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Telemedicine Influence in the Follow up of the Type 2 Diabetes Patient

P

Province of Malaga Health Department

Status

Completed

Conditions

Self Monitoring Blood Glucose
Type 2 Diabetes
Primary Care
Telemedicine

Treatments

Device: Telemedicine system

Study type

Interventional

Funder types

Other

Identifiers

NCT00527254
TeleDiabecom 200501

Details and patient eligibility

About

The purpose of this study is to evaluate the impact of a a real time teleassistance system in the clinical evolution of type 2 diabetic patients on self monitoring blood glucose in the Public National Primary Care System.

Full description

The UKPDS study in type 2 diabetes and the DCCT in type 1, showed that intensive blood glucose control and the following HBA1c decrease were associated with a decrease of diabetic complications. Introducing telecontrol elements in the real time follow up of the patients, should help to know continuously patient blood glucose profile and add if necessary immediately therapeutical variations, to maintain HbA1c levels as low as possible.

The study compares type 2 diabetes patients performing self monitoring of blood glucose, followed up by their family doctor in their primary care unit with the extra support of a real time teleassistance system with type 2 diabetes patients performing self monitoring of blood glucose, followed up by their family doctor in their primary care unit.

Enrollment

328 patients

Sex

All

Ages

30+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of type 2 Diabetes
  • on SMBG al least 6 months before
  • age superior of 30 years
  • controlled in province of Málaga Primary Care Units

Exclusion criteria

  • having diabetic complications or other diseases that could make difficult to use the telemedicine system
  • patients who need a carer
  • not passing the initial training (low cultural level)
  • living in an area without mobile phone coverage

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

328 participants in 2 patient groups

Control group
No Intervention group
Telemedicine group
Active Comparator group
Treatment:
Device: Telemedicine system

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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