Short-term Telehealth Follow up After Hospital Discharge for Chronic Obstructive Pulmonary Disease Exacerbation

NCT01489241 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 155

Last updated 2015-02-24

No results posted yet for this study

Summary

The purpose of this study is to evaluate whether the introduction of a short-term telemonitoring program for chronic obstructive pulmonary disease (COPD) patients discharged from the hospital after disease exacerbation produces benefits in terms of a reduction in hospital readmissions and health related quality of life. In addition the trials evaluate the economical and organisational impact of the services and examine their acceptability by patients and health professionals.

Conditions

  • Pulmonary Disease, Chronic Obstructive

Interventions

PROCEDURE

Telemonitoring

Within 24 hours after patient's discharge, the telemedicine equipment is installed at the patient's home and patients are trained in the use of the equipment. Patients are followed by a dedicated telehealth centre. Patients at home are asked to fill out each morning the CAT questionnaire and to record extra use of COPD relief medications. Patients in stable conditions perform telespirometry and teleoximetry at 4 and 12 weeks. When a clinical worsening is detected (increase in CAT score by 5 points or higher on two consecutive days) the patient is contacted and asked to perform ad hoc telespirometry and teleoximetry and to send the data to the telehealth centre.

Sponsors & Collaborators

  • Ministry for Health and Social Solidarity, Greece

    collaborator OTHER
  • Municipality of Trikala, Greece

    collaborator OTHER
  • e-Trikala S.A.

    collaborator INDUSTRY
  • Cities Net SA

    collaborator INDUSTRY
  • Institute of Biomedical Research & Technology, Larissa, Greece

    collaborator OTHER
  • Institute of Communications and Computer Systems, Athens, Greece

    collaborator OTHER
  • Alexander Technological Educational Institute, Thessaloniki, Greece

    collaborator OTHER
  • University of Macedonia, Thessaloniki, Greece

    collaborator OTHER
  • University of Thessaly

    collaborator OTHER
  • Regional Health Authority of Sterea & Thessaly

    lead OTHER_GOV

Principal Investigators

  • Konstantinos Gourgoulianis, MD, PhD · Pulmonary Department - University Hospital of Larisa

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2013-11-30
Completion
2014-01-31

Countries

  • Greece

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01489241 on ClinicalTrials.gov