RHCluster2GR: Life-long Tele-monitoring of Patients With Type 2 Diabetes Mellitus in Central Greece

Sponsor
Regional Health Authority of Sterea & Thessaly (Other)
Overall Status
Completed
CT.gov ID
NCT01498367
Collaborator
Ministry for Health and Social Solidarity, Greece (Other), Municipality of Trikala, Greece (Other), e-Trikala S.A. (Industry), Cities Net SA (Industry), Institute of Biomedical Research & Technology, Larissa, Greece (Other), Institute of Communications and Computer Systems, Athens, Greece (Other), Alexander Technological Educational Institute, Thessaloniki, Greece (Other), University of Macedonia, Thessaloniki, Greece (Other), University of Thessaly (Other)
154
1
2
34.1
4.5

Study Details

Study Description

Brief Summary

To evaluate whether patients with type 2 diabetes mellitus can be followed by simplified, centralized and large scale tele-monitoring of blood glucose levels and blood pressure, and whether this intervention produces health and economic benefits when introduced without major changes to the existing organization of a large tertiary care center.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Telemonitoring of patients with diabetes type 2
N/A

Detailed Description

The present study aims to examine the clinical and financial effects and the patients' perception and satisfaction of home telemedicine support system for diabetes management versus standard (usual) care. In the intervention group the patients will be provided with a blood glucose meter and a mobile phone and their data will be transferred via the mobile to the regional database and will be assessed by the allocated care team. Appropriate counseling on treatment and symptoms or problems related to diabetes will also be provided.

Measurements of HbA1c will be taken to assess glycaemic control while the dietary and the exercise habits will be assessed by the use of questionnaires. In addition the patients' satisfaction from the use of the telemedicine service will be studied. A Cost-Effective Analysis and Cost Utility Analysis will be applied to evaluate the tele-health service compared with the usual care from the health and social perspective. The effect of the tele-health service in the organization structure of the outpatient hospital department will be evaluated with a qualitative study.

Study Design

Study Type:
Interventional
Actual Enrollment :
154 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Renewing Health RCT for the Evaluation of Life-long Tele-monitoring of Patients With Diabetes Mellitus Type 2 in Central Greece
Study Start Date :
Mar 1, 2011
Actual Primary Completion Date :
Dec 1, 2013
Actual Study Completion Date :
Jan 1, 2014

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Usual care

Participants in the control group receive usual care. Usual care consists of regular visits to the specialist when required. In the occasion of the visit, HbA1c and glucose measurements are performed and the current oral or insulin therapy is modified if necessary. Patients also receive basic education in the management of diabetes.

Experimental: Telemonitoring of diabetes 2 patients

Patients will have one educational visit to set up the system and explain how it works. Patients will download their measurements from their tele-glucose meter to their mobile phone and the data will be transferred to the regional database. The care team (a nurse specially trained and the allocated physician) will regularly access the patient's home diary, and will provide the appropriate counselling and medication changes as frequently as necessary. In addition to blood glucose measurements, routine questions about symptoms and eventual difficulties related to diabetes as well as diabetic management will be routinely captured and reported.

Procedure: Telemonitoring of patients with diabetes type 2
Telemonitoring of the patients's blood glucose level measurements using a the tele-glucose meter

Outcome Measures

Primary Outcome Measures

  1. Health related quality of life of the patients measured by the SF-36 version 2 questionnaire [12 months minimum- at the entry point of the intervention and the end.]

  2. HbA1c levels [12 months minimum - at the entry point and every 3 months.]

    Glycated hemoglobin (HbA1c) levels at the entry point and every 3 months (for a period of 12 months minimum)

Secondary Outcome Measures

  1. Emotional functioning in diabetes assessed by the "Problem areas in diabetes questionnaire - PAID © 1999 Joslin Diabetes Center" [12 months minimum- at the entry point of the intervention and the end.]

  2. Physical activity measured by the "International Physical Activity Questionnaire" (IPAQ) [12 months minimum- at the entry point of the intervention and the end.]

  3. Nutrition habits assessed by validated questionnaire. [12 months minimum- at the entry point of the intervention and the end.]

  4. Patients' Acceptance-Satisfaction measured by the WSD Questionnaire [at 2nd and at 12th month]

  5. Economic Evaluation (Cost-Effective Analysis- Cost Utility Analysis) [12 months minimum]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of type 2 Diabetes

  • HbA1c > 53 mmol/mol (7.0 % according to NGSP)

  • Capability to use the devices provided

  • Being cognitively able to participate

  • Capability of filling in questionnaires in german or greek language

  • Absence of severe comorbidity prevalent on diabetes with life expectancy < 12 months

Exclusion Criteria:
  • Pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Endocrinology and Metabolic Diseases Department - Regional University Hospital of Larisa Larisa Thessaly Greece 41110

Sponsors and Collaborators

  • Regional Health Authority of Sterea & Thessaly
  • Ministry for Health and Social Solidarity, Greece
  • Municipality of Trikala, Greece
  • e-Trikala S.A.
  • Cities Net SA
  • Institute of Biomedical Research & Technology, Larissa, Greece
  • Institute of Communications and Computer Systems, Athens, Greece
  • Alexander Technological Educational Institute, Thessaloniki, Greece
  • University of Macedonia, Thessaloniki, Greece
  • University of Thessaly

Investigators

  • Principal Investigator: Georgios Koukoulis, MD, PhD, Endocrinology and Metabolic Diseases Department - Regional University Hospital of Larisa

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Georgios Koukoulis, Associate Proffesor, Director of the Endocrinology and Metabolic Diseases Department, University Hospital of Larissa, Regional Health Authority of Sterea & Thessaly
ClinicalTrials.gov Identifier:
NCT01498367
Other Study ID Numbers:
  • FR2015
  • EC Grant Agreement 250487
First Posted:
Dec 23, 2011
Last Update Posted:
Feb 18, 2015
Last Verified:
Feb 1, 2015
Keywords provided by Georgios Koukoulis, Associate Proffesor, Director of the Endocrinology and Metabolic Diseases Department, University Hospital of Larissa, Regional Health Authority of Sterea & Thessaly
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 18, 2015