Attachment Bonding and Neonatal Hospitalization: the Impact of Hospitalization in a Kangaroo Unit
NCT ID: NCT06243861
Last Updated: 2024-05-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
96 participants
OBSERVATIONAL
2024-04-10
2025-04-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Assessment of Autonomic Co-regulation Between Newborn and Parent During Kangaroo Care Sessions in Neonatal Intensive Care Units
NCT03690804
Impact of Providing Nursing Support on Parental Stress Related to Preoperative Care of a Newborn with Hirschsprung's Disease
NCT06650683
Promoting Kangaroo Care for Preterm or Low Birthweight Infants in Rural India
NCT07231432
Kangaroo Position in Preterm Newborn Infants Under Oxygen Therapy
NCT06170892
Effect of Kangaroo Mother Care Versus Hammock Positioning
NCT05165004
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
kangaroo unit
Mother-child bond
assessing whether the mother-child bond is degraded in the UK, in comparison with that of mothers in post-natal care
postnatal care
Mother-child bond
assessing whether the mother-child bond is degraded in the UK, in comparison with that of mothers in post-natal care
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Mother-child bond
assessing whether the mother-child bond is degraded in the UK, in comparison with that of mothers in post-natal care
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Affiliated to a social security scheme,
* fluent in French
* no objection of participation
Exclusion Criteria
* given birth to a child who was stillborn or died at birth
* difficulty understanding written French
* psychological incapacity (psychiatric disorder, too great a vulnerability) or physical incapacity (physical/motor disability) to answer questionnaires,
* Patient under court protection, guardianship or curatorship.
18 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centre Hospitalier Régional Metz-Thionville
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Marie-Laure BOYE
Role: PRINCIPAL_INVESTIGATOR
CHR Metz Thionville
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHR Metz-Thionville/Hopital Mercy
Metz, , France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2023-08Obs-CHRMT
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.