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Clinical Trials/NCT01339208
NCT01339208
Completed
N/A

TREAT (Telemedicine for Reach, Education, Access, and Treatment)

University of Pittsburgh1 site in 1 country35 target enrollmentJune 2011
ConditionsType 2 Diabetes

Overview

Phase
N/A
Intervention
Not specified
Conditions
Type 2 Diabetes
Sponsor
University of Pittsburgh
Enrollment
35
Locations
1
Primary Endpoint
Change in HbA1c % from baseline
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the feasibility and clinical efficacy of an innovative care model that combines Telemedicine consultations, educator therapeutic management and diabetes education to empower patients to be in greater control of their own diabetes care for improvements in diabetes outcomes.

Detailed Description

This study will assess whether a new care delivery model combining telemedicine videoconference diabetes consultations with diabetes self-management teaching is efficacious in reducing HbA1c in patients with type 2 diabetes in rural areas. The control group will consist of patients with type 2 diabetes receiving "usual care", i.e., who have not received a referral to the endocrinologist telemedicine team. Secondary outcomes include patient satisfaction, level of understanding of self-management skills, and hypoglycemia

Registry
clinicaltrials.gov
Start Date
June 2011
End Date
March 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Linda Siminerio

Director Diabetes Institute

University of Pittsburgh

Eligibility Criteria

Inclusion Criteria

  • Age 18 or older with type 2 diabetes
  • Referral by a primary care provider.
  • HbA1c equal or greater than 7.0%.

Exclusion Criteria

  • Type 1 diabetes
  • Gestational Diabetes

Outcomes

Primary Outcomes

Change in HbA1c % from baseline

Time Frame: 3 and 6 month

Secondary Outcomes

  • Patient satisfaction(6 month)

Study Sites (1)

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