Childbirth Related Fear and Worry During Pregnancy

Anxiety Clinical Trial

Official title: Childbirth Related Fear and Worry During Pregnancy

Status Active, not recruiting

Clinical Trial Summary

This is a study of childbirth related anxiety, fear or worry, in which we follow women from mid pregnancy until about 8 months postpartum. Our overall aim is to enhance our understanding of psychological factors contributing to childbirth related fear or worry. Specifically, we wish to investigate

• associations between psychological factors (pain catastrophizing, intolerance of uncertainty, worry beliefs, cognitive avoidance, insomnia, life satisfaction, anxiety- and depressive symptoms, worry parameters, and behavioral avoidance) and childbirth related fear or anxiety during pregnancy

• the impact of childbirth related fear or anxiety and other psychological factors during pregnancy on epidural use during delivery and obstetric outcome variables

• childbirth related fear or anxiety during pregnancy, psychological factors, epidural use, and obstetric outcome variables as predictors of self-reported birth experiences 6-10 months postpartum.

• childbirth related fear or anxiety during pregnancy, psychological factors, epidural use, obstetric outcome variables, and self-reported birth experiences as predictors of childbirth related fear or anxiety 6-10 months postpartum

Women in mid-pregnancy will be recruited at routine check-ups with midwifes working in antenatal health care units in two Swedish regions. After consenting to participate, they will be answering a questionnaire with sociodemographic and obstetric background data, measures of childbirth related fear and anxiety, and measures of psychological variables with a potential relation to childbirth related anxiety. 6-10 months after giving birth they will be contacted again with a postpartum follow-up questionnaire asking questions about the experience of giving birth, postpartum levels of childbirth related fear or anxiety, and thoughts about possible future childbirths. They will also be asked if willing to let the research team include information from their obstetric medical chart (e.g. birth mode and birth interventions, use of analgesia, and complications for the mother and baby) in statistical analyses.

Clinical Trial Description

Aim and main research questions:

The overall aim with this study investigate psychological factors contributing to childbirth related fear or worry. Specifically, we wish to investigate

• associations between psychological factors (pain catastrophizing, intolerance of uncertainty, worry beliefs, cognitive avoidance, insomnia, life satisfaction, anxiety- and depressive symptoms, worry parameters, and behavioral avoidance) and childbirth related fear or anxiety during pregnancy

• the impact of childbirth related fear or anxiety and other psychological factors during pregnancy on epidural use during delivery and obstetric outcome variables

• childbirth related fear or anxiety during pregnancy, psychological factors, epidural use, and obstetric outcome variables as predictors of self-reported birth experiences 6-10 months postpartum.

• childbirth related fear or anxiety during pregnancy, psychological factors, epidural use, obstetric outcome variables, and self-reported birth experiences as predictors of childbirth related fear or anxiety 6-10 months postpartum

Procedure:

Pregnant women will be recruited by midwives working in antenatal health care units in two Swedish regions; Jämtland/Härjedalen and Örebro County. Recruitment is planned to take place during the first visit following the routine ultrasound examination (normally provided in gestational week 16-20). Women found not eligible will be counted by each antenatal midwife and reported to the project group without any personal identification. Before invited to participate, eligible women will be given oral and written information about the study. Any questions might be asked the midwife directly or via telephone or e-mail to the members of the research group. If accepting participation, each woman will give her written consent. The woman will then receive the first questionnaire. The questionnaire is coded with a unique code for each participant, and does not include any personal identification. It is returned to the research group in a pre-paid envelope. The consent form, also including the unique code of each participant, contact information and personal identification number, is collected by the midwife and later sent to the research group.

In phase two of the study, data will be gathered from two different sources - (a) from the medical birth records of the particular birth, and (b) via a postpartum follow-up questionnaire. These data will be gathered 6-10 months after the planned date of the birth. All women who have returned the first questionnaire and whose address can be confirmed will be contacted by mail and invited to participate in phase two. Letters will be sent, including information about phase two of the project, a postpartum follow-up questionnaire, and a consent form in which the woman can give her written consent for the research team to extract data from the medical birth record. The women are thus free to choose their participation in the two parts of phase 2 separately. The follow-up questionnaire and consent form will returned to the research group by mail, in a pre-paid envelope.

Extraction of medical data: Once consent has been received, obstetric data will be extracted from the medical chart, with help from a midwife at each hospital. The data will be anonymized before leaving the hospital, erasing all personal data such as name and personal identification number, coding the obstetric set of data with the unique participant code number of each woman.

Data and measurements:

The first questionnaire, in mid-pregnancy includes the following sections and scales:

• Sociodemographic background (age, civil status, educational level, occupational status, country of birth)

• Obstetric history/background (pregnancy week, number of fetuses, current pregnancy complications, previous births including birth mode and year)

• Negative experiences in health care

• Preferred mode of birth

• the Fear of Birth Scale, FOBS

• the Wijma Delivery Expectancy/Experience Questionnaire, W-DEQ A

• the Hospital Anxiety and Depression Scale, HADS

• the Pain Catastrophizing Scale, PCS

• the Intolerance of Uncertainty Inventory, part B

• Why Worry II

• the Cognitive Avoidance Questionnaire

• the Insomnia Severity Index, ISI

• the Satisfaction With Life Scale, SWLS

• the Situational Fear of Childbirth, SFC

• items regarding worry frequency, controllability and excess from the GAD-7

• items regarding childbirth specific behavioral avoidance

The postpartum follow-up questionnaire includes:

• Birth information (birth date, birth mode including indication, usage of epidural analgesia)

• the Wijma Delivery Expectancy/Experience Questionnaire, W-DEQ A

• the Fear of Birth Scale, FOBS

• The Childbirth Experience Questionnaire

• Two visual analogue scales regarding the experience of giving birth (vaginally or with Caesarean section) using the anchors "not at all positive" to "very positive" and "not at all negative" to "very negative".

• One visual analogue scale regarding the worst experience of pain during birth, using the anchors "not painful at all" and "worst pain possible".

• One visual analogue scale regarding overall experience of pain during birth, again using the anchors "not painful at all" and "worst pain possible".

• Preferred mode of birth in a future birth

Medical birth data that will be extracted:

• Age of the mother, parity, and gestational week

• Comorbidity

• Obstetric and neonatal outcome variables (see outcome measures) ;

Related Conditions & MeSH terms

• Anxiety
• Fear of Childbirth

• NCT number: NCT03353168
• Study type: Observational
• Source: Mid Sweden University
• Status: Active, not recruiting
• Phase: N/A
• Start date: September 1, 2015
• Completion date: January 30, 2018