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Relationship Between Postpartum Mood Disorders and Delivery Experience

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University of Michigan

Status

Completed

Conditions

Stress Disorders, Post-Traumatic
Depression
Postpartum Period

Study type

Observational

Funder types

Other

Identifiers

NCT03004872
HUM00119428

Details and patient eligibility

About

The purpose of this study is to evaluate potential risk factors for developing postpartum depression or posttraumatic stress disorder during the first year postpartum in patients who have no preexisting history of PTSD or PPD.

Full description

It is theorized that poor pain control during labor and cesarean delivery, non-elective inductions, unplanned surgeries such as urgent/emergent cesarean delivery or operating room management of postpartum hemorrhage, and opioid abuse/addiction are risk factors for developing postpartum depression (PPD) or post-traumatic stress disorder (PTSD) after delivery. This study will, through questionnaires, interviews, and examination of the medical record, seek to identify whether and how strongly such correlations exist during the first year postpartum in patients who have no preexisting history of these conditions.

Enrollment

600 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Woman planning on giving birth at the University of Michigan
  • Speaks English without translator
  • Live pregnancy not desiring termination
  • Smartphone owner
  • Woman whose delivery date is >28 weeks gestational age

Exclusion criteria

  • History of previous postpartum depression (PPD) or posttraumatic stress disorder (PTSD) from a birth experience
  • Non-English speaker requiring a translator
  • Patients who have a fetus with major fetal anomalies
  • Positive screening at 28 weeks antepartum for Edinburgh Postnatal Depression Scale (EPDS) or Primary Care PTSD (PC-PTSD) screen

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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