Can a home tablet catch wound infections before they send patients back to the hospital?
NCT ID NCT02767011
First seen Sep 09, 2026 · Last updated Sep 10, 2026 · Updated 1 time
Summary
Researchers are testing whether a home telehealth system can prevent complications after vascular surgery that involves a groin incision. Patients scheduled for these procedures are randomly assigned to receive either standard discharge instructions or a tablet with a weight scale, blood pressure cuff and blood glucose meter that sends readings to care managers. The care managers watch for warning signs and contact patients when alerts arise. The trial follows patients for 30 days to track hospital readmissions, wound infections and changes in quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Tele-Health Electronic Monitoring (THEM), a home tablet and sensor system that sends weight, blood pressure and blood sugar readings to care managers
- What this could lead to
- If it works, remote monitoring could help surgeons catch wound infections and other complications early, reducing hospital readmissions after groin vascular surgery.
- What could go wrong
- This is a small study of 30 patients at one center, so results may not apply broadly. Telehealth monitoring also depends on reliable internet or cell coverage, which some patients lack.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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30 people
The number who actually took part.
- Start date
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Jul 2016
- Finished
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Jul 2017
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1\. Patients with any planned vascular procedures with cut-down access to the groin and treated by one of the Charleston Area Medical Center -Vascular Surgeons in the Vascular Center (VCOE) will be consented and enrolled. Exclusion Criteria: 1. do not plan to do follow-up visit at the VCOE; 2. history of dementia; 3. do not have home internet service with WIFI or live outside of the provided cell coverage area (cell coverage will be provided for patients without internet WIFI).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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