Status:

COMPLETED

Situational Problem Solving in Adolescents With Type 2 Diabetes: Enhancing a Randomized Controlled Trial (RCT)

Lead Sponsor:

Vanderbilt University

Collaborating Sponsors:

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Conditions:

Adolescents With Type 2 Diabetes

Eligibility:

All Genders

12-19 years

Phase:

NA

Brief Summary

The proposed research will test a new comprehensive disease management intervention with adolescents who have type 2 diabetes using a randomized controlled trial (RCT). Adolescents subjects with a his...

Eligibility Criteria

Inclusion

  • Patients with a diagnosis of T2DM will be included if they are:
  • Age 12-19 years
  • A clinical diagnosis of T2DM (according to the patient and their health provider in the clinic)
  • Actively receive diabetes care in the Eskind Diabetes Clinic
  • Willingness of patient and a caregiver to access the Internet to complete problem solving activities
  • Adolescent address is the same as their primary caregiver participating in the study

Exclusion

  • Patients will be excluded if they meet any of the following:
  • Identify an outside practitioner as the main provider of their diabetes care
  • Have a significant psychiatric illness such as severe depression or active psychosis that would impact on the ability to participate in the study
  • Life expectancy of \<6 months
  • Unable to access the Internet from any convenient location
  • Blind or deaf
  • Parent Inclusion criteria:
  • Parents must be a primary caregiver of an adolescent with a diagnosis of T2DM between the ages 12-19 seen at the Eskind Clinic
  • Willingness of patient and a caregiver to access the Internet to complete problem solving activities.
  • Parent Exclusion criteria:
  • Patients will be excluded if they meet any of the following:
  • Identify an outside practitioner as the main provider of their child's diabetes care
  • Self report of significant psychiatric illness such as severe depression or active psychosis that would impact on the ability to participate in the study
  • life expectancy of \<6 months
  • unable to access the Internet from any convenient location
  • blind or deaf.
  • Joint Inclusion criteria:
  • Both the primary caregiver (parent) and adolescent must agree to participate in the research.

Key Trial Info

Start Date :

June 1 2009

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

August 1 2011

Estimated Enrollment :

43 Patients enrolled

Trial Details

Trial ID

NCT00889785

Start Date

June 1 2009

End Date

August 1 2011

Last Update

December 18 2013

Active Locations (1)

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1

Vanderbilt Univ Medical Center

Nashville, Tennessee, United States, 37232