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:
University of Michigan
Collaborator:
National Institutes of Health: National Institute of Child Health and Human Development
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
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
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
National Institutes of Health: National Institute of Child Health and Human Development
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 May 21, 2013