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Testing of Mobile Monitoring System

Stanford University logo

Stanford University

Status

Not yet enrolling

Conditions

Orthopedic Disorder

Treatments

Behavioral: Mobile Monitoring Tool

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Orthopaedic surgery patient at hospital 175

Exclusion criteria

  • no access to mobile phone

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

500 participants in 1 patient group

Mobile monitoring group
Experimental group
Treatment:
Behavioral: Mobile Monitoring Tool

Trial contacts and locations

0

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Central trial contact

Sara Kemper

Data sourced from clinicaltrials.gov

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