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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04595383
Other study ID # 2020/09
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 1, 2021
Est. completion date May 31, 2022

Study information

Verified date March 2021
Source Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the efficacy of an electronic platform for doctor-patient communication in order to reduce severe and non-severe hypoglycemia events as well as inadvertent hypoglycemia events.


Description:

This is an open randomized clinical trial without drugs. Patients with type 2 diabetes and treated with insulin will be included. Patients allocated in the intervention group will use the electronic platform as a communication channel with their health provider during the time between visits. The name of the platform is ti.care (https://ti.care/es) and it will be a complement of the control visits to resolve doubts through chats, email or video call. Health providers will answer the patient requests.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 106
Est. completion date May 31, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Aged over 17 years - Patients with type 2 diabetes diagnosis - Patients who start insulin treatment or with intensification of treatment - Patients who sign informed consent Exclusion Criteria: - Patients with type 1 diabetes diagnosis - Life expectancy less than one year - Pregnancy - Patients with dementia - Patients with treatment different to insulin - Patients who, in the opinion of the researcher, cannot follow the recommendations of the self-care health education plan.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
ti.care
Electronic platform for doctor-patient communication

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana

Outcome

Type Measure Description Time frame Safety issue
Primary Change from HbA1c level at 3 months Change from HbA1c level at 3 months Baseline and at 3 months
Primary Change from basal capillary blood glucose at 3 months Change from basal capillary blood glucose at 3 months Baseline and at 3 months
Primary Change from postprandial blood glucose at 3 months Change from postprandial blood glucose at 3 months Baseline and at 3 months
Primary Change from nocturnal blood glucose at 3 months Change from nocturnal blood glucose at 3 months Baseline and at 3 months
Primary Total hypoglycemia Number of total hypoglycemia events At 3 months
Primary Number of nocturnal hypoglycemia events Number of nocturnal hypoglycemia events At 3 months
Primary Number of inadvertent hypoglycemia events Number of inadvertent hypoglycemia events At 3 months
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