To Implement and Test the Mobile Monitoring Tool to Identify SSI (R33 Phase)

Stanford University0 sites500 target enrollmentDecember 2025

ConditionsOrthopedic Disorder

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Orthopedic Disorder
Sponsor: Stanford University
Enrollment: 500
Primary Endpoint: Promis PF Short form (change in self reported capability)
Status: Not yet recruiting
Last Updated: last year

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

We will complete a prospective, observational study comparing the accuracy of the mobile monitoring tool on identifying SSI compared to manual review.

Registry

clinicaltrials.gov

Start Date

December 2025

End Date

December 2026

Last Updated

last year

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

Stanford University

Responsible Party

Principal Investigator

Robin Kamal

Assistant Professor

Stanford University

Eligibility Criteria

Inclusion Criteria

•Orthopaedic surgery patient at hospital 175

Exclusion Criteria

•no access to mobile phone

Outcomes

Primary Outcomes

Promis PF Short form (change in self reported capability)

Time Frame: 1 day, 1 week, 2 week, 4 week, 12 weeks after surgery

PROMIS Physical Function instruments measure self-reported capability rather than actual performance of physical activities. It is scored from 0-100, a higher score indicates better physical function