TeLIPro Health Program - Active With Diabetes

Sponsor
West German Center of Diabetes and Health (Other)
Overall Status
Recruiting
CT.gov ID
NCT03675919
Collaborator
AOK Rhineland / Hamburg (Other), German Institute for Telemedicine and Health Promotion (Other), German Diabetes Center (Other)
2,018
1
2
47.5
42.4

Study Details

Study Description

Brief Summary

In a randomized-controlled trial the hypothesis should be tested that the Telemedical Lifestyle Intervention Program TeLIPro could significantly improve HbA1c (primary outcome), body weight and composition, cardiovascular risk factors, quality of life, eating behavior, and medication demand (secondary outcomes) in type 2 diabetes mellitus (T2DM) patients.

Condition or Disease Intervention/Treatment Phase
  • Device: Scale
  • Device: Step counter
  • Device: Blood glucose meter with test stripes
  • Other: Access to the online portal
  • Other: Telemedical coaching
N/A

Detailed Description

T2DM patients, assured at the health insurance AOK Rhineland / Hamburg will be randomized into two parallel groups. In addition to routine care both groups will be provided a scale as well as a step counter and access to a secured online portal. The TeLIPro group will additionally got a glucose meter with test stripes fpr self-monitoring of blood glucose and telemedical coaching.

Participants of both groups will enter their anthropometric and metabolic data into a database on quarterly basis. In addition, the costs for diabetes-specific treatment, inpatient and outpatient treatment costs and drug costs will be analyzed on the basis of the routine data of the AOK Rhineland / Hamburg.

Patient preference for type 2 diabetes intervention will be recorded using Discrete Choice Experiment (DCE) questionnaires at the beginning of the program and at the end of the intervention. As part of the development and validation of the DCE, focus groups are used to determine the DCE attributes. In addition, focus groups should also be used during the data collection in order to obtain additional information on patient preferences by means of qualitative analysis.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
2018 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
randomized controlled trialrandomized controlled trial
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
The Telemedical Lifestyle Intervention Program TeLIPro (TeLIPro Health Program - Active With Diabetes)
Actual Study Start Date :
Sep 15, 2018
Actual Primary Completion Date :
Sep 21, 2021
Anticipated Study Completion Date :
Sep 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Control group

The control group will be provided a scale, a step counter as well as access to the online portal and will remain in routine care.

Device: Scale
self-monitoring of body weight; with automatic data transfer into the personalized and secured online portal

Device: Step counter
self-monitoring of physical activity; with automatic data transfer into the personalized and secured online portal

Other: Access to the online portal
self-monitoring of health parameters

Experimental: TeLIPro group

The TeLIPro group will be provided a scale, a step counter, a blood glucose meter with test stripes as well as access to the online portal and will get telemedical coaching.

Device: Scale
self-monitoring of body weight; with automatic data transfer into the personalized and secured online portal

Device: Step counter
self-monitoring of physical activity; with automatic data transfer into the personalized and secured online portal

Device: Blood glucose meter with test stripes
self-monitoring of blood glucose; with automatic data transfer into the personalized and secured online portal

Other: Access to the online portal
self-monitoring of health parameters

Other: Telemedical coaching
regular telephone calls providing information about T2DM, healthy lifestyle, low-carbohydrate diet and physical activity

Outcome Measures

Primary Outcome Measures

  1. HbA1c change [12 months]

    estimated treatment difference between groups of HbA1c change (in T2DM patients with diabetes duration of ≥ 5 years)

  2. remission rate [12 months]

    number of participants with an HBA1c <6.5% (in T2DM patients with diabetes duration of < 5 years)

Secondary Outcome Measures

  1. fasting blood glucose change [12 months]

    estimated treatment difference between groups of fasting blood glucose change

  2. weight change [12 months]

    estimated treatment difference between groups of weight change

  3. body mass index change [12 months]

    estimated treatment difference between groups of body mass index change

  4. systolic blood pressure change [12 months]

    estimated treatment difference between groups of systolic blood pressure change

  5. diastolic blood pressure change [12 months]

    estimated treatment difference between groups of diastolic blood pressure change

  6. total cholesterol change [12 months]

    estimated treatment difference between groups of total cholesterol change

  7. high-density lipoprotein (HDL) cholesterol change [12 months]

    estimated treatment difference between groups of high-density lipoprotein (HDL) cholesterol change

  8. low-density lipoprotein (LDL) cholesterol change [12 months]

    estimated treatment difference between groups of low-density lipoprotein (LDL) cholesterol change

  9. triglyceride change [12 months]

    estimated treatment difference between groups of triglyceride change

  10. number of steps [12 months]

    estimated treatment difference between groups of number of steps

  11. antidiabetic medication change [12 months]

    estimated treatment difference between groups of antidiabetic medication change

  12. diabetes-specific treatment costs [12 months]

    estimated treatment difference between groups of diabetes-specific treatment costs

  13. inpatient costs [12 months]

    estimated treatment difference between groups of inpatient costs

  14. outpatient costs [12 months]

    estimated treatment difference between groups of outpatient costs

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 79 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Type 2 diabetes mellitus

  • body mass index of et least 27 kg/m2

Exclusion Criteria:
  • acute infections

  • chronic diseases other than type 2 diabetes and hypertension (e.g., cancer, chronic obstructive pulmonary disease, asthma, dementia, chronic gut diseases, psychoses, liver cirrhosis, macronephropathy/nephropathy, kidney insufficiency with glomerular filtration rate <30 ml/min/1.73 m2)

  • acute chemotherapy or chronic cortisol treatment

  • smoking cessation for <3 months and/or planned smoking cessation during study

  • pregnancy or breast-feeding

Contacts and Locations

Locations

Site City State Country Postal Code
1 West German Centre of Diabetes and Health Düsseldorf Germany 40591

Sponsors and Collaborators

  • West German Center of Diabetes and Health
  • AOK Rhineland / Hamburg
  • German Institute for Telemedicine and Health Promotion
  • German Diabetes Center

Investigators

  • Study Chair: Bernd Altpeter, Deutsches Institut für Telemedizin und Gesundheitsförderung
  • Study Chair: Sibel Altin, AOK Rhineland / Hamburg
  • Study Chair: Andrea Icks, PhD, Deusches Diabetes Zentrum

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Stephan Martin, Director, West German Center of Diabetes and Health
ClinicalTrials.gov Identifier:
NCT03675919
Other Study ID Numbers:
  • TeLIPro
First Posted:
Sep 18, 2018
Last Update Posted:
Oct 12, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Stephan Martin, Director, West German Center of Diabetes and Health
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 12, 2021