Trial record 3 of 31 for:    sleep | NICHD

Improving the Self-Efficacy of African American Parents in Infant Supine Sleep (PrAAIS)

This study is currently recruiting participants.
Verified October 2012 by University of Michigan
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Dr. Kathryn Moseley, University of Michigan
ClinicalTrials.gov Identifier:
NCT01707173
First received: October 11, 2012
Last updated: October 19, 2012
Last verified: October 2012
  Purpose

This is a research study of African American parents/caregivers of newborns. The purpose of this research study is to learn what type of educational materials about infant safety and safe infant sleep are most effective and acceptable to parents and caregivers. The investigators will compare the responses of parents who receive enhanced materials to the responses of parents who receive the ordinary materials that are currently in use.


Condition Intervention
Infant Supine Sleep
Other: Tailored educational materials
Other: Standard sleep educational materials

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Official Title: Improving the Self-Efficacy of African American Parents in Infant Supine Sleep

Resource links provided by NLM:


Further study details as provided by University of Michigan:

Arms Assigned Interventions
Standard educational materials Other: Standard sleep educational materials
Experimental: Tailored educational materials
Parents/caregivers will received educational materials tailored to their specific beliefs and barriers about infant supine sleep along with a DVD detailing standard guidelines along with specific solutions and facilitators to infant supine sleep.
Other: Tailored educational materials

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:-

- Self-identified AA adult parents and primary caregivers (≥ 18 years of age) of newborns ≤ four weeks old at the time of the infant's first office visit to the pediatrician.

Exclusion Criteria:

  • Foster parents and temporary guardians:
  • Prior study participants:
  • Parents without a reliable phone number:
  • Parents without ready access to a DVD player: an ownership of a DVD player,
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01707173

Contacts
Contact: Jamie I Perryman, PhD 734-615-6440 pjamie@med.umich.edu
Contact: Kathryn L Moseley, MD 734-615-3139 klmosele@med.umich.edu

Locations
United States, Michigan
Child Health Evaluation and Research Unit, University of Michigan Recruiting
Ann Arbor, Michigan, United States, 48109-0456
Contact: Jamie I Perryman, PhD    734-615-6440    pjamie@med.umich.edu   
Contact: Kathryn L Moseley, MD    734-615-3539    klmosele@med.umich.edu   
Sponsors and Collaborators
University of Michigan
  More Information

No publications provided

Responsible Party: Dr. Kathryn Moseley, Assistant Professor, University of Michigan
ClinicalTrials.gov Identifier: NCT01707173     History of Changes
Other Study ID Numbers: 1 RO1 HD064770-01A1, HUM00048679
Study First Received: October 11, 2012
Last Updated: October 19, 2012
Health Authority: United States: Institutional Review Board
United States: Federal Government

Keywords provided by University of Michigan:
SIDS

ClinicalTrials.gov processed this record on April 17, 2014