Clinical Trials Logo

Clinical Trial Summary

To address the content, timing, efficacy, and impact of prenatal education about newborn screening generally and sample retention specifically.


Clinical Trial Description

It is widely recognized that new parents receive insufficient information about newborn screening (NBS) and little or no information regarding the retention of residual newborn screening samples. Our current research (R01 HD058854) clearly demonstrates that parents are supportive of NBS and the research use of residual specimens, but they want information before the child is born and want an informed choice regarding the retention and use of residual samples. Previous research has outlined the basic elements of what parents want to know about NBS generally. However, given that many states are adopting an "opt-out" approach for residual samples, it is unclear what basic information parents want to know to enable an informed choice about this practice. While it is recognized that retention and use of residual NBS samples is a valuable research resource, there are prevalent concerns in the NBS community that discussion of this will lead some parents to decline NBS altogether. Some authorities have suggested that discussions of NBS and residual sample retention be conducted separately to reduce the risk that parents will confuse the issues and decline NBS altogether.

To address this the project has the following specific aims:

Specific Aim 1) To determine what pregnant women, young mothers, and their partners want to know regarding the retention and use of residual bloodspot samples

Specific Aim 2) To create multimedia educational tools to be used in the prenatal care environment that will provide basic information about NBS and the core information determined through Specific Aim 1 about residual sample retention and use.

Specific Aim 3) To determine the impact of the prenatal education intervention on parental knowledge, attitudes, and decisions regarding NBS services and the retention and use of residual samples in diverse populations of English and Spanish speaking pregnant women.

Specific Aim 4) To examine the normative/ethical implications of the results of SA3 for the conduct of state NBS programs. Recommendations on the content and timing of parental NBS education will be developed. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


NCT number NCT02676245
Study type Interventional
Source University of Utah
Contact
Status Completed
Phase N/A
Start date September 2013
Completion date October 2014

See also
  Status Clinical Trial Phase
Not yet recruiting NCT06192511 - Implementing a Novel Consent Process for Biospecimen Research After Newborn Screening N/A
Recruiting NCT04393701 - A Pilot Study for Systematic Neonatal Screening for Lysosomal Storage Diseases Using Tandem Mass Spectrometry N/A
Completed NCT03141307 - The Effect of Electronic Informed Consent Information (EICI) on Residual Newborn Specimen Research N/A
Recruiting NCT06058910 - Bilistick Point-of-care System 2.0 Bilirubin Validation
Completed NCT02590328 - Neonatal Screening of Severe Combined Immunodeficiencies
Completed NCT02374281 - Autonomic Nervous System Reactivity of the Newborn After a Nociceptive Stress: Interest of Sucrose and Non-nutritive Sucking Phase 3
Completed NCT00865150 - Amino Acid and Acylcarnitine Profiles in Premature Neonates N/A