KT(KT Corporation)-SNUBH(Seoul National University Bundang Hospital) U-health Cooperative Research

March 10, 2015 updated by: Chan-Yeong Heo

KT-SNUBH U-health Cooperative Research: Target Selection and Consumers' Intention Research for Commercialization of the Pressure Ulcer Management u-Health Solution

The purpose of this study is to analyse utility and compatibility of U-health solution service based on mobile for chronic wound management.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

In this study, 'the management of pressure ulcer' defined as procedures comprising wound assessment, wound dressing and infection control, visually evaluated the outcomes of 'the management of pressure ulcer' through the tele-consultation.

This study designed to draw service targets based on utility and compatibility of U-health solution service and to analyse whether health providers use U-health solution service.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Korea, Republic of
    • Gyeonggi-do
      • Seongnam-si, Gyeonggi-do, Korea, Republic of, 463-707
        • Seoul National University Bundang Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

21 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Subject who has pressure ulcer or Health care provider for wound management

Exclusion Criteria:

  • Subject who have Osteomyelitis
  • Subject who have suppuration
  • Subject who participated in other clinical trial within 30 days from screening date

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Tele-consultation system
compare the Live assessed wound size with the transmitted Smart phone-based wound size through Tele-consultation system
Device: Smart phone
  • measure the Live assessed wound size and the transmitted Smart phone-based wound size
  • determine dressing materials using Smart phone-based tele-consultation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
concordance rate of wound size between live assessed wound size and transmitted wound size
Time Frame: a week from post treatment
a week from post treatment

Secondary Outcome Measures

Outcome Measure
Time Frame
concordance rate of wound size between live assessed wound size and transmitted wound size
Time Frame: 2 weeks from post treatment
2 weeks from post treatment
concordance rate of wound size between live assessed wound size and transmitted wound size
Time Frame: 3 weeks from post treatment
3 weeks from post treatment
concordance rate of wound size between live assessed wound size and transmitted wound size
Time Frame: 4 weeks from post treatment
4 weeks from post treatment

Other Outcome Measures

Outcome Measure
Time Frame
Satisfaction degree of the tele-consultation as measured by questionnaire.
Time Frame: 4 weeks from post treatment
4 weeks from post treatment
Usability survey
Time Frame: 4 weeks from post treatment
4 weeks from post treatment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Chan-Yeong Heo

Collaborators

KT Corporation

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2012

Primary Completion (Actual)

December 1, 2012

Study Completion (Actual)

January 1, 2013

Study Registration Dates

First Submitted

March 3, 2015

First Submitted That Met QC Criteria

March 10, 2015

First Posted (Estimate)

March 11, 2015

Study Record Updates

Last Update Posted (Estimate)

March 11, 2015

Last Update Submitted That Met QC Criteria

March 10, 2015

Last Verified

March 1, 2015

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • E-1206/158-001

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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