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Not yet recruiting Not applicable NCT07408557

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

No applicable phase (e.g. observational)
Conditions: Childbirth Problems

Sponsor: Stanford University

trial.available_in: БГ
Overview
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).
Who can participate
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
Interventions
A digital application - Postpartum Companion
DEVICE
Locations 1
United States (1)
Lucille Packard Childrens Hospital
Palo Alto , California
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Female only
Minimum age
18 Years
Healthy volunteers
No
Start date
01.07.2026
Completion date
01.07.2027
Registry ID
NCT07408557
Source
clinicaltrials.gov
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