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临床试验/NCT06605898
NCT06605898招募中不适用

Optimized Tailored Interventions in Metabolic and Lifestyle Outcomes: Examining the Effects of the Mediterranean-DASH Intervention for Neurodegenerative Delay(MIND) on Cognitive Performance, Metabolic Health and Lifestyle Outcomes Using Advanced Machine Learning Strategies

University of Illinois at Urbana-Champaign1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2024年7月3日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
72
试验地点
1
主要终点
Fasting Blood Glucose

研究概览

简要总结

The goal of this clinical trial is to learn if increasing adherence to a Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet pattern improves brain and heart health relative to a healthy control diet in middle-aged adults. Our research team will evaluate three different groups: the first group will be chosen using a predictive analytics model that predicts who will benefit most from the MIND diet, the second group will follow the MIND diet without being pre-selected, and the third group will eat a standard healthy diet to serve as a comparison.

The main questions it aims to answer are:

Does the MIND diet improve cognitive performance and heart health relative to a control diet? How does the health impact of the MIND diet in participants pre-identified through predictive analytics compare to those without such pre-selection? Which of the three groups - predictive analytics selected MIND diet group, standard MIND diet group, or healthy control - demonstrate the most significant improvements in cognitive and cardiovascular health over the course of the trial?

Participants will:

Consume one meal that follows the MIND diet or a control meal every day for 3 months. Visit the lab before and after the 3 months of meals for tests. Keep a record of the food they eat during the study.

详细描述

The purpose of this study is to understand how a healthy diet is related to thinking ability and heart health. Participants will be asked to consume a microwaveable study meal or prepackaged smoothie every day for 12 weeks. These meals will be delivered to participant homes using Daily Harvest meal delivery service. The study meals and smoothies will follow either a dietary pattern thought to improve brain and heart health (MIND), or a control diet, and will include foods commonly found in grocery stores. Participants will not know which diet they are assigned to (active or control). Participants will also be asked to follow simple dietary guidance on a healthy diet in addition to the meals provided. Participants will complete a series of online forms or surveys. Additionally, participants will come to 4 in-person laboratory visits to complete several computer-based tests of memory and attention while wearing an EEG cap. Participants will also be asked to complete an eye test, a heart rate and blood pressure assessment, a bone and body scan called DXA, and a blood draw at the beginning of the study and again at the end of the 12-week diet period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Participant)

入排标准

年龄范围
45 Years 至 64 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •45-64 years of age
  • •20/20 or corrected vision
  • •No food allergies or intolerances
  • •Not pregnant, lactating, or have given birth in the past 12 months
  • •Do not smoke, use tobacco, or abuse drugs
  • •Absence of liver or gastrointestinal diseases (i.e., primary biliary cirrhosis or gallbladder disease, chronic constipation, diarrhea, Crohn's disease, celiac disease, ulcerative colitis, irritable bowel syndrome, diverticulosis, stomach or duodenal ulcers), hepatitis, HIV, and cancer
  • •Not currently taking oral hypoglycemic agents, or insulin
  • •No history of malabsorptive or bariatric surgery
  • •Cognitively intact with no prior diagnosis of neurological disease (i.e., mild cognitive impairment, Alzheimer's disease, vascular dementia, and/or Asperger's syndrome)
  • •Able to consume the study meals
  • •Not enrolled in another dietary, exercise, or medication study during the study.

排除标准

  • •Non-consent of participant
  • •Above 64 or below 45 years of age
  • •Vision not 20/20 or corrected
  • •Food allergies or intolerances
  • •Pregnant, lactating, or have given birth in the past 12 months
  • •Smoke, use tobacco, or abuse drugs
  • •Prior diagnosis of liver or gastrointestinal disease (i.e., primary biliary cirrhosis or gallbladder disease, chronic constipation, diarrhea, Crohn's disease, celiac disease, ulcerative colitis, irritable bowel syndrome, diverticulosis, stomach or duodenal ulcers), hepatitis, HIV, or cancer
  • •Currently taking oral hypoglycemic agents or insulin
  • •History of malabsorptive or bariatric surgery
  • •Cognitively impaired and/or prior diagnosis of neurological disease (i.e., mild cognitive impairment, Alzheimer's disease, vascular dementia, and/or Asperger's syndrome)
  • •Unable to consume the study meals
  • •Concurrent enrollment in another dietary, exercise, or medication study

研究组 & 干预措施

Standard MIND diet

Experimental

Participants in the active MIND diet group will be asked to consume one ready-to-eat meal per day from Daily Harvest® meal delivery service. This will be a standard treatment arm without prior selection through predictive analytics. The treatment meals will follow MIND diet guidelines and include leafy green vegetables, nuts, legumes, whole grains, berries, and extra virgin olive oil.

干预措施: MIND Diet (Other)

Predictive Analytics informed MIND Diet

Experimental

Participants in the active MIND diet group informed by predictive analytics will be pre-identified based on the results of a machine learning model that predicts who will most likely benefit from the MIND diet. The participants in this group will be asked to consume one ready-to-eat meal per day from Daily Harvest® meal delivery service. The treatment meals will follow MIND diet guidelines and include leafy green vegetables, nuts, legumes, whole grains, berries, and extra virgin olive oil.

干预措施: MIND Diet (Other)

Control Diet

Active Comparator

Participants in the control diet group will be asked to consume one ready-to-eat meal per day from Daily Harvest® meal delivery service. The Control group will receive daily meals that are isocaloric with the active/experimental meals but will follow a general diet based on the average American diet and Dietary Guidelines for Americans (i.e., vegetables, fruits, nuts, whole grains, and unsaturated fats).

干预措施: Control Diet (Other)

结局指标

主要结局

Fasting Blood Glucose

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in fasting blood glucose concentration (mg/dL) between groups.

Attentional Accuracy

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in accuracy (%) between groups using a computerized flanker task.

Attentional Reaction Time

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in reaction time (ms) between groups using a computerized flanker task.

Attentional Resource Allocation

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in P3 event related potential amplitude (microvolts) between groups using a computerized flanker task.

Attentional Processing Speed

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in P3 event related potential latency (ms) between groups using a computerized flanker task.

Fasting Blood Triglycerides

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in fasting blood triglyceride concentration (mg/dL) between groups.

Fasting Blood HDL

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in fasting blood HDL concentration (mg/dL) between groups.

Blood Pressure

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in systolic and diastolic blood pressure (mmHg) between groups

Waist Circumference

时间窗: [Time Frame: 12 weeks (Baseline vs Follow-Up)]

Changes in waist circumference (cm) between groups.

次要结局

  • Macular Pigment Optical Density([Time Frame: 12 weeks (Baseline vs Follow-Up)])
  • Visceral Adipose Tissue([Time Frame: 12 weeks (Baseline vs Follow-Up)])

研究者

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

Naiman Khan

Associate Professor

University of Illinois at Urbana-Champaign

研究点 (1)

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