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Internet-delivered Postpartum Anxiety Prevention (PPOD)

West Virginia University logo

West Virginia University

Status

Completed

Conditions

Postpartum Disorder

Treatments

Behavioral: P-POD

Study type

Interventional

Funder types

Other

Identifiers

NCT03563339
1710795361

Details and patient eligibility

About

Postpartum anxiety disorders are the most prevalent postpartum psychiatric conditions. Up to 16% of mothers experience postpartum anxiety or related disorders, such as OCD. With respect to the investigator's own community, this means that up to 3,313 women in West Virginia may struggle with postpartum anxiety or OCD. Left untreated, perinatal anxiety and OCD are associated with numerous adverse outcomes, such as maternal depression, preterm birth, impaired fetal development, low birthweight, difficulty breastfeeding, anxiety in children, and interference with parent-infant bonding. Critically, anxiety is a risk factor for cardiovascular disease and substance use disorders, both significant West Virginia health disparities. Thus, there is a critical need to develop effective and scalable prevention programs to address postpartum anxiety and OCD. The purpose of this proposed community-engaged study is to develop and test the feasibility, usability, and acceptability of an Internet-delivered postpartum anxiety and OCD prevention program, called "Preventing Postpartum Onset Distress", or P-POD.

Enrollment

19 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female
  • Aged 18 or older
  • Pregnant with first child
  • Married or living with a partner
  • State Trait Anxiety Inventory-Trait Total ≥ 44 and/or Obsessive Beliefs Questionnaire-44 Total ≥ 139

Exclusion criteria

  • past or current anxiety disorders
  • past or current OCD
  • past or current psychotic disorders
  • past or current bipolar disorders
  • past or current substance use disorders.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

19 participants in 1 patient group

P-POD
Experimental group
Description:
All participants will complete the prevention for postpartum onset distress (P-POD)
Treatment:
Behavioral: P-POD

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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