Efficacy of the Telemedical Lifestyle intervention Program TeLiPro in Advanced Stages of Type 2 Diabetes: A Randomized Controlled Trial

被引:130
作者
Kempf, Kerstin [1 ]
Altpeter, Bernd [2 ]
Berger, Janine [2 ]
Reuss, Oliver [3 ]
Fuchs, Matthias [3 ]
Schneider, Michael [4 ,5 ]
Gaertner, Babette [1 ]
Niedermeier, Katja [1 ]
Martin, Stephan [1 ,6 ]
机构
[1] Dusseldorf Catholic Hosp Grp, West German Ctr Diabet & Hlth, Dusseldorf, Germany
[2] German Inst Telemed & Healthpromot, Dusseldorf, Germany
[3] Boehringer Ingelheim GmbH & Co KG, Ingelheim, Germany
[4] Boehringer Ingelheim Pharma GmbH & Co KG, Ingelheim, Germany
[5] Heidelberg Univ, Med Fac Mannheim, Mannheim Inst Publ Hlth, Mannheim, Germany
[6] Heinrich Heine Univ Dusseldorf, Fac Med, Dusseldorf, Germany
关键词
CONTROLLED-RELEASE PHENTERMINE/TOPIRAMATE; CLINICAL ENDOCRINOLOGISTS; CARDIOVASCULAR-DISEASE; AMERICAN ASSOCIATION; UNITED-STATES; WEIGHT-LOSS; POSITION STATEMENT; METABOLIC SYNDROME; BARIATRIC SURGERY; PHYSICAL-ACTIVITY;
D O I
10.2337/dc17-0303
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Lifestyle interventions are the foundation of treatment in newly diagnosed type 2 diabetes. However, their therapeutic potential in advanced disease stages is unknown. We evaluated the efficacy of the Telemedical Lifestyle intervention Program (TeLiPro) in improving metabolic control in advanced-stage type 2 diabetes. RESEARCH DESIGN AND METHODS In this single-blind, active comparator, intervention study, patients with type 2 diabetes (with glycated hemoglobin [HbA(1c)] >= 7.5% [58.5 mmol/mol]), and BMI >= 27 kg/m(2) and on >= 2 antidiabetes medications) were recruited in Germany and randomized 1:1 using an electronically generated random list and sealed envelopes into two parallel groups. The data analyst was blinded after assignment. The control group (n = 100) got weighing scales and step counters and remained in routine care. The TeLiPro group (n = 102) additionally received telemedical coaching including medical-mental motivation, a formula diet, and self-monitored blood glucose for 12 weeks. The primary end point was the estimated treatment difference in HbA1c reduction after 12 weeks. All available values per patient (n = 202) were analyzed. Analyses were also performed at 26 and 52 weeks of follow-up. RESULTS HbA(1c) reduction was significantly higher in the TeLiPro group (mean 6 SD -1.1 +/- 1.2% vs. 20.2 6 0.8%; P < 0.0001). The estimated treatment difference in the fully adjusted model was 0.8% (95% CI 1.1; 0.5) (P < 0.0001). Treatment superiority of TeLiPro was maintained during follow-up (week 26: 0.6% [95% CI 1.0; 0.3], P = 0.0001; week 52: 0.6% [0.9; 0.2], P < 0.001). The same applies for secondary outcomes: weight (TeLiPro -6.2 +/- 4.6 kg vs. control -1.0 +/- 3.4 kg), BMI (-2.1 +/- 1.5 kg/m(2) vs. -0.3 +/- 1.1 kg/m(2)), systolic blood pressure (-5.7 +/- 15.3 mmHg vs. -1.6 +/- 13.8 mmHg), 10-year cardiovascular disease risk, antidiabetes medication, and quality of life and eating behavior (P < 0.01 for all). The effects were maintained long-term. No adverse events were reported. CONCLUSIONS In advanced-stage type 2 diabetes, TeLiPro can improve glycemic control and may offer new options to avoid pharmacological intensification.
引用
收藏
页码:863 / 871
页数:9
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