Screening for Depression and Anxiety in Pregnant and Postpartum Women: Evaluating Prevalence, Risk Factors, and the Stepped Screening Protocol in a Care Pathway

NCT06664593 | Completed

• 1 other identifier: 198215
• Study Type: observational
• Target: 378
• Locations: 1 country
• Sites: 1

Brief Summary

Having a baby is a major life event, and for some women, it can increase the risk of developing mental health issues. A recent survey in the UK found that one in five women experience mental health problems during pregnancy or after giving birth. Unfortunately, many of these problems go unnoticed without regular check-ups, and only one in ten women receive the support they need. Regular mental health screenings can help detect these problems early, ensuring women receive the right care and support. The study at UZ Gent aims to improve how depression and anxiety are detected in pregnant and postpartum women by using a perinatal screening protocol. This protocol involves screening women for psychosocial risks around the 16th week of pregnancy, which is done by a midwife. Further screenings take place during the second trimester (around 20 weeks) and again six weeks after birth, using questionnaires to assess for depression and anxiety (Whooley, EPDS, GAD-2, GAD-7). If the assessment of risk factors or the screening for depression and anxiety is positive, further assessment and treatment are offered at the women\'s clinic. A positive screening may lead to a recommendation for a diagnostic interview, such as a semi-structured interview (M.I.N.I.), with a psychiatrist, general practitioner, or psychologist to assess for possible depression or anxiety disorders. If needed, appropriate treatment will be provided. The study will explore how common depression and anxiety are during and after pregnancy, what factors increase the risk, and whether the screening process improves early detection and treatment. The ultimate goal is to help more women get the mental health support they need during this critical time.

Conditions

Depression, Postpartum; Puerperal Disorders; Depression During Pregnancy; Anxiety; Anxiety Disorder/Anxiety State; Stress, Psychological; Risk Factors

Outcome Measures

Primary Outcomes (2)

• association of psychosocial and obstetric risk factors with perinatal anxiety and depression

  Using a semi-structured interview, the midwife assesses psychosocial risk factors identified from a literature review. Key factors include financial and housing problems, unplanned or unwanted pregnancy, lack of social support, experiences of violence (physical, sexual, or emotional), personal and family psychiatric history, and substance use. Screening for depressive and anxiety symptoms followed a stepped protocol. All participants answered Yes/No to the Whooley questions (depression) and GAD-2 (anxiety). If a participant answered positively to at least one Whooley question or both GAD-2 questions, the Edinburgh Depression Scale (EDS) was administered. A score of 13 or higher on the EDS indicated a positive depression screen. If participants scored 5 or higher on the EDS-3A (anxiety subscale), the GAD-7 was administered, with a score of 15 or higher indicating a positive anxiety screen. Obstetric information was collected from the electronic patient medical records.

  from enrollment at 16 weeks of pregnancy to follow-up consult at 6-8 weeks postpartum

• association between the number of (significant) risk factors and depressive and anxiety symptoms using a cumulative risk index

  from enrollment at 16 weeks of pregnancy to follow-up consult at 6-8 weeks postpartum

Secondary Outcomes (1)

• prevalence of depressive and anxiety symptoms

  from enrollment at 16 weeks of pregnancy to follow-up consult at 6-8 weeks postpartum

Study Arms (1)

women in the perinatal period, from pregnancy until 6-8 weeks postpartum

women from pregnancy until 6-8 weeks postpartum with and without mental health problems

Other: integrated perinatal mental health pathway

Interventions

integrated perinatal mental health pathway OTHER

This observational study examines whether assessing psychosocial risk factors and screening for depression and anxiety at different time points during the perinatal period, using a stepped protocol, helps to more quickly detect women with depressive and anxiety symptoms.

women in the perinatal period, from pregnancy until 6-8 weeks postpartum

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

The study population consists of women receiving regular care during pregnancy and postpartum follow-up at the women\'s clinic of University Hospital Ghent

You may qualify if:

• Pregnant women aged ≥ 18 years, receiving regular care follow-up in a university hospital

You may not qualify if:

• Non-Dutch speakers were excluded. Additionally, no data were collected from women in the vulnerable care pathway, which provides psychosocial support to those facing barriers in employment, income, housing, education, and healthcare. This group includes teenage mothers (under 18), women with intellectual disabilities, new immigrants, refugees, homeless women, and those with severe psychiatric or addiction issues referred by their psychiatrist or GP.

Sponsors & Collaborators

• University Hospital, Ghent: lead

Study Sites (1)

University Hospital Ghent

Ghent, Belgium

Location

Related Publications (1)

• Van Damme R, Van Parys AS, Vogels C, Roelens K, Lemmens GMD. A mental health care protocol for the screening, detection and treatment of perinatal anxiety and depressive disorders in Flanders. J Psychosom Res. 2020 Jan;128:109865. doi: 10.1016/j.jpsychores.2019.109865. Epub 2019 Nov 1. No abstract available.

  PMID: 31838308 BACKGROUND

MeSH Terms

Conditions

Depression, Postpartum; Puerperal Disorders; Anxiety Disorders; Stress, Psychological

Condition Hierarchy (Ancestors)

Pregnancy Complications; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Depressive Disorder; Mood Disorders; Mental Disorders; Behavioral Symptoms; Behavior

Study Officials

• Gilbert Lemmens, PhD

  University Hospital Ghent/University Ghent

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 34 Weeks
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 28, 2024
• First Posted: October 29, 2024
• Study Start: November 20, 2018
• Primary Completion: February 18, 2020
• Study Completion: July 30, 2020
• Last Updated: October 29, 2024

Record last verified: 2024-10

Data Sharing

• IPD Sharing: Will not share

Locations

BE (1)