CClinicalTrials.gg
Not yet recruitingNCT07408557STORKUpdated Apr 21, 2026

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

An interventional study of A digital application - Postpartum Companion in Childbirth Problems, sponsored by Stanford University. Not yet recruiting at 1 site in United States. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-21.

Sponsored by Stanford University · Not applicable, Interventional, and Other

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years and older
Sex
Female
01

Study 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).
02

Conditions studied

  • Childbirth Problems
03

In context

Lead sponsor

Stanford University is the lead sponsor of 2,117 studies on the registry; 425 are open to participants now.

Of its 259 completed or terminated interventional studies of FDA-regulated products, 197 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

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
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Digital application - Postpartum Companion

    Participants will be asked to download the digital application to evaluate postpartum recovery and provide informational resources after childbirth for 12 weeks.

    Device: A digital application - Postpartum Companion

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.

06

What researchers measure

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

07

Study locations

1 site
  • Lucille Packard Childrens Hospital
    Palo Alto, California 94305, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07408557
Lead sponsor
Stanford University
Responsible party
Gillian Hilton (Professor, Dept of Anesthesiology, Stanford University) — Principal investigator
First posted
Feb 13, 2026
Start date
Jul 2026 (estimated)
Primary completion
Mar 2027 (estimated)
Completion
Jul 2027 (estimated)
Last update
Apr 21, 2026

Study contacts

Gillian Abir, MBBS
principal investigator · Stanford University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion