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临床试验/NCT04916730
NCT04916730进行中(未招募)不适用

Effect of Time-restricted Eating on Catecholamine-sensitivity of Adipose Tissue in Obese Adults

University of California, San Diego2 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2020年12月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
61
试验地点
2
主要终点
Effects of TRE on Body Weight

研究概览

简要总结

In a randomized controlled trial, the investigators intend to measure the health impact of time-restricted eating (TRE) in obese patients (body mass index (BMI) ≥ 30 kg/m2), who habitually eat for more than 14 hours every day. Patients will be randomly assigned to a control group of behavioral nutritional counseling (standard of care) or the intervention group of behavioral nutrition counseling with the addition of adopting a 10-hour eating window for 12 weeks (TRE).

详细描述

The current worldwide epidemic of obesity puts millions of people at increased risk for cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM), and while insulin resistance has been a traditional focus of treatment, resistance to catecholamines in obesity is likely a key factor hampering weight loss efforts. Catecholamines are key drivers of lipolysis in adipose tissue and bind to beta-3 adrenergic receptors (ADRB3) on the surface of adipocytes. Chronic inflammation is characteristic of obesity and suppresses the expression of adipocyte ADRB3, increasing fat storage. This leaves adipose tissue metabolically inflexible and in a state of energy preservation instead of burning fat to promote and maintain weight loss. Thus, catecholamine resistance of adipose tissue is an important target for lifestyle and therapeutic intervention. Time-restricted eating (TRE) is a therapeutic intervention that promotes weight loss and healthier metabolism by aligning dietary intake with circadian rhythms. In this RCT, individuals with obesity will be enrolled in a 14-week study of TRE and behavioral nutritional counseling vs behavioral nutritional counseling alone. In the TRE group, dietary intake will be limited to a self-selected 10-hour window. Information will be collected about adipose tissue catabolism (lipolysis) using samples collected by adipose tissue biopsy of subcutaneous abdominal adipose tissue.

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
Single (Investigator)

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 old
  • BMI 30-50 kg/m2
  • Own a smartphone with Apple iOS or Android OS
  • Baseline eating window ≥ 14 hours/day
  • If patients are on cardiovascular medications (HMG CoA reductase inhibitors (statins), other lipid modifying drugs (including over the counter drugs such as red yeast rice and fish oil), anti-hypertensive drugs, no dose adjustments will be allowed during the study period.

排除标准

  • Taking insulin or anti-diabetic medications within the last 6 months.
  • Manifest diabetes, defined as fasting glucose ≥ 126 mg/dL, HbA1c ≥ 6.5%, or diagnosis of diabetes.
  • Currently taking any medication that is meant for, or has known effect on, appetite or body weight
  • Pregnant or breast-feeding women.
  • Caregiver for a dependent requiring frequent nocturnal care/sleep interruptions. Shift workers with variable (e.g. nocturnal) hours.
  • Planned international travel (time zone changes) during study period.
  • Taking therapeutic anticoagulation which might increase risk of bleeding from adipose tissue biopsy
  • History of surgical intervention for weight loss.
  • History of eating disorder
  • Currently enrolled in a weight-loss or weight-management program
  • On a special or prescribed diet for other reasons (e.g. Celiac disease)
  • Known inflammatory and/or rheumatologic disease
  • Active tobacco abuse or illicit drug use or history of treatment for alcohol abuse
  • History of bone marrow or solid organ transplant
  • History of heart failure
  • History of major adverse cardiovascular events (acute coronary syndrome (ACS), percutaneous coronary intervention, coronary artery bypass graft surgery, stroke/transient ischemic attack (TIA)).
  • History of atrial fibrillation or atrial flutter
  • History of malignancy, other than non-melanoma skin cancer, that is currently being treated, or that has not been treated with definitive therapy and considered to be in remission.
  • History of hypo- or hyperthyroidism requiring dose titration of thyroid replacement medication(s) within the past 3 months (i.e. hypothyroidism on a stable dose of thyroid replacement therapy is not an exclusion)
  • History of adrenal disease
  • History of cirrhosis
  • History of stage 4 or 5 chronic kidney disease or requiring dialysis
  • History of HIV/AIDS
  • Uncontrolled psychiatric disorder (including history of hospitalization for psychiatric illness).
  • History of obstructive sleep apnea (not on stable positive pressure therapy or other treatment for at least 3 months prior to enrollment)
  • Abnormal screening labs: renal dysfunction (eGFR < 30 ml/min/1.73 m2), anemia, hypo- or hyperthyroidism, coagulopathy, abnormal liver function (AST, ALT > 3x upper limit of normal)

研究组 & 干预措施

TRE + SOC

Experimental

Participants in this arm will receive standard of care nutritional behavioral counseling and will implement a daily, self-selected, 10-hour window within which they must consume all calories. They will also be required to log their caloric intake through the use of a smartphone app

干预措施: Time Restricted Eating (Behavioral)

Standard of Care (SOC)

Placebo Comparator

Participants will receive standard of care nutritional behavioral counseling and will be required to log their caloric intake through the use of a smartphone app.

干预措施: Standard of Care (Behavioral)

结局指标

主要结局

Effects of TRE on Body Weight

时间窗: Baseline to end of 12 week intervention

Measured as change in weight (kg).

次要结局

  • Effects of TRE on Body Composition(Baseline to end of 12 week intervention)

研究者

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

Michael Wilkinson

Assistant Professor of Medicine

University of California, San Diego

研究点 (2)

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