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eDoula Feasibility and Acceptability

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

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06785467
Enrollment
60
Registered
2025-01-21
Start date
2025-01-23
Completion date
2026-06-30
Last updated
2025-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy Related

Keywords

Labor, Birth

Brief summary

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

OTHEReDoula 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.

Sponsors

Oregon Health and Science University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Masking description

No masking

Intervention model description

Control group will receive routine care and will be recruited postpartum to respond to a survey on their labor and satisfaction outcomes. Once control group recruitment is complete, intervention recruitment will begin. Intervention arm participants will gain access to the eDoula app during pregnancy.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Satisfaction with eDoula appMeasured in the 7 days following deliveryParticipant-reported satisfaction with the eDoula app using a 3-question Likert scale. Scores can have a value from 3 to 15, with a higher score indicating greater satisfaction.
eDoula App UseRecruitment (19-28 weeks gestation) to deliveryThe number of days during pregnancy that the eDoula app was used

Secondary

MeasureTime frameDescription
Labor Agentry Scale-10 (LAS-10)Measured in the 7 days following deliveryInstrument measuring patient control during childbirth. Scores can have a value from 10 to 70, with a higher score indicating a better outcome.
Birth Satisfaction Scale-Revised (BSS-R)Measured in the 7 days following deliveryInstrument measuring patient satisfaction with the birth experience. Scores can have a value from 0 to 40, with higher scores representing greater birth satisfaction.
Edinburgh Postnatal Depression Scale (EPDS)Measured in the 7 days following deliveryInstrument measuring postnatal depression symptoms following delivery. Scores can have a falue from 0 to 30, with higher scores representing more symptoms of postnatal depression.

Countries

United States

Contacts

Primary ContactWomen's Health Research Unit Department of Ob/Gyn
whru@ohsu.edu503-494-3666

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026