ogbomosho

Status
Completed
Phase
Study type
Observational
Enrollment
360 (actual)
Sponsor
University of Minnesota · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERQuestionare

Timeline

Start date
2016-11-01
Primary completion
2017-12-31
Completion
2017-12-31
First posted
2017-10-10
Last updated
2018-02-13

Locations

1 site across 1 country: Nigeria

Source: ClinicalTrials.gov record NCT03306004. Inclusion in this directory is not an endorsement.