Impact of Information Campaign's Alongside Maternity Staff About Bedding Infant

Sponsor
CHU de Reims (Other)
Overall Status
Completed
CT.gov ID
NCT03934242
Collaborator
(none)
300
1
3
99.3

Study Details

Study Description

Brief Summary

It is now well established that infants should be placed on the back only in a SleepSack without coverage or plush or pillow on a firm mattress in a bedroom. Despite these old recommendations of good practice, deviations are observed and some infants are most always lying according to the recommended position. The goal is to assess the impact of an information campaign of staffs maternity of the CHU of Reims on the practices of the sleeping of infants to motherhood, and then at the home of the parents.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaire on new born's bedding

Detailed Description

Proposal for participation to the holders of parental authority of newborns eligible within 72 hours after the birth of the child. If acceptance of participation, the newborn will be included in the study. Participation in the study will not affect the medical care of the child. Participation in the study will consist of: a collection of data including the child sleeping mode, complete a questionnaire covering the child sleeping habits to motherhood and home during the 1st month of life. Information on the habits of sleeping in the home of the child will be collected via a phone call by an investigator. Inclusions will be held over 2 periods: one before and one after the completion of training of health care personnel regarding the sleeping of infants nursing staff training will consist of oral information by the investigative team and written information...

Study Design

Study Type:
Observational
Actual Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Impact of Information Campaign's Alongside Maternity Staff About Bedding Infant
Actual Study Start Date :
Mar 5, 2019
Actual Primary Completion Date :
May 5, 2019
Actual Study Completion Date :
Jun 5, 2019

Arms and Interventions

Arm Intervention/Treatment
New born group 1

New born who was born at the maternity of the CHU of Reims during a period of inclusion of one month, before nurses formation on the newborn's bedding

Other: Questionnaire on new born's bedding
Questionnaire on new born's bedding (Child's position in the bed : dorsal, ventral or lateral, presence of pillow or stuffed in bed, presence of coverage and presence of the bed sharing) at two times (during hospitalisation and one month later)

New born group 2

New born who was born at the maternity of the CHU of Reims during a period of inclusion of one month, after nurses formation on the newborn's bedding

Other: Questionnaire on new born's bedding
Questionnaire on new born's bedding (Child's position in the bed : dorsal, ventral or lateral, presence of pillow or stuffed in bed, presence of coverage and presence of the bed sharing) at two times (during hospitalisation and one month later)

Outcome Measures

Primary Outcome Measures

  1. correct new born's bedding [Day 0]

    Newborn's bedding will be considered correct if the newborn is lying alone (no bed sharing), in exclusive dorsal position (no ventral or lateral position), in a bed without pillow, without blanket and without soft toy.

  2. correct new born's bedding [month 1]

    Newborn's bedding will be considered correct if the newborn is lying alone (no bed sharing), in exclusive dorsal position (no ventral or lateral position), in a bed without pillow, without blanket and without soft toy.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 1 Month
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • born in reims CHU

  • parents are 18 years old or more

  • parents accept their participation in the study

Exclusion criteria :
  • hospitalization in URIP / kangourou / neonatalogy

  • needed baby warmer

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chu Reims Reims France 51092

Sponsors and Collaborators

  • CHU de Reims

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
CHU de Reims
ClinicalTrials.gov Identifier:
NCT03934242
Other Study ID Numbers:
  • PO19012
First Posted:
May 1, 2019
Last Update Posted:
Jul 24, 2019
Last Verified:
Apr 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 24, 2019