- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT00850629
Hormonal Regulation of Body Weight Maintenance
12 января 2018 г. обновлено: Professor Joachim Spranger, Charite University, Berlin, Germany
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.
Обзор исследования
Статус
Завершенный
Условия
Вмешательство/лечение
Тип исследования
Интервенционный
Регистрация (Действительный)
286
Фаза
- Непригодный
Контакты и местонахождение
В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.
Места учебы
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Berlin, Германия, 12200
- Charité
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Критерии участия
Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.
Критерии приемлемости
Возраст, подходящий для обучения
От 10 лет до 90 лет (Ребенок, Взрослый, Пожилой взрослый)
Принимает здоровых добровольцев
Да
Полы, имеющие право на обучение
Все
Описание
Inclusion Criteria:
- BMI > 27 kg/m2 (adults)
Exclusion Criteria:
- weight loss of more than 5kg in the last 2 months
- pregnancy, breastfeeding
patients with:
- severe heart failure
- impaired hepatic or renal function
- anaemia
- 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
Учебный план
В этом разделе представлена подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
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Плацебо Компаратор: плацебо
Плацебо
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никакого вмешательства, только сопровождение
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Экспериментальный: lifestyle intervention
After an initial weight loss, the weight regain will be measured during multimodal lifestyle intervention in children, adolescents and adults
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After an initial weight loss, the weight regain will be measured during multimodal lifestyle intervention in children, adolescents and adults
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Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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BMI will be assessed during lifestyle intervention in (1) children and adolescents and (2) adults vs. placebo
Временное ограничение: 21 months
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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.
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21 months
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Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Evaluation of leptin during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of leptin at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of leptin during follow up
Временное ограничение: 48 months
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Measurement of leptin during follow up until the 48 months
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48 months
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Evaluation of catecholamines during follow up
Временное ограничение: 48 months
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Measurement of catecholamines during follow up until the 48 months
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48 months
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Evaluation of catecholamines during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of catecholamines at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of cortisol during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of cortisol at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of cortisol during follow up
Временное ограничение: 48 months
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Measurement of cortisol during follow up until the 48 months
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48 months
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Evaluation of glucagon-like peptide 1 (GLP1) during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of GLP1 at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of GLP1 during follow up
Временное ограничение: 48 months
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Measurement of GLP1 during follow up until the 48 months
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48 months
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Evaluation of glucose-dependent insulinotropic polypeptide (GIP) during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of GIP at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of GIP during follow up
Временное ограничение: 48 months
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Measurement of GIP during follow up until the 48 months
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48 months
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Evaluation of thyroid hormones during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of thyroid hormones at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of thyroid hormones during follow up
Временное ограничение: 48 months
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Measurement of thyroid hormones during follow up until the 48 months
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48 months
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Evaluation of insulin during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of insulin at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of insulin during follow up
Временное ограничение: 48 months
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Measurement of insulin during follow up until the 48 months
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48 months
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Evaluation of insulin-like growth factor 1 (IGF1) during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of IGF1 at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of IGF1 during follow up
Временное ограничение: 48 months
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Measurement of IGF1 during follow up until the 48 months
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48 months
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Evaluation of natriuretic peptide during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18
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Measurement of natriuretic peptide at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and after additional 6 months follow up
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month -3, month 0, month 12, month 18
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Evaluation of natriuretic peptide during follow up
Временное ограничение: 48 months
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Measurement of natriuretic peptide during follow up until the 48 months
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48 months
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Evaluation of blood pressure during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Measurement of blood pressure at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and and after additional 36 months follow up
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month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Evaluation of free fatty acids (FFAs) during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Measurement of FFAs at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and and after additional 36 months follow up
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month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Evaluation of respiratory coefficient during lifestyle intervention
Временное ограничение: month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Measurement of respiratory coefficient at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and and after additional 36 months follow up
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month -3, month 0, month 12, month 18, month 24, month 36, month 48
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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)
Временное ограничение: month -3, month 0, month 12
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Measurement of systemic and tissue specific changes in adipose tissue and skeletal muscle using RNA sequencing (counts)
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month -3, month 0, month 12
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Measurement of insulin sensitivity
Временное ограничение: month -3, month 0, month 12
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Measurement of systemic and tissue specific changes in adipose and muscle insulin sensitivity using hyperinsulinemic clamp (mg•kg-1•min-1/(mU•L-1)) before (T-3), after weight loss (T0) and after as well as after 12 months randomized lifestyle intervention (or placebo)
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month -3, month 0, month 12
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Prediction of body weight regain
Временное ограничение: month 18, month 48
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No additional measurement will be done.
However, we will analyse the predictive impact of already measured parameters on long-term course of BMI (18 and 48 months) using mathematical models
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month 18, month 48
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Prediction of insulin sensitivity
Временное ограничение: month 18, month 48
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No additional measurement will be done.
However, we will analyse the predictive impact of already measured parameters on insulin sensitivity (18 and 48 months) using mathematical models
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month 18, month 48
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Prediction of energy expenditure
Временное ограничение: month 18, month 48
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No additional measurement will be done.
However, we will analyse the predictive impact of already measured parameters on energy expenditure (18 and 48 months) using mathematical models
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month 18, month 48
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Prediction of muscle mass
Временное ограничение: month 18, month 48
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No additional measurement will be done.
However, we will analyse the predictive impact of already measured parameters on muscle mass (18 and 48 months) using mathematical models
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month 18, month 48
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Prediction of fat mass
Временное ограничение: month 18, month 48
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No additional measurement will be done.
