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Recruiting NCT06991166

NCT06991166 OBWELL: Innovative Psychotherapeutic Intervention to Treat Postpartum Depression

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Clinical Trial Summary
NCT ID NCT06991166
Status Recruiting
Phase
Sponsor Hackensack Meridian Health
Condition Post Partum Depression
Study Type INTERVENTIONAL
Enrollment 72 participants
Start Date 2025-09-15
Primary Completion 2028-09-01

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Cognitive behavioral therapy (CBT) psychotherapy group/telehealthInterpersonal therapy (IPT) psychotherapy group/telehealth

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 72 participants in total. It began in 2025-09-15 with a primary completion date of 2028-09-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Postpartum Depression (PPD) is defined as depression that occurs after childbirth, with intense symptoms that last longer than "baby blues". PPD differs greatly from "baby blues", a term used to describe the typical sadness, worry and tiredness that women experience after childbirth, which often resolves within a week or two on its own. The symptoms of PPD interfere with many aspects of daily living and can have unhealthy short-term and long-term outcomes, both for the mother and baby. One-third of women in the U.S. with PPD are identified in clinical settings, yet only half of those begin psychotherapy treatment. Unfortunately, mothers whose newborns are in the Neonatal Intensive Care Unit (NICU) are at high risk for developing PPD, necessitating early identification and evidence-based treatment. Cognitive behavioral therapy (CBT) and interpersonal therapy (IPT) are the two most effective psychotherapy treatments for PPD, yet no randomized controlled clinical trials were found that directly compared the two types of treatment or determined whether combining the two approaches is more helpful for PPD than either approach alone. This clinical trial aims to compare the effectiveness of a 4-week intervention of either CBT or IPT for PPD in NICU mothers and to determine whether a sequential 8-week intervention (IPT then CBT, or CBT then IPT) is more beneficial.

Eligibility Criteria

Inclusion Criteria: * Mother of NICU infant * Older than age 18 * English-speaking * Gave birth more than 24 hours ago and less than 12 months prior to enrollment * Depression as assessed by: Current/Prior diagnosis of Major Depressive Disorder OR EPDS score above 10 OR EPDS score below 10 AND Endorsement of "sometimes" or "often" on item #10 on the EPDS\* ("I have had thoughts of harming myself") Exclusion Criteria: * A diagnosis of Substance Dependency or Substance Use * Acute suicidal or infanticidal ideation * Current psychosis * Medical history of cognitive impairment * Infant death of current NICU admission * Marked non-compliance with intervention (e.g, non-attendance of more than one session during a 4-week intervention or failure to complete study assessments), * Are in medical treatment that would prevent participation (i.e., medical treatment that requires inpatient hospitalization and thus would prevent participation of study visits.)

Contact & Investigator

Central Contact

Melissa Giuliano, LMSW

✉ Melissa.Giuliano@hmhn.org

📞 5519964450

Principal Investigator

Yeraz Markarian, PhD

PRINCIPAL INVESTIGATOR

Hackensack Meridian Health

Frequently Asked Questions

Who can join the NCT06991166 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Post Partum Depression. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06991166 currently recruiting?

Yes, NCT06991166 is actively recruiting participants. Contact the research team at Melissa.Giuliano@hmhn.org for enrollment information.

Where is the NCT06991166 trial being conducted?

This trial is being conducted at Hackensack, United States.

Who is sponsoring the NCT06991166 clinical trial?

NCT06991166 is sponsored by Hackensack Meridian Health. The principal investigator is Yeraz Markarian, PhD at Hackensack Meridian Health. The trial plans to enroll 72 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology