Effect of Type 2 Diabetes Genetic Risk Information on Health Behaviors and Outcomes (TDE)
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| First Received Date ICMJE | February 22, 2009 | ||||||||||||||||||||||||||||
| Last Updated Date | March 18, 2013 | ||||||||||||||||||||||||||||
| Start Date ICMJE | April 2009 | ||||||||||||||||||||||||||||
| Primary Completion Date | September 2011 (final data collection date for primary outcome measure) | ||||||||||||||||||||||||||||
| Current Primary Outcome Measures ICMJE |
Percentage of weight loss [ Time Frame: 12 months ] [ Designated as safety issue: No ] | ||||||||||||||||||||||||||||
| Original Primary Outcome Measures ICMJE | Same as current | ||||||||||||||||||||||||||||
| Change History | Complete list of historical versions of study NCT00849563 on ClinicalTrials.gov Archive Site | ||||||||||||||||||||||||||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE | Same as current | ||||||||||||||||||||||||||||
| Current Other Outcome Measures ICMJE | Not Provided | ||||||||||||||||||||||||||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||||||||||||||||||||||||||
| Descriptive Information | |||||||||||||||||||||||||||||
| Brief Title ICMJE | Effect of Type 2 Diabetes Genetic Risk Information on Health Behaviors and Outcomes | ||||||||||||||||||||||||||||
| Official Title ICMJE | Effect of Type 2 Diabetes Genetic Risk Information on Health Behaviors and Outcomes | ||||||||||||||||||||||||||||
| Brief Summary | The primary objective of the study is to assess the clinical utility of a genetic test for Type 2 diabetes risk in combination with standardized risk assessment compared with standardized risk assessment alone, and to measure whether changes in perceived risk following genetic testing for Type 2 diabetes risk are correlated with behavior change and increased concern about risk for Type 2 diabetes. |
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| Detailed Description | One thousand outpatients will be enrolled over two years at two university-affiliated primary care clinics. Patients will be assigned to one of three study arms: those who want genetic testing for diabetes risk will be randomly assigned to either receive the testing in addition to the SRA (SRA+G) or to receive the SRA only (SRA-only). Those who do not wish to have genetic testing will receive the SRA only. All patients will be surveyed at baseline, immediately after going through the SRA (risk-counseling visit; 2-4 weeks after initial visit), at 3 months post risk counseling visit and at 12 months post risk counseling visit. BMI, waist circumference, fasting plasma glucose and insulin will be measured at baseline and 12 months. Surveys will allow us to track patients' emotional responses to diabetes risk information and changing perceptions of personal risk for Type 2 diabetes over time, and to see if these correlate with subsequent diet and exercise behaviors. We will use a linear model to assess the effects of genetic testing among the three study groups, using HOmeostasis Model Assessment of Insulin Resistance (HOMA-IR) and weight loss as the primary outcomes. We will use generalized linear ordinal regression models to fit the ordinal survey outcomes of risk perceptions to the continuous HOMA-IR and weight outcome variables. |
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| Study Type ICMJE | Interventional | ||||||||||||||||||||||||||||
| Study Phase | Not Provided | ||||||||||||||||||||||||||||
| Study Design ICMJE | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Prevention |
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| Condition ICMJE | Diabetes Mellitus, Type 2 | ||||||||||||||||||||||||||||
| Intervention ICMJE | Other: Standardized Risk Assessment
patients interested in genetic testing will be randomly assigned to either get testing for type 2 diabetes or not. All arms with receive standardized risk asessements. This study is evaluating behavior after receipt of genetic risk information and different types of counseling. |
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| Study Arm (s) |
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| Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |||||||||||||||||||||||||||||
| Recruitment Status ICMJE | Active, not recruiting | ||||||||||||||||||||||||||||
| Estimated Enrollment ICMJE | 1000 | ||||||||||||||||||||||||||||
| Estimated Completion Date | June 2013 | ||||||||||||||||||||||||||||
| Primary Completion Date | September 2011 (final data collection date for primary outcome measure) | ||||||||||||||||||||||||||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||||||||||||||||||||||||||
| Ages | 18 Years to 80 Years | ||||||||||||||||||||||||||||
| Accepts Healthy Volunteers | Yes | ||||||||||||||||||||||||||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||||||||||||||||||||||||||
| Location Countries ICMJE | United States | ||||||||||||||||||||||||||||
| Administrative Information | |||||||||||||||||||||||||||||
| NCT Number ICMJE | NCT00849563 | ||||||||||||||||||||||||||||
| Other Study ID Numbers ICMJE | Pro00011592 | ||||||||||||||||||||||||||||
| Has Data Monitoring Committee | No | ||||||||||||||||||||||||||||
| Responsible Party | Duke University | ||||||||||||||||||||||||||||
| Study Sponsor ICMJE | Duke University | ||||||||||||||||||||||||||||
| Collaborators ICMJE | deCODE genetics | ||||||||||||||||||||||||||||
| Investigators ICMJE |
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| Information Provided By | Duke University | ||||||||||||||||||||||||||||
| Verification Date | December 2012 | ||||||||||||||||||||||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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