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Completed

NCT Number: NCT02385942

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

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

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Key information

Conditions

Pressure Ulcer Skin Diseases Skin Ulcer Skin and Connective Tissue Diseases

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, 463-707, South Korea

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Smart phone

Device
  • measure the Live assessed wound size and the transmitted Smart phone-based wound size
  • determine dressing materials using Smart phone-based tele-consultation

Primary outcomes

  1. concordance rate of wound size between live assessed wound size and transmitted wound size

    Time frame: a week from post treatment

Secondary outcomes

  1. concordance rate of wound size between live assessed wound size and transmitted wound size

    Time frame: 2 weeks from post treatment

  2. concordance rate of wound size between live assessed wound size and transmitted wound size

    Time frame: 3 weeks from post treatment

  3. concordance rate of wound size between live assessed wound size and transmitted wound size

    Time frame: 4 weeks from post treatment

Other outcomes

  1. Satisfaction degree of the tele-consultation as measured by questionnaire.

    Time frame: 4 weeks from post treatment

  2. Usability survey

    Time frame: 4 weeks from post treatment

Sponsors and collaborators

Lead sponsor

Chan-Yeong Heo

Other

Collaborators

  • KT Corporation

Registry information

Official study title

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

Important dates

Study start
2012
Primary completion
2012
Study completion
2013
First posted
Mar 11, 2015
Registry last updated
Mar 11, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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