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P-POD for Postpartum Depression (PPOD Trial)

N/A
Waitlist Available
Research Sponsored by West Virginia University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline to week 10
Awards & highlights

PPOD Trial Summary

This study is evaluating whether an internet-delivered program can help reduce anxiety in new mothers.

Eligible Conditions
  • Postpartum Depression

PPOD Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline to week 10
This trial's timeline: 3 weeks for screening, Varies for treatment, and change from baseline to week 10 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Obsessive Beliefs Questionnaire (OBQ-44)
State-Trait Anxiety Inventory-Trait (STAI-Trait)

PPOD Trial Design

1Treatment groups
Experimental Treatment
Group I: P-PODExperimental Treatment1 Intervention
All participants will complete the prevention for postpartum onset distress (P-POD)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
P-POD
2020
N/A
~20

Find a Location

Who is running the clinical trial?

West Virginia UniversityLead Sponsor
176 Previous Clinical Trials
60,195 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Internet-delivered Postpartum Anxiety Prevention
Shari Steinman Haxel 2020. "Internet-delivered Postpartum Anxiety Prevention". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT03563339.
~4 spots leftby Apr 2025
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