CClinicalTrials.gg
CompletedNCT06771661Updated Aug 31, 2026

Parents' Experience of Child Loss During Pregnancy or Birth

An observational study in Stillbirth and Fetal Death, Miscarriages and Experience, sponsored by Fritz Sterr. Completed at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-31.

Sponsored by Fritz Sterr · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
46
Ages
18 Years and older
Sex
All
01

Study summary

The investigators are conducting a participatory study with and for parents after child loss during pregnancy or birth. Their aim is to develop treatment recommendations for healthcare professional. These focus on question, how to deal with parents when experiencing child loss.

Read the detailed description

The entire study is following a participatory approach and including parents after stillbirth in the research team. Along a co-creative design, the investigators planned a multistep-explorative mixed-methods study.

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.

02

Conditions studied

  • Stillbirth and Fetal Death
  • Miscarriages
  • Experience

Keywords

  • Pregnancy loss
  • Child loss
  • Qualitative research
  • Mixed-methods
  • Experience
  • Need
  • Parents
  • Perinatal loss
  • Fetal death
  • Miscarriage
  • Stillbirth
03

In context

Stillbirth

117 studies on the registry are indexed under Stillbirth; 33 are open to participants now.

This study's enrollment of 46 is below the median of 794 across 50 observational studies indexed under Stillbirth.

Browse Stillbirth studies →

Lead sponsor

This is the only study on the registry with Fritz Sterr as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Parents (mothers, fathers) will be recruited that lost their child during pregnancy or birth in hospitals, at home or birth houses.

Inclusion criteria

  • German speaking
  • Living in Austria, Germany or Switzerland
  • Child loss during pregnancy or birth
  • Child loss within last 12 months
  • Legal capacity
  • Voluntary participation

Exclusion criteria

Exclusion Criteria:

  • Loss of child after birth
  • Not speaking and understanding German
  • Not in a good mental condition to participate
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
46 participants (actual)
Patient registry
No

Groups and cohorts

  • Parents after intrauterine or perinatal child loss

    Other: Workshops · Other: Focus group interviews · Other: Narrative interviews · Other: Delphi approach

Interventions

  • OtherWorkshops

    The investigators will conduct workshops with parents to get closer to the main topic.

  • OtherFocus group interviews

    The investigators will conduct focus group interviews with parents on their needs before and during child loss.

  • OtherNarrative 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.

  • OtherDelphi 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.

06

What researchers measure

Primary outcomes

  1. Parent's experience

    The investigators are interested in parents' in-depth and lived experience before and during their intrauterine or perinatal child loss.

    Time frame: During pregnancy and up to 7 days after birth

Secondary outcomes

  1. Parents' subjective needs

    In qualitative interviews, the subjective needs that parents developed before and during their intrauterine or perinatal child loss will be investigated.

    Time frame: During pregnancy and up to 7 days after birth

07

Study locations

1 site
  • Deggendorf Institute of Technology, Faculty of Applied Healthcare Sciences
    Deggendorf, Bavaria 94469, Germany
08

References and documents

Publications

  • Sterr F, Siepmann J, Nuber-Fischer D, Rester C, Gensheimer K, Bauernfeind L. Parents' experience of child loss during pregnancy or birth: protocol for an explorative, sequential and participative mixed-methods study. Res Involv Engagem. 2025 Dec 5;11(1):139. doi: 10.1186/s40900-025-00819-8. PubMed 41350907 ↗
  • Siepmann J, Bauernfeind L, Nuber-Fischer D, Rester C, Gensheimer K, Sterr F. Needs of parents during their intrauterine or perinatal child loss - a qualitative multi-method study. BMC Public Health. 2026 May 12;26(1):1526. doi: 10.1186/s12889-026-27687-5. PubMed 42121131 ↗

Individual participant data

Plan to share: No — The data to be collected is particularly sensitive and is stored securely and deleted after the study. Individual pseudonymised excerpts are made public in the publications.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06771661
Lead sponsor
Fritz Sterr
Responsible party
Fritz Sterr (Research associate, Deggendorf Institute of Technology, Faculty of Applied Healthcare Sciences) — Sponsor-investigator
First posted
Jan 13, 2025
Start date
Dec 2, 2024
Primary completion
Jul 17, 2025
Completion
Aug 1, 2026
Last update
Aug 31, 2026

Study contacts

Christian Rester, Prof. Dr.
study chair · Deggendorf Institute of Technology

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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