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

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorStanford University

About this trial

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).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Able to speak, read and understand English

Delivered a live infant

18 years old or older

Disqualifiers

Fetal demise / infant death

Refusal to participate

Less than 18 years old

Unable to provide informed consent

Trial design

Design model

Single group

Treatments tested in this trial

  • A digital application - Postpartum Companion

    Device

    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.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Digital application - Postpartum CompanionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The number of participants that used the digital application

Participant engagement will be measured by the proportion of patients who used the tool

Time frame
From time of enrollment to up to 12 weeks postpartum

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: