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EEG Alterations of Uterine Contractions in the First Stage of Labor Predicting Postpartum Depression

Z

Zhujiang Hospital

Status

Enrolling

Conditions

Postpartum Depression

Treatments

Other: frontal alpha asymmetry in EEG

Study type

Observational

Funder types

Other

Identifiers

NCT05217251
Maternal EEG monitoring

Details and patient eligibility

About

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.

Full 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.

Enrollment

330 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

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.

Trial design

330 participants in 2 patient groups

exposed group
Description:
Parturient women will be identified with frontal alpha asymmetry based on EEG monitoring of uterine contractions in the first stage of labor and will then be allocated to vaginal delivery with alpha asymmetry group in hospital.
Treatment:
Other: frontal alpha asymmetry in EEG
control group
Description:
Parturient women will be identified without frontal alpha asymmetry based on EEG monitoring of uterine contractions in the first stage of labor and will then be allocated to vaginal delivery without alpha asymmetry group in hospital.
Treatment:
Other: frontal alpha asymmetry in EEG

Trial contacts and locations

1

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Central trial contact

HongFei Zhang, MD PhD; FengXian Li, MD PhD

Data sourced from clinicaltrials.gov

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