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COMPLETEDNANCT02736136

An Early Intervention to Increase Maternal Self-efficacy After Preterm Birth

This study aims to investigate the effects of an early intervention (joint observation and video feedback) on maternal parenting self-efficacy following a premature birth. Mothers who have given birth...

Lead sponsor: Centre Hospitalier Universitaire Vaudois•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Centre Hospitalier Universitaire Vaudois

Age

18 - 65 years

Sex

FEMALE

Healthy Volunteers

Yes

Inclusion Criteria

•Mothers of very preterm infants born between 28 and 32 weeks of gestation
•Infant aged up to 8 weeks

Exclusion Criteria

•Do not speak French sufficiently well to participate in assessments
•Have established intellectual disability or psychotic illness
•Infant too instable regarding hemodynamic or respiratory functioning (severe brady apnea, more than 30% oxygen)

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: March 25, 2022Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment71

Start dateAug 2016

Last updatedMar 25, 2022

Condition

Posttraumatic Stress Disorder Stress Anxiety Depression

Locations shown

Neonatology Service, University Hospital Lausanne

Lausanne, Canton of Vaud

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 25, 2022Data synced to Clareo: June 27, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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