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Motives, Awareness and Memories of participation in Pediatric Anesthesia Research

Motives, Awareness and Memories of participation in Pediatric Anesthesia Research - MAMA`s & PAPA`s

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033384
Enrollment
600
Registered
2024-01-09
Start date
2024-03-27
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

Legal guardians and their children who have been recruited by our study group for a clinical trial in paediatric anaesthesia in the past

Interventions

Group 1: Digital questionaire survey of legal guardians and their children who have been recruited by our study group for a clinical trial in paediatric anaesthesia in the past

Sponsors

Universitätsmedizin Göttingen, Klinik für Anästhesiologie
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All legal guardians whose children have taken part in a clinical study conducted by the Paediatric Anaesthesiology working group at the Department of Anaesthesiology at the University Medical Centre Göttingen in the last five years will be contacted by post. The patients were under the age of 18 at the time. Only completely finalised questionnaires are included in the analysis of this study project.

Exclusion criteria

Exclusion criteria: As the participation in the questionnaire study requires the guardians to become active (by opening a web link to the questionnaire), there are no exclusion criteria.

Design outcomes

Secondary

MeasureTime frame
1. correlation of the degree of concern about anaesthesia/sedation or intervention/examination (measured on a scale of 1 to 5) with satisfaction with the previous study participation 2. level of knowledge of the guardians about the results of the previous study participation 3. level of knowledge of the custodians about the possibility of cancellation and voluntariness of the previous study participation 4. quality assurance aspects of the informed consent process for the previous study participation 5. comparison of the respective parameters with regard to the different study types, localisations and times

Primary

MeasureTime frame
Overall satisfaction with the experience from the previous study participation (measured on a scale from 1 = very dissatisfied to 10 = very satisfied.

Countries

Germany

Contacts

Public ContactMarcus Nemeth

Universitätsmedizin Göttingen, Klinik für Anästhesiologie

marcus.nemeth@med.uni-goettingen.de+49 551 3967701

Outcome results

None listed

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