However, we will analyse the predictive impact of already measured parameters on fat mass (18 and 48 months) using mathematical models
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month 18, month 48
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BMI course after a lifestyle intervention in (1) children and adolescents and (2) adults vs. placebo
Временное ограничение: month 24, month 36, month 48
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BMI (kg/m2) after the randomized control trial (RCT) (18 months) will be analyzed up to 48 months.
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month 24, month 36, month 48
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changes of fatty acids during the intervention
Временное ограничение: month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Analysis of fatty acids at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and and after additional 36 months follow up
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month -3, month 0, month 12, month 18, month 24, month 36, month 48
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changes acylcarnitines
Временное ограничение: month -3, month 0
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Analysis of acylcarnitines at baseline and after 3 months of weight loss
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month -3, month 0
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changes acylcarnitines
Временное ограничение: month 12, month 18, month 24, month 36, month 48
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Analysis of acylcarnitines after 12 months randomized lifestyle intervention (or placebo) and and after additional 36 months follow up
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month 12, month 18, month 24, month 36, month 48
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body composition
Временное ограничение: month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Whole body fat mass (kg, %) will be measured at baseline, after 3 months of weight loss, as well as after 12 months randomized lifestyle intervention (or placebo) and and after additional 36 months follow up
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month -3, month 0, month 12, month 18, month 24, month 36, month 48
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Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Соавторы
Публикации и полезные ссылки
Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.
Общие публикации
- Li L, Soll D, Leupelt V, Spranger J, Mai K. Weight loss-induced improvement of body weight and insulin sensitivity is not amplified by a subsequent 12-month weight maintenance intervention but is predicted by adaption of adipose atrial natriuretic peptide system: 48-month results of a randomized controlled trial. BMC Med. 2022 Jul 28;20(1):238. doi: 10.1186/s12916-022-02435-9.
- Soll D, Gawron J, Pletsch-Borba L, Spranger J, Mai K. Long-term impact of the metabolic status on weight loss-induced health benefits. Nutr Metab (Lond). 2022 Mar 28;19(1):25. doi: 10.1186/s12986-022-00660-w.
- Li L, Spranger L, Stobaus N, Beer F, Decker AM, Wernicke C, Brachs S, Brachs M, Spranger J, Mai K. Fetuin-B, a potential link of liver-adipose tissue cross talk during diet-induced weight loss-weight maintenance. Nutr Diabetes. 2021 Oct 5;11(1):31. doi: 10.1038/s41387-021-00174-z.
- Li L, Spranger L, Soll D, Beer F, Brachs M, Spranger J, Mai K. Metabolic impact of weight loss induced reduction of adipose ACE-2 - Potential implication in COVID-19 infections? Metabolism. 2020 Dec;113:154401. doi: 10.1016/j.metabol.2020.154401. Epub 2020 Oct 13.
- Brachs S, Polack J, Brachs M, Jahn-Hofmann K, Elvert R, Pfenninger A, Barenz F, Margerie D, Mai K, Spranger J, Kannt A. Genetic Nicotinamide N-Methyltransferase (Nnmt) Deficiency in Male Mice Improves Insulin Sensitivity in Diet-Induced Obesity but Does Not Affect Glucose Tolerance. Diabetes. 2019 Mar;68(3):527-542. doi: 10.2337/db18-0780. Epub 2018 Dec 14.
- Mai K, Li L, Wiegand S, Brachs M, Leupelt V, Ernert A, Kuhnen P, Hubner N, Robinson P, Chen W, Krude H, Spranger J. An Integrated Understanding of the Molecular Mechanisms of How Adipose Tissue Metabolism Affects Long-term Body Weight Maintenance. Diabetes. 2019 Jan;68(1):57-65. doi: 10.2337/db18-0440. Epub 2018 Nov 2.
- Bau AM, Ernert A, Krude H, Wiegand S. Hormonal regulatory mechanisms in obese children and adolescents after previous weight reduction with a lifestyle intervention: maintain - paediatric part - a RCT from 2009-15. BMC Obes. 2016 Jun 10;3:29. doi: 10.1186/s40608-016-0110-8. eCollection 2016.
- Brachs M, Wiegand S, Leupelt V, Ernert A, Kintscher U, Jumpertz von Schwarzenberg R, Decker AM, Bobbert T, Hubner N, Chen W, Krude H, Spranger J, Mai K. ANP system activity predicts variability of fat mass reduction and insulin sensitivity during weight loss. Metabolism. 2016 Jun;65(6):935-43. doi: 10.1016/j.metabol.2016.03.013. Epub 2016 Apr 7.
- Weygandt M, Mai K, Dommes E, Ritter K, Leupelt V, Spranger J, Haynes JD. Impulse control in the dorsolateral prefrontal cortex counteracts post-diet weight regain in obesity. Neuroimage. 2015 Apr 1;109:318-27. doi: 10.1016/j.neuroimage.2014.12.073. Epub 2015 Jan 7.
Даты записи исследования
Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.
Изучение основных дат
Начало исследования (Действительный)
1 января 2010 г.
Первичное завершение (Действительный)
1 декабря 2015 г.
Завершение исследования (Действительный)
1 января 2016 г.
Даты регистрации исследования
Первый отправленный
17 февраля 2009 г.
Впервые представлено, что соответствует критериям контроля качества
24 февраля 2009 г.
Первый опубликованный (Оценивать)
25 февраля 2009 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
17 января 2018 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
12 января 2018 г.
Последняя проверка
1 января 2018 г.
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- EA2/017/09
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
НЕТ
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .