Engage & Connect: A Psychotherapy for Postpartum Depression
Launched by WEILL MEDICAL COLLEGE OF CORNELL UNIVERSITY · Oct 14, 2022
Trial Information
Current as of July 23, 2025
Recruiting
Keywords
ClinConnect Summary
The "Engage & Connect" clinical trial is studying a new type of therapy designed to help women who are experiencing postpartum depression, which is depression that can occur after having a baby. This trial will compare the new therapy, called Engage & Connect, with another supportive program that focuses on reviewing symptoms and providing education about postpartum depression. The study lasts for 9 weeks and is conducted online, so participants can join from home. Researchers want to see how this therapy affects feelings of social isolation, the ability to enjoy social interactions, and the severity of depression.
To be eligible for this trial, women must be within a year of giving birth and have a specific score indicating postpartum depression. They should either not be taking antidepressants or be on a stable dose for at least 8 weeks. It's important that participants are able to speak English and can give consent to take part in the study. However, the trial cannot include those who are currently suicidal, in ongoing therapy, or have certain serious mental health issues. If you join, you can expect to engage in a supportive program that aims to improve your mental well-being over the treatment period.
Gender
FEMALE
Eligibility criteria
- Inclusion Criteria:
- • 1. Up to 1 year post-delivery
- • 2. Edinburgh Postnatal Depression Scale (EPDS) score ≥ 10.
- • 3. Off antidepressants or on a stable dose of an antidepressant for 8 weeks and do not intend to change the dose in the next 10 weeks.
- • 4. Capacity to provide consent for research assessment and treatment.
- • 5. Speaks English proficiently
- Exclusion Criteria:
- • 1. Intent or plan to attempt suicide in the near future
- • 2. Ongoing psychotherapy (no more than once every 8 weeks or during the duration of the intervention)
- • 3. Active substance abuse or dependence
- • 4. Severe fetal anomalies, stillbirth or infant death at time of enrollment for index pregnancy
- • 5. History or presence of psychiatric diagnoses other than major depressive disorder without psychotic features, generalized anxiety disorder, persistent depressive disorder, or specific phobia.
- • 6. Use of psychotropic drugs or cholinesterase inhibitors other than use of ≤ 0.5 mg of lorazepam daily up to seven times per week.
About Weill Medical College Of Cornell University
Weill Medical College of Cornell University is a leading academic institution dedicated to advancing medical research and education. As a prominent sponsor of clinical trials, it focuses on innovative healthcare solutions and the development of new therapies across various medical disciplines. The institution is committed to fostering collaborative research efforts that enhance patient care and improve health outcomes. With a robust infrastructure and a team of experienced researchers and clinicians, Weill Cornell aims to translate scientific discoveries into practical applications, ensuring a strong emphasis on ethical standards and regulatory compliance throughout the clinical trial process.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New York, New York, United States
Patients applied
Trial Officials
Nili Solomonov, PhD
Principal Investigator
Weill Medical College of Cornell University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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