Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05772897 · ClinicalTrials.gov registry record · NA

Parenting Skills Group for Mothers With Postpartum Depression

A NA study of Postpartum Depression, sponsored by University of Colorado, Denver.

Recruiting
Registry status
NA
Development phase
750
Enrollment target
1
Study location

NCT05772897: Recruiting NA study of Postpartum Depression, sponsored by University of Colorado, Denver.

NCT05772897 is a NA study of Postpartum Depression that is actively recruiting participants, run by University of Colorado, Denver. The registered enrollment target is 750 participants, above the 459-participant average among 47 other Postpartum Depression trials with a reported enrollment target (63% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05772897, a NA study of Postpartum Depression, is actively recruiting participants, sponsored by University of Colorado, Denver.

RECRUITING
Registry status
NA
Development phase
750 participants
Enrollment target
1
Study location

Study Summary

The goal of this longitudinal study is to study the effects of a parenting skills group (Circle of Security Parenting, aka COSP) in mothers with postpartum depression. The main questions it aims to answer are: * Will changes in methylation of the OXTR rs53576 be apparent in mother and/or infant after having gone through the 8-week COSP program? * Will COSP participation be associated with improved symptoms of postpartum depression (over and above standard care), attachment style, and relational characteristics of the mother-infant dyad? * Will COSP participation be associated with changes in social behavior in the infant, and if so, do they persist throughout childhood? Participants will * Participate in an 8-week COSP program delivered remotely via Zoom. * Provide buccal swabs (mother and infant) to assess changes in methylation of OXTR rs53576 pre- versus post-intervention. * Complete a series of assessment questionnaires delivered remotely. * Videotape a play-based assessment in their home. * Receive infant developmental testing Researchers will compare characteristics of waitlist controls to those participating in the COSP program at the mid-way point of the program to see if the two groups differ.

Primary Outcome

Buccal swabs from mother and infant

Conditions Studied

Interventions

  • BEHAVIORAL Circle of Security Parenting program

Study Locations (1)

Colorado

  • University of Colorado Denver - Denver

Trial Details

FieldValue
Enrollment Target 750 participants
Start Date 2023-08-03
Est. Completion 2035-06-01
Phase NA
University of Colorado, Denver

1,283 total trials

What NCT05772897 shows while recruiting

NCT05772897 is an interventional study that assigns participants to a tested intervention. The registered 750 participants enrollment target is mid-sized for trials with a published cap, above the 459-participant average among 47 other Postpartum Depression trials with a reported enrollment target (63% higher).

The record links to 1 condition, with Postpartum Depression appearing as the primary indexed condition, and to 1 intervention - of which Circle of Security Parenting program is the first listed.

NCT05772897 reports a single indexed study location in Colorado.

Frequently Asked Questions

What is clinical trial NCT05772897 about?

NCT05772897 is a clinical study titled "Parenting Skills Group for Mothers With Postpartum Depression". The goal of this longitudinal study is to study the effects of a parenting skills group (Circle of Security Parenting, aka COSP) in mothers with postpartum depression. The main questions it aims to answer are: * Will changes in methylation of the OXTR rs53576 be apparent in mother and/or infant aft...

What is the current status of trial NCT05772897?

This trial is currently recruiting. It is a NA study. The enrollment target is 750 participants. The study started on 2023-08-03. Estimated completion is 2035-06-01.

What conditions does trial NCT05772897 study?

This clinical trial studies the following conditions: Postpartum Depression.

What interventions are being tested in trial NCT05772897?

The interventions under investigation include: Circle of Security Parenting program (BEHAVIORAL).

Who is sponsoring clinical trial NCT05772897?

This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05772897 being conducted?

This trial has 1 study location across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Postpartum Depression

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05772897's enrollment target sits among peer trials

750 5th of 47 higher than 42 of 47 other Postpartum Depression trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Postpartum Depression trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02048332 · 750 participants · Phase 1

    Donor-Derived Viral Specific T-cells (VSTs)

  • NCT02087852 · 750 participants

    Kidney Cancer DNA Registry

  • NCT02532452 · 750 participants · Phase 2

    Third Party Viral Specific T-cells (VSTs)

  • NCT03126916 · 750 participants · Phase 3

    Testing the Addition of 131I-MIBG or Lorlatinib to Intensive Therapy in People With High-Risk Neuroblastoma (NBL)

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05772897, the US trial registry maintained by the National Library of Medicine. NCT05772897 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.