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Prevention of Shaken Baby Syndrome - Article


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Child Development


Clinical Trial: Prevention of Shaken Baby Syndrome

This study is currently recruiting patients.

Sponsored by: Harborview Injury Prevention and Research Center
Information provided by: Harborview Injury Prevention and Research Center

Purpose

This research project seeks to implement an early intervention program that can be effective in the prevention of Shaken Baby Syndrome (SBS) and infant abuse. Our hypothesis is that the Period of PURPLE Crying intervention program can reduce shaking and abuse of infants through changes in knowledge, attitudes and behaviors about early infant crying, especially inconsolable crying. In this 3-year project, we will implement and evaluate an intervention program in selected prenatal classes, hospitals, and primary care pediatric practices.

In this randomized, controlled trial, we will enroll a total of 3000 women/families who are about to give birth or have just given birth to a healthy infant. At each of the three sites (newborn nursery, pediatrician offices and prenatal classes), we will enroll 1000 subjects. Half of all subjects will receive intervention materials (a video, pamphlet and bib/burp cloth) about infant crying. The other half, the control group, will receive comparable materials on infant safety. All subjects will be asked to complete a brief questionnaire at the time of enrollment (pre test), review the materials they receive, complete the Baby’s Day Diary for 4 days when the infant is 5 weeks of age and complete a telephone questionnaire (post test) when the infant is 8 weeks of age.

Condition Treatment or Intervention
Child Abuse
Shaken Baby Syndrome
 Behavior: Education about infant crying

MedlinePlus related topics:  Child Abuse

Study Type: Interventional
Study Design: Prevention, Randomized, Single Blind, Active Control, Single Group Assignment, Efficacy Study

Official Title: Parents Helping Infants Study: Preventing Shaken Baby Syndrome and Child Abuse

Further Study Details: 
Primary Outcomes: Knowledge and attitudes about crying, shaking and abuse; Caregiver behavior; Parenting sense of competence; Maternal depression
Expected Total Enrollment:  3000

Study start: January 2005;  Expected completion: June 2007
Last follow-up: August 2006;  Data entry closure: September 2006

The specific goals of the program are: (1) To change the understanding (i.e., knowledge and attitudes) and reduce the frustration of parents of new infants about the normality of the frustrating properties of crying; (2) To change the behavior of parents to increase caregiving contact in response to crying but to ‘walk away’ if frustrated; (3) To provide parents with the ability to communicate to other caregivers (relatives, baby-sitters) the knowledge and behavior to reduce frustration induced by inconsolable crying; (4) To provide effective knowledge, skills and teaching materials to health care providers in direct contact with parents concerning crying, shaking and abuse; (5) To reduce the incidence of physical abuse and shaken baby syndrome under one year; (6) To have the Period of PURPLE Crying program adopted as a nationwide early intervention project.

Eligibility

Ages Eligible for Study:  up to  4 Weeks,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • Subjects must be new parents or parents to be who are either: 1) attending participating prenatal classes; 2) delivering a baby at the participating hospital; or 3) visiting a PSPRN (Puget Sound Pediatric Research Network) pediatrician for infant care.
  • Only parents of infants born at > 34 weeks gestation are eligible.

Exclusion Criteria:

  • Parents of infants who have serious medical conditions.
  • Parents who don’t speak and read English.
  • Parents of infants born at < 34 weeks gestation.

Location and Contact Information


Washington
      Harborview Injruy Prevention and Research Center, Seattle,  Washington,  98104,  United States; Recruiting
Frederick P Rivara, MD  206-744-9449    fpr@u.washington.edu 
Frederick P Rivara, MD,  Principal Investigator
James taylor, MD,  Sub-Investigator
Liliana Lengua, PhD,  Sub-Investigator
Ron Barr, MD,  Sub-Investigator
Marilyn Sandberg, BA,  Sub-Investigator

More Information

http://www.hiprc.org

Study ID Numbers:  HIPRCSBS-01
Record last reviewed:  March 2005
Last Updated:  March 21, 2005
Record first received:  March 18, 2005
ClinicalTrials.gov Identifier:  NCT00105963
Health Authority: United States: Institutional Review Board (Awaiting confirmation)
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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Page Updated: September 6, 2005
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