eDoula Feasibility and Acceptability

NCT ID: NCT06785467

Last Updated: 2025-04-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-23

Study Completion Date

2026-06-30

Brief Summary

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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.

Detailed Description

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Conditions

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Pregnancy Related

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SEQUENTIAL

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.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

No masking

Study Groups

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Control

These participants will receive routine pregnancy and delivery care.

Group Type NO_INTERVENTION

No interventions assigned to this group

eDoula Intervention

These participants will have access to the eDoula app during pregnancy.

Group Type EXPERIMENTAL

eDoula App

Intervention Type OTHER

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.

Interventions

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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.

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Oregon Health and Science University

OTHER

Sponsor Role lead

Responsible Party

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Fei Cai

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Fei Cai, MD

Role: PRINCIPAL_INVESTIGATOR

Oregon Health and Science University

Locations

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Oregon Health & Science University

Portland, Oregon, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Women's Health Research Unit Department of Ob/Gyn

Role: CONTACT

503-494-3666

Facility Contacts

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Women's Health Research Unit

Role: primary

503-494-3666

Other Identifiers

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OHSU IRB 27596

Identifier Type: -

Identifier Source: org_study_id

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