Parents' Experience of Child Loss During Pregnancy or Birth
NCT ID: NCT06771661
Last Updated: 2025-01-13
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
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RECRUITING
50 participants
OBSERVATIONAL
2024-12-02
2026-12-31
Brief Summary
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Detailed Description
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In detail, three key steps will be conducted. First, workshops and focus groups will be carried out to identify central needs of affected parents. Afterwards, one investigator will interview the parents narratively to gain an in-depth understanding of their experiencs. Finally, these findings will be summarized and translated into treatment recommendations for healthcare professionals.
Conditions
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Study Design
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OTHER
OTHER
Study Groups
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Parents after intrauterine or perinatal child loss
Workshops
The investigators will conduct workshops with parents to get closer to the main topic.
Focus group interviews
The investigators will conduct focus group interviews with parents on their needs before and during child loss.
Narrative interviews
The investigators will conduct narrative interviews with parents to gain an in-depth understanding of their lived experience before and during the intrauterine or perinatal child loss.
Delphi approach
The investigators will carry out a Delphi approach with parents to translate and confirm or revise the findings into treatment recommendations for healthcare professionals.
Interventions
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Workshops
The investigators will conduct workshops with parents to get closer to the main topic.
Focus group interviews
The investigators will conduct focus group interviews with parents on their needs before and during child loss.
Narrative interviews
The investigators will conduct narrative interviews with parents to gain an in-depth understanding of their lived experience before and during the intrauterine or perinatal child loss.
Delphi approach
The investigators will carry out a Delphi approach with parents to translate and confirm or revise the findings into treatment recommendations for healthcare professionals.
Eligibility Criteria
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Inclusion Criteria
* Living in Austria, Germany or Switzerland
* Child loss during pregnancy or birth
* Child loss within last 12 months
* Legal capacity
* Voluntary participation
Exclusion Criteria
* Not speaking and understanding German
* Not in a good mental condition to participate
18 Years
ALL
No
Sponsors
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Fritz Sterr
OTHER
Responsible Party
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Fritz Sterr
Research associate
Principal Investigators
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Christian Rester, Prof. Dr.
Role: STUDY_CHAIR
Deggendorf Institute of Technology
Locations
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Deggendorf Institute of Technology, Faculty of Applied Healthcare Sciences
Deggendorf, Bavaria, Germany
Countries
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Central Contacts
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Facility Contacts
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Fritz Sterr, M.Sc.
Role: backup
Julian Siepmann, M.Sc.
Role: backup
Lydia Bauernfeind, Ph.D.
Role: backup
Related Links
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Landing Page of the Study
Other Identifiers
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GEHBa-202409-V-237-R2
Identifier Type: -
Identifier Source: org_study_id
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