Effects of the Fos Biomedical Device on Diabetes Risk Factors and Sleep Quality in Adults at Risk for Type 2 Diabetes: A Randomized, Placebo-controlled, Crossover Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 34
- 试验地点
- 2
- 主要终点
- Glycated hemoglobin
研究概览
简要总结
Purpose Phototherapy has an array of potential benefits in human health. The effects of a non-transdermal Fos Biomedical product (which utilizes the concept of phototherapy) on diabetes risk factors and sleep quality in people at risk for type 2 diabetes are unclear. Proposed is a single-blind randomized crossover placebo-controlled trial to assess the impact of daily use of the Fos Biomedical product for a 12-week period on cardio-metabolic risk factors and self-reported sleep quality among adults at risk for type 2 diabetes.
Specific Aims
- To determine the effects of the use of the Fos Biomedical product daily for 12 weeks, as compared to placebo patch, on glycemic control in adults at risk for type 2 diabetes. Specifically, to show that the use of the Fos Biomedical product for 12 weeks, as compared to placebo patch, will improve glycated hemoglobin in adults at risk for type 2 diabetes.
- To assess the effects of the use of the Fos Biomedical product, versus placebo patch, for a 12-week period on insulin sensitivity, serum lipids, C-reactive protein, anthropometric measures, self-reported sleep quality, and endothelial function in adults at risk for type 2 diabetes. Specifically, to show clinically meaningful improvement or neutral effects in insulin sensitivity, serum lipids, C-reactive protein, anthropometric measures, self-reported sleep quality, and endothelial function in adults at risk for type 2 diabetes.
- To assess the impact of Fos Biomedical product on liver function and kidney function in adults at risk for type 2 diabetes
Hypotheses
- Daily use of the Fos Biomedical product for 12 weeks will improve glycated hemoglobin in adults at risk for type 2 diabetes.
- Daily use of the Fos Biomedical product for 12 weeks will improve or have neutral effects on insulin sensitivity, serum lipids, C-reactive protein, anthropometric measures, self-reported sleep quality and endothelial function in adults at risk for type 2 diabetes.
- The use of the Fos Biomedical product will have no clinically meaningful adverse effects on liver function and kidney function in adults at risk for type 2 diabetes.
详细描述
Background Pre-diabetes is a serious medical condition associated with elevated blood glucose that is higher than normal, but not high enough to be considered for a diagnosis of diabetes. An estimated 88 million adults aged 18 years and older have pre-diabetes in the United States (U.S.), yet more than 84% of those with pre-diabetes are unaware. Those with pre-diabetes are at increased risk for developing diabetes, cardiovascular disease (CVD), and stroke. Fifteen to 30% of individuals with pre-diabetes are likely to develop type 2 diabetes mellitus (T2DM) within 5 years. Pre-diabetes is a major risk factor associated with metabolic syndrome. Insulin resistance and excess body weight are common in both pre-diabetes and metabolic syndrome.
Metabolic syndrome - a cluster of risk factors that increase the risk of T2DM and CVD - affects about 35% of adults in the U.S. The risk factors for metabolic syndrome include hypertension, dyslipidemia, hyperglycemia, and excess body weight (especially due to excess central body fat). These risk factors represent an independent risk for developing T2DM, CVD, and stroke, as well as an increased risk of mortality. The risk of T2DM, CVD, and stroke increases with the number of metabolic risk factors. Persons with metabolic syndrome, when compared with healthy persons, have a 5-fold increased risk for T2DM. The combination of pre-diabetes and metabolic syndrome compared with healthy persons is associated with an even higher (i.e., 21-fold) risk for T2DM.
An inconsistent sleep schedule or a general lack of sleep has been associated with increased risk of developing T2DM. Specifically, sleep disturbance is associated with pre-diabetes and metabolic syndrome. Sleep disturbance is associated with poor cardio-metabolic control (i.e., hypertension, dyslipidemia, and a reduction in insulin level released after eating). Further, elevated stress hormones that keep the body awake have been associated with increased blood glucose level by increasing the production of glucose in the liver; decreasing glucose uptake in the muscles and fat cells; decreasing insulin secretion; and increasing insulin resistance. In addition, sleep deprivation has also been associated with increased appetite, which heightens the risk of T2DM. Again, insufficient sleep has been associated with higher levels of ghrelin, which increase appetite, and lower levels of leptin, which signals fullness. Therefore, improving sleep patterns has the potential to improve cardio-metabolic risk factors among those at risk for T2DM.
Lifestyle practices that promote good sleep hygiene and reduce stress have been associated with lower risk of T2DM and the control of cardio-metabolic risk factors among those at risk for T2DM. In addition, consistent sleep patterns have also been associated with improved glycemic control in T2DM. Phototherapy is thought to help improve sleep patterns in persons with circadian rhythm sleep disorders to normal sleeping patterns and times. Further, in a meta-analysis phototherapy therapy was shown to improve symptoms of vascular complications and quality of life that are linked to diabetes. In animal models, phototherapy has been shown to reduce abdominal fat. In addition, phototherapy has also been associated with improved insulin sensitivity in T2DM.
Phototherapy, also known as photobiomodulation (PBM), or low-level light therapy, has been known for almost 50 years but still has not gained widespread acceptance, largely due to uncertainty about the mechanisms of action. In recent years, much knowledge has been gained in this area. The primary site of light absorption in mammalian cells has been identified as the mitochondria, and more specifically, cytochrome c oxidase (CCO), an enzyme that contains both heme and copper centers and is known to reduce oxygen to water at the end of the mitochondrial respiratory chain. CCO has recently been shown to have an additional enzymatic activity: the reduction of nitrite to nitric oxide (NO) upon exposure to low-intensity light. The absorption peaks of CCO are in the visible (420-450 nm and 600-700 nm) and the near-infrared (760-980 nm) spectral region.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Prevention
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
盲法说明
The investigators and study participants will be blinded to treatment assignments. Each of the two patch products (Fos Biomedical product and placebo) will be provided to the study team by the study funder (Fos Biomedical). The products will have a similar appearance and texture. One will be described to study participants and study team members as "Product A" and the other as "Product B." The description of products A and B will be sent by Fos Biomedical in a sealed envelope that will be kept in locked cabinet at the PRC. The envelope will be opened at the conclusion of the statistical analyses. Therefore all members of the investigative team will be blinded to the study interventions.
入排标准
- 年龄范围
- 40 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •(1) Males > 40 years of age; (2) Post-menopausal females not currently on hormone replacement therapy; (3) Non-smokers; (4) Overweight with BMI ≥25kg/m²; (5) At risk for type 2 diabetes as defined by meeting at least one of the criteria listed below: (i) Metabolic syndrome, i.e. meet three out of five of the following criteria:
- •Blood pressure >130/85 mmHg or currently taking antihypertensive medication;
- •Fasting plasma glucose (FPG) >100 mg/dL (6.1 mmol/L);
- •Serum triglycerides level (TG)>150 mg/dL (1.69 mmol/L);
- •High-density lipoprotein (HDL) cholesterol level < 40 mg/dL (1.04 mmol/L) in men, and < 50 mg/dL (1.29 mmol/L) in women;
- •Waist circumference of >40 inches (102 cm) for men and > 35 inches (88 cm) for women; fasting blood glucose >100mg/dL and <126mg/dL.
- •(ii) Hemoglobin A1C in the range of 5.7-6.4%
排除标准
- •Failure to meet inclusion criteria;
- •Anticipated inability to complete study protocol for any reason;
- •Type 1 or type 2 diabetes;
- •Personal history or family history of skin cancer;
- •Having lupus;
- •Having liver disease;
- •Use of lipid-lowering or antihypertensive medications, unless stable on medication for at least 3 months and willing to refrain from taking medication for 12 hours prior to clinical outcome measures assessment;
- •Regular use of high doses of vitamin E or C;
- •Use of insulin, glucose-sensitizing medication, vasoactive medication (including glucocorticoids, antineoplastic agents, psychoactive agents, or bronchodilators) or nutraceuticals;
- •Regular use of fiber supplements;
- •Sleep apnea;
- •Coagulopathy, known bleeding diathesis, or history of clinically significant hemorrhage; or current use of warfarin.
- •Known allergic or dermatological reactions to any of the components of the patch product or placebo - polyethylene, silicone, or acrylate adhesive - that could have contact with the skin of study participants during their use of the product.
结局指标
主要结局
Glycated hemoglobin
时间窗: Baseline, 12 weeks, 20 weeks, 32 weeks
Glycated hemoglobin (HbA1c) will be measured to assess the average concentration. HbA1c predicts the average amount of plasma glucose. The study team will use HbA1c to gauge the average amount of blood glucose level over a previous 3-month period.
次要结局
- C-reactive protein (CRP)(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Pittsburgh Sleep Quality Index (PSQI)(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Body mass index (BMI)(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Percent body fat(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Visceral fat rating(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Total body water percent(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Kidney function(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Insulin sensitivity(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Office blood pressure (BP)(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Endothelial function (EF)(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Physical activity(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Medication use(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Body weight(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Waist circumference(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Serum lipids(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Dietary pattern(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Liver function(Baseline, 12 weeks, 20 weeks, 32 weeks)
- Compliance(Baseline, 12 weeks, 20 weeks, 32 weeks)