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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01688778
Other study ID # H-2-2011-158
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2012
Est. completion date April 28, 2015

Study information

Verified date September 2018
Source Bispebjerg Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to investigate the effect of telemedicine among the group of type-2-diabetics who, despite rehabilitation, remain poorly regulated. To describe the patients with regards to vulnerability and social resources and to determine wich groups benefit the most from telemedicine.


Description:

Type-2-diabetes is a growing healthcare problem. Both because of the increasing amount of patients and because of the complications of diabetes.

Non-pharmacological treatment is considered fundamental in the treatment of patients with type-2-diabetes.

In the Community of Copenhagen, all patients diagnosed with diabetes receive rehabilitation. The rehabilitation consists of counseling with regards to nutrition, physical activity, smoking cessation and education about diabetes.

Some patients however, remain poorly regulated despite rehabilitation as well as pharmacological treatment.

A total number of 165 patients will be randomized to intervention group or standard care.


Recruitment information / eligibility

Status Completed
Enrollment 165
Est. completion date April 28, 2015
Est. primary completion date April 28, 2015
Accepts healthy volunteers No
Gender All
Age group 30 Years to 75 Years
Eligibility Inclusion Criteria:

- HbA1c > 7,5%

- BMI > 25

- Spoken danish

- Completed a rehabilitation program more than 6 months ago

Exclusion Criteria:

- HbA1c < 7,5%

- BMI < 25

- Need of interpreter

Study Design


Intervention

Behavioral:
Telemedicine
Monthly video consultations with a nurse as add-on to standard treatment. The nurse has access to bloodsugar- bloodpressure and weight measurements uploaded by the participants to a tablet computer directly from the devices. Patients on Insulin measure bloodsugar twice a day (fasting and before their evening meal). Patients not on Insulin measure bloodsugar once a week (fasting and before their evening meal). All participants measure bloodpressure and weight once a week. The intervention lasts 32 weeks.

Locations

Country Name City State
Denmark Endocrine Section, Dept. of Internal Medicine I, Bispebjerg Hospital Copenhagen Copenhagen NV

Sponsors (2)

Lead Sponsor Collaborator
Bispebjerg Hospital The Health and Care Committee, Copenhagen City Council

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Number of hospital admissions 32 weeks
Other Number of visits at the emergency 32 weeks
Other Number of visits at the outpatient department 32 weeks
Other Number of visits at GP 32-weeks
Primary Changes in HbA1c Baseline, 16 weeks, 32 weeks, 6 months after intervention
Secondary Fasting total cholesterol, LDL, HDL, triglycerides Baseline, 32 weeks
Secondary Beta-cell function test (HOMA) Baseline, 32 weeks
Secondary Weight Baseline, 32 weeks
Secondary Bloodpressure Baseline, 32 weeks
Secondary Physical activity Baseline, 32 weeks
Secondary Change in quality of life Baseline, 32 weeks
Secondary Waist circumference Baseline, 32 weeks
Secondary Hip circumference Baseline, 32 weeks
Secondary Body mass index Baseline, 32 weeks
Secondary Use of medication Baseline, 32 weeks
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