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Assess the Effects of Replacing Foods High in Refined Carbohydrates With Avocado on Biomarkers of Inflammation.

Effects of Avocado Consumption on Inflammation and Insulin Sensitivity in Adults With Elevated High Sensitivity-C-reactive Protein (Hs-CRP): A Randomized, Controlled Crossover Trial

The objective of this trial is to assess the effects of replacing foods high in refined carbohydrates, particularly added sugars, with avocado (isocaloric substitution) on biomarkers of inflammation and insulin sensitivity in adults with elevated hs-CRP and central adiposity. Eligible participants will complete two 4-week interventions (1 avocado/d and control) separated by a 2-week washout phase. Participants will complete a total of 7 clinic visits including one screening visit (visit 1, -7 days), one baseline visit (visit 2, day 0), two visits during each 4-week diet condition (visit 3 & 6 on day 21 and visits 4 & 7 on day 28), and one visit at the conclusion of the washout phase/start of the second condition (visit 5, day 0).

調査の概要

研究の種類

介入

入学 (推定)

38

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

研究場所

    • Illinois
      • Chicago、Illinois、アメリカ、60616
        • 募集
        • Illinois Institute of Technology
        • コンタクト:
    • Nevada
      • Las Vegas、Nevada、アメリカ、89154
        • まだ募集していません
        • University of Nevada, Las Vegas
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  1. Male or female 21 - 74 years of age, inclusive;
  2. Baseline hs-CRP ≥2 to <10 mg/L;
  3. Central adiposity (waist circumference ≥35 inches in women and ≥40 inches in men);
  4. Body mass index 25.0 to 39.9 kg/m2;
  5. Normally active and judged by the Investigator to be in generally good health, based on medical history and screening measurements;
  6. Willing to consume daily study foods during each diet condition;
  7. Willing to maintain his/her regular physical activity pattern throughout the study period;
  8. Willing to follow test day instructions (refrain from consumption of alcoholic beverages and participation in vigorous physical activity for 24 hours and tobacco and caffeine for 1 hour prior to each test visit);
  9. No plans to change smoking, vaping, or other nicotine use habits during the study period; and
  10. Premenopausal women that are not using hormonal contraceptives must have a history of regular menstrual cycles (21-35 days per cycle) for at least 3 months prior to visit 1;
  11. Understands the study procedures and signs forms documenting informed consent to participate in the study and authorization for release of relevant protected health information to the study Investigator and is willing to complete study procedures.

Exclusion Criteria:

