Impact of Videoconference Updates in Neonatal Intensive Care Unit on Parental Stress of Preterm Infants (VISIO-NEONAT)

NCT ID: NCT03438071

Last Updated: 2020-06-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

28 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-02-21

Study Completion Date

2018-09-07

Brief Summary

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The aim of the study is to test the effect of daily videoconference updates between parents of preterm newborns and health care providers which also offer them the possibility of seeing their child on the parental stress in a neonatal intensive care unit (NICU).

Detailed Description

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Conditions

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Preterm Infants Parent-Child Relations Parental Stress Post Partum Depression Neonatal Intensive Care Units Videoconferencing

Study Design

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Observational Model Type

OTHER

Study Time Perspective

PROSPECTIVE

Study Groups

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Control group

No interventions assigned to this group

Videoconference group

Videoconferencing

Intervention Type OTHER

Daily videoconference updates using Skype between parents of preterm infants hospitalized in NICU and the nurse taking care of their child, lasting 5 to 10 minutes, to check with her for the daily news and then see their child through the camera.

Interventions

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Videoconferencing

Daily videoconference updates using Skype between parents of preterm infants hospitalized in NICU and the nurse taking care of their child, lasting 5 to 10 minutes, to check with her for the daily news and then see their child through the camera.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Parents with a preterm child born between 24 weeks and 34 weeks and 6 days of gestational age, hospitalized in our NICU during recrutment period
* Which agreed participating to the study after having complete information about it and sign a consent.

Exclusion Criteria

* Parents with a preterm child with another pathology than prematurity or with a lenght of stay in the NICU less than 7 days
* Parents refusing to participate to the study
* Parents not having videoconference equipment or internet access at home
* Parents not understanding or speaking good enough French.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Poitiers University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Denis Oriot

Role: PRINCIPAL_INVESTIGATOR

Poitiers University Hospital

Locations

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CHU DE Poitiers

Poitiers, , France

Site Status

Countries

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France

Other Identifiers

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VISIO-NEONAT

Identifier Type: -

Identifier Source: org_study_id

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