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