  1. Calculated energy needs of <1800 kcal/d per the Mifflin-St. Jeor Equation, with an adjustment for energy expended in physical activity;
  2. Known metabolic disease (e.g., type 1 or type 2 diabetes, metabolic dysfunction-associated steatohepatitis, etc.);
  3. Laboratory test result(s) of clinical significance based on the judgment of the Principal Investigator or qualified designee, including fasting glucose ≥126 mg/dL;
  4. Positive urine test for illicit drugs at visit 1;
  5. Clinical atherosclerotic disease;
  6. History or presence of clinically significant gastrointestinal, endocrine, renal, hepatic, hematologic, immunologic, dermatologic, pulmonary, pancreatic, neurologic, psychiatric, inflammatory or biliary disorder that, in the opinion of the Investigator, could interfere with the interpretation of the study results;
  7. History of cancer in the prior 2 years, except for non- melanoma skin cancer or carcinoma in situ of the cervix;
  8. Uncontrolled hypertension (systolic blood pressure ≥160 mm Hg and/or diastolic blood pressure ≥100 mm Hg) at screening;
  9. Unstable use (defined as initiation or change in dose) of anti-hypertensive medication within 4 weeks of visit 1;
  10. Unstable use (defined as initiation or change in dose) of thyroid hormone replacement medication within 12 weeks of visit 1;
  11. Use of beta-adrenergic blockers and/or high-dose (>25 mg/d) thiazide diuretics within 4 weeks of visit 1;
  12. Use of diabetes medications including glucagon-like peptide-1 (GLP-1) receptor agonists, GLP-1/glucose-dependent insulinotropic polypeptide (GIP) receptor agonists, alpha-glucosidase inhibitors, biguanides and biguanide combinations, thiazolidinediones, dipeptidyl peptidase-4 (DPP-4) inhibitors, meglitinides and sulfonylureas and combination sulfonylureas within 4 weeks of visit 1;
  13. Unstable use (defined as initiation or change in dose, agent, or regimen) of statins within 4 weeks of visit 1;
  14. Use of lipid-altering drugs other than statins including, but not limited to bile acid sequestrants, cholesterol absorption inhibitors, or fibrates within 4 weeks of visit 1;
  15. Use of any prescription medication with known effects on inflammation (e.g., colchicine, systemic corticosteroids) within 4 weeks of visit 1;
  16. Frequent use (≥4 doses/week) of non-steroidal anti-inflammatory drugs (NSAID) within 2 weeks of visit 2;
  17. Use of weight-loss drugs (including over-the-counter medications and/or supplements) or participation in a structured weight loss program within 4 weeks prior to visit 1;
  18. Unstable use (initiation or change in dose) within 4 weeks of visit 1 of sex hormones. Multiphasic hormonal contraceptives in which the amount of sex hormone in the active pill varies by week (i.e., biphasic, triphasic, quadriphasic) are considered unstable doses of sex hormones and are exclusionary;
  19. History of bariatric surgery or plans to have any surgery during the study;
  20. History of any major trauma or major surgical event within 2 months of visit 1;
  21. Use of herbs or dietary supplements that may affect lipid metabolism, including but not limited to omega-3 fatty acid supplements with >500 mg of eicosapentaenoic acid (EPA) and/or docosahexaenoic acid (DHA), niacin (or its analogs) at doses >200 mg/d, sterol/stanol products, dietary fiber supplements, red rice yeast supplements, garlic supplements, and soy isoflavone supplements within 2 weeks of visit 2;
  22. Use of herbs and dietary supplements that may affect carbohydrate metabolism, including chromium picolinate, ginseng, cinnamon (as a supplement) and starch blockers within 2 weeks of visit 2;
  23. Recent weight change of ±4.5 kg (~10 lbs.) within 3 months prior to visit 1;
  24. Has signs and symptoms of an active infection of clinical significance or has taken antibiotics within 5 days prior to any visit (washout is permitted by re-scheduling of the clinic visit);
  25. Extreme dietary habits (e.g., vegan, very low carbohydrate);
  26. History of an eating disorder (e.g., anorexia, bulimia nervosa, or binge eating) either diagnosed by a health professional or self-reported;
  27. Female who is pregnant, planning to be pregnant during the study period, lactating, or is of childbearing potential and is unwilling to commit to the use of a medically approved form of contraception throughout the study period;
  28. Known allergy, sensitivity, or intolerance to any components of the study foods;
  29. Exposed to any non-registered drug product within 4 weeks of visit 1;
  30. Currently participating in another research study;
  31. Use of hemp/marijuana products within 12 months of visit 1. Occasional use (e.g., once or twice a month) within 12 months of visit 1 is allowed but requires at least a 14-day washout prior to visit 2 and the participant must be willing to refrain from use during the study;
  32. Current or recent history (past 12 months of screening) or strong potential for illicit drug or alcohol abuse. Alcohol abuse will be defined as >14 drinks per week (1 drink = 12 oz beer, 5 oz wine, or 1.5 oz hard liquor); and
  33. Condition the Investigator believes would interfere with his or her ability to provide informed consent or comply with the study protocol, or which might confound the interpretation of the study results or put the person at undue risk.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:他の
  • 割り当て:ランダム化
  • 介入モデル:クロスオーバー割り当て
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
実験的:Avocado Group
1 avocado/day provided by 3 servings study products per day (muffins and pudding)
Active foods will provide the equivalent of one medium to large avocado/day in foods such as muffins and pudding, where avocado replaces refined carbohydrate, especially added sugars
他の:Control Group
3 study products per day will be provided with energy from avocado will be replaced with refined carbohydrate, especially added sugars
Control foods will have similar energy contents to active foods, but energy from avocado will be replaced with refined carbohydrate, especially added sugars.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Composite measure of inflammatory biomarkers
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change from baseline for a composite measure of inflammatory biomarkers including high-sensitivity C-reactive protein (hs-CRP), interleukin-6 (IL-6), interleukin-1 beta (IL-1β), interleukin-10 (IL-10), and tumor Necrosis Factor-alpha (TNF-α).
Change from baseline (day 0) to end of each condition (day 28)

