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Recruiting NCT06785467

eDoula Feasibility and Acceptability

No phase Interventional Pregnancy Related

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: eDoula App.
Who it may be relevant to
Registry conditions: Pregnancy Related. Basic parameters: 18 years — 50 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

eDoula: The Feasibility and Acceptability of Mobile Application in Pregnancy, Labor, and Birth Support

Overview

eDoula is an app that will give patients reading material and videos to watch based on their due date. It also provides helpful postpartum guidance. First, patients without access to the app will be recruited and surveyed on their labor and satisfaction outcomes. Then, recruitment will begin for the intervention arm of the study. Participants will be recruited to use the app and complete a survey during the postpartum period.

Interventions

  • Other eDoula App
    eDoula is an app that will give patients reading material and videos to watch based on their due date. It also provides helpful postpartum device.

Primary outcome measures

  • Satisfaction with eDoula app [Time frame: Measured in the 7 days following delivery]
  • eDoula App Use [Time frame: Recruitment (19-28 weeks gestation) to delivery]
Secondary outcome measures (3)
  • Labor Agentry Scale-10 (LAS-10) [Time frame: Measured in the 7 days following delivery]
  • Birth Satisfaction Scale-Revised (BSS-R) [Time frame: Measured in the 7 days following delivery]
  • Edinburgh Postnatal Depression Scale (EPDS) [Time frame: Measured in the 7 days following delivery]

Eligibility criteria

Inclusion criteria

  • Nulliparous
  • Singleton pregnancy
  • English speaking
  • Own a smart phone or other device capable of downloading and running the eDoula app
  • Delivered at 36 weeks 0 days gestation or later
  • Able to labor

Exclusion criteria

  • Planned cesarean delivery
  • Pregnancy complications including placenta accreta spectrum, vasa previa, intrauterine fetal demise, or known major fetal anomaly
  • Delivery planned at a location other than Oregon Health and Science University

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Sequential
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • Oregon Health & Science University — Portland

Identifiers

NCT: NCT06785467 · OHSU IRB 27596

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