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Research to Evaluate Efficiency in U-health Solution Service for the Chronic Wound Management

A Smart Phone-based Tele-consultation System in the Management of Chronic Pressure Ulcer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02382302
Enrollment
20
Registered
2015-03-06
Start date
2011-07-31
Completion date
2012-02-29
Last updated
2015-03-06

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

Conditions

Pressure Ulcer

Keywords

U-health, chronic wound management

Brief summary

This trial is a prospective research to evaluate efficiency in U-health solution service based on Mobile for the chronic wound management.

Detailed description

This trial conducted to assess the efficiency of teleconsultation using the smart-phone-based store-and-forward system in promoting the wound healing process as well as cost-effectiveness in patients with pressure ulcer.

Interventions

The data such as photographs can be collected simply using built-in cameras installed in smart-phones that used the standard touch-screen user interface (UI) and camera installed in the iPhone3GS and iPhone4 using iOS 3.0 and iOS 5.0, respectively. Subjects were instructed to transmit the photographs of the wounds then investigator performed the photography in such a manner that the size of pressure ulcer should be automatically measured based on a 1 cm x 1 cm-sized indicator on the screen.

Sponsors

KT Corporation
CollaboratorINDUSTRY
Chan-Yeong Heo
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subjects who have pressure ulcer * Subjects who voluntarily decided the participation of the study and signed the informed consent

Exclusion criteria

* Subjects who have Osteomyelitis * Subjects who have suppuration * Subjects who participated in other clinical trial within 30 days from screening date

Design outcomes

Primary

MeasureTime frameDescription
Concordance rate for the wound and the type of dressing on the Pressure Sore Status Tool (PSST)4weeks post-treatment1. Data collection * The measurement of the size of pressure ulcer * Medical examination;the degree of recovery of pressure ulcer 2. Remote physician monitoring \- The patient data was transmitted from the smart-phone to the website via open application programming interface (API) 3. Prescription 4. Data analysis - One plastic surgeon, one Wound Ostomy Continence Nurse(WOCN) and one researcher grossly examined the wound sites of each patient and assessed the pressure ulcer using the revised PSST based on a 4-6 point scale.

Secondary

MeasureTime frameDescription
Concordance rate for the wound and the type of dressing on the Pressure Sore Status Tool (PSST)1week post-treatment1. Data collection * The measurement of the size of pressure ulcer * Medical examination;the degree of recovery of pressure ulcer 2. Remote physician monitoring \- The patient data was transmitted from the smart-phone to the website via open application programming interface (API) 3. Prescription 4. Data analysis - One plastic surgeon, one Wound Ostomy Continence Nurse(WOCN) and one researcher grossly examined the wound sites of each patient and assessed the pressure ulcer using the revised PSST based on a 4-6 point scale.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026