Maternal Mental Health

Sponsor
Michelle Lopez (Other)
Overall Status
Completed
CT.gov ID
NCT03777046
Collaborator
(none)
545
2
3
15.9
272.5
17.1

Study Details

Study Description

Brief Summary

Perinatal (around the time of birth) mental health disorders are common difficulties of pregnancy. Perinatal depression is made up of major and minor depressive events during pregnancy and the first 12 months after delivery. It is estimated that 11%-19% of mothers suffer from perinatal depression. However, rates may be significantly higher among some subpopulations.

Left untreated, post partum depression (PPD) is linked with several significant negative health impacts on the mother, her infant, and their families. PPD is linked with lower quality maternal-child relationship, and this change in emotional attachment can lead to physiologic changes and poorer cognitive outcomes in the infant.

The purpose of this study is to determine the maternal mental health effect of postpartum depression screening and intervention during infants' short term hospitalizations. The study is also aiming to define effects of PPD short term hospitalization interventions on maternal PPD follow up and child health based on well child care (WCC), emergency department (ED) visits, hospital readmissions, and parent's feelings on child's health.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Standard of Care (SOC)
  • Behavioral: SOC with Psychology Therapy (CBT)
N/A

Detailed Description

Study participants will complete a survey about their general needs and access to resources and a survey to screen for postpartum depression to determine if the participant will be enrolled. Based on the answers provided, the study team may recommend that the participant seek additional medical care, and may notify the participant's doctor, the child's doctor, and hospital officials if the study team believes that the participant needs further medical care for depression.

Half of the study participants will receive a social work consult and treatment with psychology therapy in the hospital. The psychology therapy will be 2-3 fifty-minute therapy sessions while the child is in the hospital. An outpatient psychiatry/psychology follow up appointment will be offered if needed as per routine care.

Discharge Follow Up:

A discharge follow up questionnaire and survey will be completed on an electronic tablet around the time of the baby's discharge home from the hospital or within 1 week of being at home. The survey can be completed over the phone or it can be sent via email or text to complete the survey online.

One Month Follow Up:

A one-time follow up questionnaire and survey will be completed 1 month after discharge from the hospital. The survey can be completed in approximately 5 - 10 minutes over the phone or it can be sent via email or text to complete the survey online.

The other half of the study participants will receive social work consult with information about follow up options for PPD per current standard of care for mothers identified as having postpartum depression in the hospital setting.

As part of this study a review of the child's medical record, including data collection, will be performed.

Study Design

Study Type:
Interventional
Actual Enrollment :
545 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Addressing Maternal Mental Health Needs During Pediatric Acute Care Hospitalizations
Actual Study Start Date :
Jan 24, 2019
Actual Primary Completion Date :
Mar 13, 2020
Actual Study Completion Date :
May 22, 2020

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Screen fail subjects

Mothers and their babies that meet inclusion criteria for the study, but score less than 10 on the Edinburgh Postpartum Depression Scale (EPDS)

Active Comparator: PPD Control subjects

Mothers and their babies that meet inclusion criteria for the study, that score 10 or more on the Edinburgh Postpartum Depression Scale (EPDS) that will receive Standard of care treatment. SOC treatment includes social work consult with information about follow up options for PPD.

Behavioral: Standard of Care (SOC)
Mothers that meet inclusion criteria for the study, that score 10 or more on the Edinburgh Postpartum Depression Scale (EPDS) that will receive Standard of care treatment. SOC treatment includes social work consult with information about follow up options for PPD.

Experimental: PPD Intervention subjects

Mothers and their babies that meet inclusion criteria for the study, that score 10 or more on the Edinburgh Postpartum Depression Scale (EPDS) that will receive the experimental intervention. Intervention includes SOC treatment as well as psychology therapy (CBT) in the hospital.

Behavioral: SOC with Psychology Therapy (CBT)
Mothers that meet inclusion criteria for the study, that score 10 or more on the Edinburgh Postpartum Depression Scale (EPDS) that will receive the experimental intervention. Intervention includes SOC treatment as well as psychology therapy (CBT) in the hospital.

Outcome Measures

Primary Outcome Measures

  1. Difference in PPD score [at Month 1]

    PPD score will be measured using the Edinburgh Postnatal Depression Scale (EPDS). A score less than 8 suggests depression is not likely. A score of 9-11 suggests depression is possible. A score of 12-13 indicates fairly high possibility of depression. A score of 14 and higher suggest probable depression. Positive score of 1, 2 or 3 on question 10 suggests there is a suicidality risk.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Age greater than or equal to 18 years old.

  2. Mothers of infants ≤365 days of age admitted to the acute care floors at Texas Children's Hospital Medical Center Campus and their infant based on date of birth in Epic.

  3. English or Spanish speaking mother.

  4. Willing and able to provide informed consent.

  5. Mothers with Edinburgh Postpartum Depression Scale (EPDS) score more than or equal to 10

  6. Ability to complete study protocol.

NOTE: Inclusion item # 3 is as per their choice for bilingual mothers.

Exclusion Criteria:
  1. Mother and infant(s) reside outside 50-mile radius of Texas Children's Hospital Medical Center Campus based on address on demographic form.

  2. Mother is not the primary caregiver of infant(s) confirmed at time of informed consent.

  3. Enrollment in this study during previous hospitalization based on duplicate identified in database.

  4. Currently under care of psychiatrist or psychologist as reported in screening questionnaire.

NOTE: Exclusion item #2 is self-reported by the mothers at the time of screening for eligibility for the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Texas Children's Hospital - Women's Pavilion Houston Texas United States 77030
2 Texas Children's Hospital Houston Texas United States 77030

Sponsors and Collaborators

  • Michelle Lopez

Investigators

  • Principal Investigator: Michelle Lopez, MD, Texas Children's Hospital/Baylor College of Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michelle Lopez, Principal Investigator, Baylor College of Medicine
ClinicalTrials.gov Identifier:
NCT03777046
Other Study ID Numbers:
  • H44040
First Posted:
Dec 17, 2018
Last Update Posted:
Feb 8, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Michelle Lopez, Principal Investigator, Baylor College of Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 8, 2021