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临床试验/NCT06152588
NCT06152588招募中不适用

Restricted Eating Time in the Treatment of Type 2 Diabetes - the RESET2 Trial.

Steno Diabetes Center Copenhagen2 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2024年3月21日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
160
试验地点
2
主要终点
Change in HbA1c (mmol/mol)

研究概览

简要总结

The overall aim of the present study is to investigate the effectiveness of implementing a 1-year time-restricted eating (TRE)-based intervention on glycaemic control, body weight and composition, cardiometabolic risk factors, and behaviour in individuals with overweight/obesity and type 2 diabetes (T2D).

详细描述

In people with type 2 diabetes (T2D), weight loss is associated with improved glycaemic control and markers of cardiometabolic function as well as reduced use of antidiabetic medicine. Beyond pharmacological treatments, current strategies to reduce body weight and improve glycaemia include energy-restricted diets and increased physical activity.

Lifestyle interventions are complex, affecting many aspects of peoples' daily life. Dietary restrictions often result in rapid weight loss but the weight is gradually regained by many. Barriers to implement and maintain dietary changes include relapse of old habits and lack of knowledge, support, and insights into the type and amount of foods eaten. Previous lifestyle interventions targeting weight loss in T2D show efficacy for improving markers of metabolic and cardiovascular risk, including body weight and glycaemia during the intervention, but weight regain is often present. One reason may be that the intervention is not modified according to the needs of the target group. Often, weight loss interventions are shaped by a 'one size fits all' approach where both individual capabilities and motivation as well as social and contextual factors are more or less ignored. A user-based design could facilitate enrolment of participants and promote implementation and maintenance of the intervention among participants.

Intermittent fasting regimens have been suggested as efficient strategies for improving cardiometabolic health to a greater extent than can be attributed to the reduction in energy intake alone. TRE limits the time available for food intake to typically 8-10 hours/day without other dietary restrictions and has been put forward as a novel, acceptable, and safe strategy that has shown promising effects on body weight, glucose metabolism, appetite, and cardiometabolic health in individuals at high risk of T2D.

Although it has been suggested that TRE is a safe and feasible intervention, the longer-term effectiveness of TRE on glycaemic control and weight loss in individuals with T2D is unknown alongside the long-term acceptability and sustainability. Additionally, potential social and contextual challenges associated with integration of TRE into ordinary daily life structure and routines call for new approaches to support the individual in implementing and maintaining the strategy.

Overall, the RESET2 study consists of three phases; 1) Need assessment, 2) Pilot study, and 3) RCT. The aim of the present study (RCT) is to investigate the effectiveness of implementing a 1-year TRE-based intervention in individuals with overweight/obesity and T2D. Participants will attend 6 visits at Steno Diabetes Center Copenhagen (SDCC): Visit 0 (screening), Visit 1 (baseline, minimum 10 days after screening), Visit 2 (10 days prior to visit 3), Visit 3 [3 months (12 weeks) after baseline], Visit 4 (10 days prior to visit 5), Visit 5 [12 months (52 weeks) after baseline].

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: ≥18 years
  • Overweight or obesity (BMI ≥25 kg/m2)
  • T2D with HbA1c>53 mmol/mol
  • Habitual eating window ≥12 h/day (incl. foods/snacks and energy-containing beverages)

排除标准

  • Bariatric surgery or planned bariatric surgery within study duration
  • Use of fast acting insulin and combination insulin products
  • Habitual CGM use
  • A wish to adhere to Ramadan
  • For women: current/planned pregnancy or lactation
  • Alcohol or drug abuse (judged by investigator) or treatment with disulfiram
  • Severe hypoglycaemia within last year (Severe hypoglycaemia, as defined by the American Diabetes Association (ADA), denotes severe cognitive impairment requiring external assistance for recovery)
  • Inability to understand written and oral information in Danish
  • Unable or unwilling to adhere to TRE; for instance, due to competing medical conditions.
  • Medical condition which, based on investigators assessment, challenges participation including but not limited to severe heart, vascular or lung disease, cancer, chemotherapy, psychiatric, gastrointestinal, rheumatic, or endocrine diseases etc.
  • Concomitant participation in other intervention study
  • Inability to perform neuropsychological tests (e.g., severe vision and hearing impairment that can-not be improved with aids such as glasses and hearing aids, or language barrier.)
  • Exclusion criteria for the sub-study:
  • Magnetic resonance imaging (MRI) contraindications based on the MR department's exclusion criteria including pacemaker or other implanted electronic devices, implanted metal objects not compatible to MRI scanning and severe claustrophobia
  • Participants who do not wish to be informed about accidental findings by MR.

结局指标

主要结局

Change in HbA1c (mmol/mol)

时间窗: Change from baseline to the end of the intervention (12 months)

Assessed from blood samples in fasted state.

次要结局

  • Body weight (kg)(Change from baseline to end of the intervention (12 months). Measured at baseline, 3 months, 12 months)
  • Fat mass (kg)(Change from baseline to end of the intervention (12 months). Measured at baseline, 3 months, 12 months)
  • Time in range (% 3.9-10.0 mmol/l)(Change from baseline to end of the intervention (12 months). Measured at baseline, 3 months, 12 months)
  • Use of antidiabetic medication(Change from baseline to end of the intervention (12 months). Assessed at baseline, 3 months, 12 months.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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