Testing of Mobile Monitoring System

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

Status

Withdrawn

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04601376

Enrollment

Registered

2020-10-23

Start date

2027-02-01

Completion date

2028-12-01

Last updated

2026-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Orthopedic Disorder

Brief summary

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

Interventions

BEHAVIORALMobile Monitoring Tool

a text-messaged based outcomes collection system

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Orthopaedic surgery patient at hospital 175

Exclusion criteria

* no access to mobile phone

Design outcomes

Primary

Measure	Time frame	Description
Promis PF Short form (change in self reported capability)	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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026