Post-traumatic Stress Disorder in Spontaneous Abortion

Recruiting Observational Study
Spontaneous Abortion
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 45
Sex
Female
Study type
Observational
Participants needed
200 (estimated)
Sponsor
Jagiellonian University · Other
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About This Trial
The objective of this questionnaire-based study is to prospectively assess the prevalence of post-traumatic stress disorder (PTSD) symptoms in a population of women who have experienced a spontaneous miscarriage during the first trimester of pregnancy. The investigation into the prevalence of PTSD symptoms will assist in better identifying women who may benefit from early psychological interventio…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * spontaneous abortion * gestational age up to 14 weeks. Exclusion Criteria: * none
Contacts

Iwona Gawron, PhD, MD

+48 12424870

iwona.gawron@uj.edu.pl

CONTACT

Robert Jach, Prof., PhD

+48 12424871

jach@cm-uj.krakow.pl

CONTACT