二次結果の測定

結果測定
メジャーの説明
時間枠
Homeostasis model assessments of insulin resistance (HOMA-IR)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Changes in (HOMA-IR)
Change from baseline (day 0) to end of each condition (day 28)
Homeostasis model assessments of β-cell function (HOMA-B)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Changes in HOMA-B
Change from baseline (day 0) to end of each condition (day 28)
Matsuda index of insulin sensitivity
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in Matsuda index of insulin sensitivity
Change from baseline (day 0) to end of each condition (day 28)
Disposition index
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in disposition index
Change from baseline (day 0) to end of each condition (day 28)
high sensitivity C-reactive protein (hs-CRP)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in hs-CRP
Change from baseline (day 0) to end of each condition (day 28)
Interleukin-6 (IL-6)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in IL-6
Change from baseline (day 0) to end of each condition (day 28)
Interleukin-1 beta (IL-1β)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in IL-1β
Change from baseline (day 0) to end of each condition (day 28)
Interleukin-10 (IL-10)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in IL-10
Change from baseline (day 0) to end of each condition (day 28)
Tumor Necrosis Factor-alpha (TNF-α)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in TNF-α
Change from baseline (day 0) to end of each condition (day 28)
Fibrinogen
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in fibrinogen
Change from baseline (day 0) to end of each condition (day 28)
Soluble Intercellular Adhesion Molecule-1 (sICAM-1)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in sICAM-1
Change from baseline (day 0) to end of each condition (day 28)
Soluble Vascular Cell Adhesion Molecule-1 (sVCAM-1)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in sVCAM-1
Change from baseline (day 0) to end of each condition (day 28)
Total Cholesterol
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in total cholesterol
Change from baseline (day 0) to end of each condition (day 28)
Low-density lipoprotein cholesterol (LDL-C)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in LDL-C
Change from baseline (day 0) to end of each condition (day 28)
High-density lipoprotein cholesterol (HDL-C)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in HDL-C
Change from baseline (day 0) to end of each condition (day 28)
Non-high-density lipoprotein cholesterol (non-HDL-C)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in non-HDL-C
Change from baseline (day 0) to end of each condition (day 28)
Triglycerides
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in triglycerides
Change from baseline (day 0) to end of each condition (day 28)
Apolipoprotein B (ApoB)
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in ApoB
Change from baseline (day 0) to end of each condition (day 28)
Systolic and diastolic blood pressures.
時間枠:Change from baseline (day 0) to end of each condition (day 28)
Change in resting, seated systolic and diastolic blood pressures.
Change from baseline (day 0) to end of each condition (day 28)

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年7月2日

一次修了 (推定)

2027年2月1日

研究の完了 (推定)

2027年2月1日

試験登録日

最初に提出

2026年4月29日

QC基準を満たした最初の提出物

2026年4月29日

最初の投稿 (実際)

2026年5月5日

学習記録の更新

投稿された最後の更新 (実際)

2026年8月27日

QC基準を満たした最後の更新が送信されました

2026年8月24日

最終確認日

2026年8月1日

詳しくは

本研究に関する用語

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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