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Clinical Trials/NCT05217251
NCT05217251RecruitingNot Applicable

The Values of Electroencephalography (EEG) Alterations of Uterine Contractions in the First Stage of Labor Predicting Postpartum Depression: a Prospective Cohort Study

Zhujiang Hospital1 site in 1 country330 target enrollmentStarted: March 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
330
Locations
1
Primary Endpoint
The incidence of depression in 12 months after childbirth.

Study Overview

Brief Summary

Severe uterine contractions in labor can trigger emotional disorders including postpartum depression in women during the puerperium. Numerous studies have shown that resting frontal electroencephalogram (EEG) asymmetry is closely related to depression. Therefore, the investigators hypothesize that the frontal alpha asymmetry in EEG during uterine contractions in the first stage of labor be associated with the risk level of postpartum depression. The objective of this research is to investigate, in a 1-year period, the incidence of postpartum depression in natural birth mothers in relation to frontal alpha asymmetry in EEG during uterine contractions and resting state.

Detailed Description

Severe uterine contractions in labor can trigger emotional disorders including postpartum depression in women during the puerperium. It is characterized by lack of motivation and behavioral changes, potentially producing serious negative consequences for offspring.

In addition, EEG alpha asymmetry is one of the commonly studied biomarkers for depression. There are multiple previous studies regarding the symmetry of EEG in left and right brain hemispheres, especially at frontal electrodes. Besides, there are many other EEG indicators that predict depression which are also likely to be strong contributors to postpartum depression.

The objective of study is to investigate if there is any association between EEG alterations of uterine contractions in the first stage of labor and factors that are associated with postpartum depression.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • parturient women with a singleton pregnancy;
  • capable of understanding the research requirements and willing to cooperate with the study instructions;
  • aged 18-45;
  • American Society of Anesthesiologists(ASA) physical status I or II;
  • right handed;
  • not taking any drug known to influence the EEG;
  • EPDS scale (Edinburgh Postnatal Depression Scale, EPDS) is used in the last prenatal examination in outpatient clinics , with scores < 10;
  • informed consent is gained from all individual subjects taking part in the study.

Exclusion Criteria

  • history of neurological or psychiatric disease;
  • personality disorder;
  • cerebral disease;
  • epidural anesthesia contraindication;
  • multiparous pregnancy.

Outcomes

Primary Outcomes

The incidence of depression in 12 months after childbirth.

Time Frame: up to 12 months after childbirth.

Postpartum depression in 12 months is diagnosed by using Edinburgh Postpartum Depression Scale (EPDS) by a research assistant. the threshold of postpartum depression is defined as a score of ≥10.The EPDS is a 10-item self-report scale to screen for Postnatal Depression. The EPDS is found to have satisfactory sensitivity and specificity, and is also sensitive to change in the severity of depression over time. Each question is on a scale of 0 to 3. The EPDS has a score range between 0 to 30, with a higher score reflecting higher symptom severity in depression.

Secondary Outcomes

  • The score of pain in 12 months after childbirth(up to 12 months after childbirth.)

Investigators

Sponsor
Zhujiang Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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