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Type 1 Diabetes Mellitus clinical trials

View clinical trials related to Type 1 Diabetes Mellitus.

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NCT ID: NCT03506711 Completed - Clinical trials for Coronary Artery Disease

Isometric Handgrip Exercise -MRI in Children and Adolescents

Start date: February 1, 2016
Phase: N/A
Study type: Interventional

This project aims to assess coronary vessel response to isometric handgrip exercise (IHE) during magnetic resonance imaging (MRI) in children with T1D children and healthy controls. The investigators will compare the groups in terms of surrogate markers of intima media alteration and arterial stiffness, i.e. carotid intima media thickness (CIMT) and aortic pulse wave velocity (PWV).

NCT ID: NCT03505268 Recruiting - Clinical trials for Type 1 Diabetes Mellitus

The Impact of Telehealthcare Intervention on Glycemic Control in Children and Adolescents With Type 1 Diabetes

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

This study evaluates the effect of telemedicine intervention program upon glycemic control in type 1 diabetes mellitus children and their parents in Israel. Half of the participants will receive the telemedicine intervention for a period of six months while the other half will receive the regular treatment then vice versa. Each group will receive in the intervention period 6 telemedicine meeting with a dietician and six telemedicine meetings with a nurse. The investigators hypothesized that the participants that are recieving the telemedicine intervention will have a better glycemic control after 6 months.

NCT ID: NCT03504046 Completed - Clinical trials for Type 1 Diabetes Mellitus

Safety and Feasibility Evaluation of the APS APP

Start date: February 28, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

This clinical trial is a safety and feasibility study to assess the performance of artificial pancreas (AP) system using the Zone Model Predictive control (Zone-MPC) and Health Monitoring System (HMS) algorithms embedded into the APS APP platform.

NCT ID: NCT03497260 Completed - Clinical trials for Type 1 Diabetes Mellitus

Fructose in Exercising Individuals With Type 1 Diabetes Using Insulin Degludec

FruDeg
Start date: January 4, 2019
Phase: N/A
Study type: Interventional

To determine and compare the time-to-hypoglycaemia (defined as plasma glucose <3.9mmol/L) in individuals with type 1 diabetes treated with ultra-Long acting insulin degludec during aerobic exercise with or without prior ingestion of a single oral fructose load.

NCT ID: NCT03490773 Completed - Clinical trials for Type 1 Diabetes Mellitus

Type 1 Diabetes, Immunology, Genetics & Endogenous Insulin Production

TIGI
Start date: November 1, 2014
Phase:
Study type: Observational

Type I diabetes(T1D)T occurs when an individual loses the ability to make enough insulin to control their blood sugar levels. They need insulin injections to replace the insulin production that has been lost. Traditionally people with T1D are thought to make none of their own insulin after diagnosis, but we have recently identified that there are some people who have T1D but go one making insulin for many years. We would like to explore this in more depth and understand why some people with T1D go on making insulin and some do not. This will help us understand the causes of T1D and may help work out ways to protect this remaining insulin production, with improved blood sugar control, and reduced long-term complications of diabetes We aim to explore genetic and immunological factors which impact on the ability of an individual diagnosed with Type I diabetes (T1D) to produce their own insulin. We aim to study individuals who have been diagnosed with T1D with variable duration and assess the genetic and immunological profile of those whose are thought to be producing significant amounts of insulin despite a long duration and those who despite a very short duration, lose insulin production very quickly.

NCT ID: NCT03484741 Recruiting - Clinical trials for Type 1 Diabetes Mellitus

Mesenchymal Stem Cell Therapy for Type 1 Diabetes Mellitus Patients

Start date: April 1, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of mesenchymal stem cells (MSCs) transplantation for type 1 Diabetes Mellitus patients.

NCT ID: NCT03478254 Completed - Clinical trials for Type 1 Diabetes Mellitus

Adherence to Guidelines VAccination in Type 1 DIabetes Mellitus Patients (AVADI-1).

AVADI-1
Start date: December 1, 2017
Phase:
Study type: Observational

Observational study about adherence to guidelines for Influenza, Pneumococcal and Hepatitis B Vaccination in adult patients with type 1 Diabetes mellitus.

NCT ID: NCT03475108 Active, not recruiting - Diabetes Mellitus Clinical Trials

Integrating Community Health Workers Into the Care of Children With Type 1 Diabetes

Start date: April 19, 2018
Phase: N/A
Study type: Interventional

The primary aim of this randomized controlled trial is to determine if the integration of a Community Health Worker into the healthcare team is associated with an improvement in diabetes control in children with type 1 diabetes. The secondary objectives are to determine if utilization of Community Health Workers is also associated with reduced emergency department visits and hospitalizations, improved attendance at outpatient diabetes appointments, and improvements in psychosocial outcomes and diabetes control.

NCT ID: NCT03473704 Recruiting - Depression Clinical Trials

Telematic Program for the Treatment of Depression in Type 1 Diabetes

Start date: January 19, 2017
Phase: N/A
Study type: Interventional

In diabetes, web programs have been designed that have integrated cognitive-behavioral therapy (CBT) with diabetes education, obtaining positive results in the mood of the patient. In Spain, no similar approach has been performed in people with diabetes and depression. However, the need to provide professionals with adequate tools to help people with this problem is justified. The main objective of this project is to apply a telematic program for the treatment of specific depression for people with type 1 diabetes designed by our research team in a sample of patients with type 1 diabetes and mild-moderate depressive symptomatology of the province of Malaga. To do this, the sample will be divided into two groups: treatment group (TG) and control group (CG). The design of the study is quasi-experimental, longitudinal randomized pre-post with control group. The treatment group (TG) will receive the web treatment, which consists of 9 weekly sessions, while the control group (CG) will be evaluated in the same phases as the TG. For ethical reasons, the CG will receive the web treatment once the TG intervention has been completed. There will be a follow-up at 3, 6 and 12 months.

NCT ID: NCT03466398 Withdrawn - Diabetes Mellitus Clinical Trials

Effects of a Remote Patient Monitoring Protocol on Glycemic Control in Adolescents With Type 1 Diabetes

Start date: April 11, 2018
Phase: N/A
Study type: Interventional

This study will use a randomized, crossover design. Children aged 13-18 years who have been diagnosed with Type 1 diabetes for at least 1 year and with at least 2 Hemoglobin A1c values ≥10.0% more than 60 days apart within the past year, with the most recent HbA1c value between 10-14%, will be placed into two separate treatment groups. Group A will undergo home monitoring for 12 weeks through the use of the Vivify kit, which contains a wireless tablet with daily medication/diet/symptom questionnaires. Group B will initially continue diabetes management per standard of care, including quarterly office visits. After a period of 12 weeks, Group B will switch to the RPM protocol, while Group A will return to standard of care. Both groups will have HbA1c values checked at the 0, 3, and 6 month time periods to assess the effect of the remote monitoring protocol. Participation in the RPM protocol will involve daily completion of the Care Plan questions, as well as weekly uploads of blood glucose values using the Glooko, Inc (Mountain View, CA) application, and weekly video visits with a member of the endocrinology team that will aim to address barriers to optimal care, whether they be motivation, knowledge or other difficulties. Barriers to care will be assessed in part through the completion of knowledge and self-efficacy assessments.