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Maternal preferences in decision making for infants born near the limit of viability

Maternal preferences in decision making for infants born near the limit of viability - PREFAB

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00013034
Enrollment
64
Registered
2017-11-09
Start date
2017-12-06
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infants born near the limit of viability

Interventions

Group 1: A written case scenario of an imminent preterm birth at the limit of viability will be presented. The difficulties of the decision-making making process as well as short- and long-term outcom

Sponsors

Universitätsmedizin Mainz
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Pregnant women between 28 + 0 and 36 + 6 weeks of gestation; inpatient treatment due to imminent premature birth; interdisciplinary (obstetrics and paediatrics) antenatal counselling done

Exclusion criteria

Exclusion criteria: missing consent; severe fetal malformation; possible postnatal palliative therapy; insufficient knowledge of German language; mental illness, lack of ability to consent

Design outcomes

Primary

MeasureTime frame
Proportion of subjects with a preference for life-sustaining intensive care after birth

Secondary

MeasureTime frame
Proportion of subjects who do not formulate a preference; Degree of desired participation in decisions at the limit of viability; Preference of the subjects to involve other persons in the decision making process; Assessment of risks and benefits of life-sustaining intensive care treatments; Association of age, educational level, religion, marital status, etc. with the preference for life-sustaining intensive care Treatments; The given endpoints are recorded by means of a questionnaire which has to be answered once and within 24 hours after the presentation of the case. The questionnaire is identical in both study arms and consists of selection questions and gradual questions (collected with a 5-point Likert scale). The participants have the opportunity to freely formulate important thoughts at the end of the questionnaire.

Countries

Germany

Contacts

Public ContactAndré Kidszun

Universitätsmedizin MainzZentrum für Kinder- und Jugendmedizin

andre.kidszun@unimedizin-mainz.de06131 17 5892

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026