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临床试验/NCT00850629
NCT00850629已完成不适用

Hormonal Regulation of Body Weight Maintenance

Charite University, Berlin, Germany1 个研究点 分布在 1 个国家目标入组 286 人开始时间: 2010年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
286
试验地点
1
主要终点
BMI will be assessed during lifestyle intervention in (1) children and adolescents and (2) adults vs. placebo

研究概览

简要总结

The investigators here propose to perform a collaborative clinical research effort including a randomized controlled trial investigating the mechanisms of weight maintenance and their relation to a lifestyle intervention in children, adolescents and adults. The detailed investigation and analysis of the variability and dynamics of the endocrine circuits responding to a negative energy balance and weight loss will be accompanied and enhanced by specific clinical projects targeting peripheral and central-nervous aspects of hormonal counter-regulation after weight loss. Mechanisms of endocrine counter-regulation and potential therapeutic approaches will be studied.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
10 Years 至 90 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •BMI > 27 kg/m2 (adults)

排除标准

  • •weight loss of more than 5kg in the last 2 months
  • •pregnancy, breastfeeding
  • •patients with:
  • •severe heart failure
  • •impaired hepatic or renal function
  • •disturbed coagulation (biopsies will not be taken in those subjects)
  • •infection, malabsorption
  • •severe hypertension
  • •cancer within the last 5 years
  • •eating disorders or any other psychiatric condition that would interact with the trial intervention
  • •any other endocrine disorder
  • •changes of smoking habits or diets within the last 3 months prior to study inclusion

研究组 & 干预措施

placebo

Placebo Comparator

Placebo

干预措施: placebo (Behavioral)

lifestyle intervention

Experimental

After an initial weight loss, the weight regain will be measured during multimodal lifestyle intervention in children, adolescents and adults

干预措施: multimodal lifestyle intervention (Behavioral)

结局指标

主要结局

BMI will be assessed during lifestyle intervention in (1) children and adolescents and (2) adults vs. placebo

时间窗: 21 months

BMI (kg/m2) will be analyzed after intentional weight loss in two comparable parts of a randomized controlled trial including (1) children and adolescents and (2) adults. Therefore effects of a multimodal lifestyle intervention will be compared to placebo.

次要结局

  • Evaluation of leptin during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of catecholamines during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of glucagon-like peptide 1 (GLP1) during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of leptin during follow up(48 months)
  • Evaluation of glucose-dependent insulinotropic polypeptide (GIP) during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of thyroid hormones during follow up(48 months)
  • Evaluation of insulin during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of catecholamines during follow up(48 months)
  • Evaluation of cortisol during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of GLP1 during follow up(48 months)
  • Evaluation of cortisol during follow up(48 months)
  • Evaluation of IGF1 during follow up(48 months)
  • BMI course after a lifestyle intervention in (1) children and adolescents and (2) adults vs. placebo(month 24, month 36, month 48)
  • changes of fatty acids during the intervention(month -3, month 0, month 12, month 18, month 24, month 36, month 48)
  • Evaluation of GIP during follow up(48 months)
  • Evaluation of thyroid hormones during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of insulin during follow up(48 months)
  • Evaluation of natriuretic peptide during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Evaluation of natriuretic peptide during follow up(48 months)
  • Evaluation of respiratory coefficient during lifestyle intervention(month -3, month 0, month 12, month 18, month 24, month 36, month 48)
  • Prediction of body weight regain(month 18, month 48)
  • Evaluation of insulin-like growth factor 1 (IGF1) during lifestyle intervention(month -3, month 0, month 12, month 18)
  • Prediction of energy expenditure(month 18, month 48)
  • body composition(month -3, month 0, month 12, month 18, month 24, month 36, month 48)
  • Measurement of messenger ribonucleic acid (mRNA) changes in adipose and skeletal muscle before (T-3), after weight loss (T0) and after as well as after 12 months randomized lifestyle intervention (or placebo)(month -3, month 0, month 12)
  • Prediction of insulin sensitivity(month 18, month 48)
  • changes acylcarnitines(month 12, month 18, month 24, month 36, month 48)
  • Evaluation of blood pressure during lifestyle intervention(month -3, month 0, month 12, month 18, month 24, month 36, month 48)
  • Evaluation of free fatty acids (FFAs) during lifestyle intervention(month -3, month 0, month 12, month 18, month 24, month 36, month 48)
  • Measurement of insulin sensitivity(month -3, month 0, month 12)
  • Prediction of muscle mass(month 18, month 48)
  • Prediction of fat mass(month 18, month 48)
  • changes acylcarnitines(month -3, month 0)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Professor Joachim Spranger

Professor

Charite University, Berlin, Germany

研究点 (1)

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