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NCT06208852 · ClinicalTrials.gov registry record · NA

Virtual Patient Navigation During a Pandemic

A NA study of Post Partum Depression, sponsored by Children's Hospital of Philadelphia.

Recruiting
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT06208852 is a NA study of Post Partum Depression that is actively recruiting participants, run by Children's Hospital of Philadelphia. The registered enrollment target is 40 participants, below the 231-participant average among 9 other Post Partum Depression trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06208852, a NA study of Post Partum Depression, is actively recruiting participants, sponsored by Children's Hospital of Philadelphia.

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

Study Summary

The sub-study will involve a rigorous mixed-methods design. The qualitative phase of the sub-study will consist of semi-structured interviews. During the semi-structured interviews, 10 eligible women will be recruited to identify barriers and facilitators to accessing virtual mental health services. This information will be used to adapt an evidence-based patient navigation intervention for virtual use. For the intervention phase of the sub-study, 30 women with persistent postpartum depression symptoms will be recruited to participate in the adapted virtual navigator program using rapid cycle testing over a 2-month period.

Conditions Studied

Interventions

  • OTHER Virtual Navigator Program

Study Locations (1)

Pennsylvania

  • Children's Hospital of Philadelphia - Philadelphia

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2023-06-29
Est. Completion 2026-06
Phase NA

Sponsor

Children's Hospital of Philadelphia

431 total trials

What the Registry Record Tells You About NCT06208852

The ClinicalTrials.gov registry entry for NCT06208852 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 231-participant average among 9 other Post Partum Depression trials with a reported enrollment target (83% lower). The listed sponsor is Children's Hospital of Philadelphia, which has 431 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Post Partum Depression appearing as the primary indexed condition, and to 1 intervention - of which Virtual Navigator Program is the first listed.

NCT06208852 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT06208852 about?

NCT06208852 is a clinical study titled "Virtual Patient Navigation During a Pandemic". The sub-study will involve a rigorous mixed-methods design. The qualitative phase of the sub-study will consist of semi-structured interviews. During the semi-structured interviews, 10 eligible women will be recruited to identify barriers and facilitators to accessing virtual mental health services....

What is the current status of trial NCT06208852?

This trial is currently recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2023-06-29. Estimated completion is 2026-06.

What conditions does trial NCT06208852 study?

This clinical trial studies the following conditions: Post Partum Depression.

What interventions are being tested in trial NCT06208852?

The interventions under investigation include: Virtual Navigator Program (OTHER).

Who is sponsoring clinical trial NCT06208852?

This trial is sponsored by Children's Hospital of Philadelphia, which has 431 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06208852 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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