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Adapting the Stanford Obstetric Recovery Checklist in Postpartum Women to a Digital Health Platform: A Feasibility Study

Adapting the Stanford Obstetric Recovery Checklist (STORK) to a Digital Health Platform: A Feasibility and User Feedback Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07408557
Acronym
STORK
Enrollment
60
Registered
2026-02-13
Start date
2026-07-01
Completion date
2027-07-01
Last updated
2026-04-21

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

Conditions

Childbirth Problems

Brief summary

Explore patient experiences engaging with a digital tool (app- and web-based) to support postpartum recovery. Postpartum recovery involves physical, emotional, and social changes, and many patients report unmet needs for timely guidance and reassurance. Digital health applications may provide scalable support by collecting patient-reported wellbeing data and delivering tailored education and self-management guidance. However, patient experience, acceptability, perceived usefulness require evaluation to inform implementation and improvements. Primary objective • To evaluate patient experience using the postpartum recovery app, including acceptability, usability, and perceived usefulness for the first 12 weeks postpartum. Secondary objectives * To characterize how patients engage with app content over time. * To gather patient recommendations for content and wording. * To evaluate patient engagement with the app over first 12 weeks postpartum (frequency and duration of use).

Interventions

DEVICEA digital application - Postpartum Companion

This is an application that provides mixed media resources to support postpartum mothers, including videos and articles about how to manage postpartum recovery (physical, social, and mental well being). Participants will be able to use the application beyond the follow up end point of 12 weeks. Data will be collected up to 12 weeks postpartum.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

This is an explorative study evaluating patient engagement and feedback on a digital tool to support postpartum recovery.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Able to speak, read and understand English * Delivered a live infant * 18 years old or older

Exclusion criteria

* Fetal demise / infant death * Refusal to participate * Less than 18 years old * Unable to provide informed consent * Unable to speak, read and/or understand English * No access to a suitable device to use the digital tool

Design outcomes

Primary

MeasureTime frameDescription
The number of participants that used the digital applicationFrom time of enrollment to up to 12 weeks postpartumParticipant engagement will be measured by the proportion of patients who used the tool

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORGillian Abir, MBBS

Stanford University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 22, 2026