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Clinical Trials/NCT05653414
NCT05653414
Not yet recruiting
Not Applicable

Interest of a Short Early Psychological Care in Women With Miscarriage: a Controlled Randomized Study

Université de Reims Champagne-Ardenne0 sites932 target enrollmentMay 30, 2023
ConditionsMiscarriage

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Miscarriage
Sponsor
Université de Reims Champagne-Ardenne
Enrollment
932
Primary Endpoint
anxiety
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

Miscarriage is a very common complication of pregnancy, accounting for 15.3% (95% CI 12.5-18.7%) of diagnosed pregnancies. Miscarriage would affect one in ten women during her lifetime. Worldwide, 23 million miscarriages occur annually.

Because of its frequency, miscarriage isoften considered as trivial event by caregivers. Still, miscarriage can be a traumatic event. Literature is consistent on the psychological morbidity associated with miscarriage. Anxiety, depression, post-traumatic stress have been studied in women after miscarriage. Cohort studies and clinical trials suggest that psychological and supportive interventions performed in women after miscarriage may improve women's psychological well-being and reduce miscarriage complications in subsequent pregnancies. However, to date, the literature is considered insufficient on the psychological care of women after a miscarriage.

Detailed Description

The aim of the study will be to evaluate the interest of a short early psychological care in women with miscarriage.

Registry
clinicaltrials.gov
Start Date
May 30, 2023
End Date
December 1, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Université de Reims Champagne-Ardenne
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • women with an early miscarriage (defined by a spontaneous termination of pregnancy before the 14th week of amenorrhea)
  • women aged more than 18
  • women agreeing to participate in the study (signing the informed consent form).

Exclusion Criteria

  • ectopic pregnancy
  • molar pregnancy
  • women with recurrent miscarriages
  • women less than 18

Outcomes

Primary Outcomes

anxiety

Time Frame: Month 3

Anxiety will be evaluated using the Scale Trait Anxiety Inventory version Y (STAI-Y-A). The STAI Form Y-A consists of a set of twenty item sonly focus on the psychological and not the somatic aspects of anxiety. The STAI Form Y-A is a self-reported questionnaire. Each item is scored from 1 to 4 and a sum score of all items is computed. Higher score indicates greater anxiety. Presence of anxiety will be defined by a score greater than or equal to 46.

Secondary Outcomes

  • depression(month 6)
  • anxiety(month 6)

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