Evaluation of a Treatment and Education Programme for Type 1 Diabetic Patients (PRIMAS)
| Tracking Information | |||||
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| First Received Date ICMJE | October 12, 2010 | ||||
| Last Updated Date | May 31, 2012 | ||||
| Start Date ICMJE | September 2010 | ||||
| Primary Completion Date | March 2012 (final data collection date for primary outcome measure) | ||||
| Current Primary Outcome Measures ICMJE |
Improvement of glycemic control measured by A1c [ Time Frame: 6 month ] [ Designated as safety issue: No ] Difference between baseline A1c and A1c at 6 month follow up |
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| Original Primary Outcome Measures ICMJE |
A1c [ Time Frame: 6 month after termination of educational interventions ] [ Designated as safety issue: No ] | ||||
| Change History | Complete list of historical versions of study NCT01220557 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE |
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| Current Other Outcome Measures ICMJE | Not Provided | ||||
| Original Other Outcome Measures ICMJE | Not Provided | ||||
| Descriptive Information | |||||
| Brief Title ICMJE | Evaluation of a Treatment and Education Programme for Type 1 Diabetic Patients (PRIMAS) | ||||
| Official Title ICMJE | Prospective Randomized Trial for the Evaluation of a Treatment and Education Programme for Type 1 Diabetic Patients (PRIMAS) | ||||
| Brief Summary | This study is a randomized prospective trial with 6-month follow up. A non-inferiority hypothesis is tested. A new developed treatment and education programme for type 1 diabetic will be tested compared to an established treatment and education programme. Primary outcome variable is glycemic control in a 6-month follow up. Secondary outcome variables are: diabetes knowledge, diabetes related distress, depressive symptoms, self care behavior, metabolic risk factors, quality of life, attitudes towards diabetes and insulin treatment. |
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| Detailed Description | Both programmes consists of 12 lessons with a length of 90 minutes. Eligible type 1 diabetic patients in a diabetologist practice are pooled and randomised either to the new developed PRIMAS programme or to an established education programme for type 1 diabetic patients (Treatment and education programme for intensified insulin treatment) as an active comparator. Inclusion criteria: type 1 diabetes diabetes duration > 4 weeks age 18 - 75 years BMI 20 - 40 kg/m² A1c > 6.9% and < 13.1% no structured diabetes education during the last 12 months wish to participate in a group education fluent in reading and speaking German language informed consent Exclusion criteria: severe organic disease (e.g. terminal renal disease, cancer with poor prognosis) current treatment of a mental disease Cognitive impairment - dementia pregnancy |
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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: Open Label Primary Purpose: Treatment |
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| Condition ICMJE | Type 1 Diabetes | ||||
| Intervention ICMJE |
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| Study Arm (s) |
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| Publications * | Not Provided | ||||
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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 | Completed | ||||
| Enrollment ICMJE | 162 | ||||
| Completion Date | March 2012 | ||||
| Primary Completion Date | March 2012 (final data collection date for primary outcome measure) | ||||
| Eligibility Criteria ICMJE | Inclusion Criteria: type 1 diabetes diabetes duration > 4 weeks age 18 - 75 years BMI 20 - 40 kg/m² A1c > 6.9% and < 13.1% no structured diabetes education during the last 12 months wish to participate in a group education fluent in reading and speaking German language informed consent Exclusion Criteria: severe organic disease (e.g. terminal renal disease, cancer with poor prognosis) current treatment of a mental disease Cognitive impairment - dementia pregnancy |
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| Gender | Both | ||||
| Ages | 18 Years to 75 Years | ||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | Germany | ||||
| Administrative Information | |||||
| NCT Number ICMJE | NCT01220557 | ||||
| Other Study ID Numbers ICMJE | NH062010 | ||||
| Has Data Monitoring Committee | No | ||||
| Responsible Party | Norbert Hermanns, Forschungsinstitut der Diabetes Akademie Mergentheim | ||||
| Study Sponsor ICMJE | Forschungsinstitut der Diabetes Akademie Mergentheim | ||||
| Collaborators ICMJE | Not Provided | ||||
| Investigators ICMJE |
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| Information Provided By | Forschungsinstitut der Diabetes Akademie Mergentheim | ||||
| Verification Date | May 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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