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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).

Studieoversigt

Status

Rekruttering

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

38

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

    • Illinois
      • Chicago, Illinois, Forenede Stater, 60616
        • Rekruttering
        • Illinois Institute of Technology
        • Kontakt:
    • Nevada
      • Las Vegas, Nevada, Forenede Stater, 89154
        • Ikke rekrutterer endnu
        • University of Nevada, Las Vegas
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Beskrivelse

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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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
Andet: 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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Composite measure of inflammatory biomarkers
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Homeostasis model assessments of insulin resistance (HOMA-IR)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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.
Tidsramme: 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)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

2. juli 2026

Primær færdiggørelse (Anslået)

1. februar 2027

Studieafslutning (Anslået)

1. februar 2027

Datoer for studieregistrering

Først indsendt

29. april 2026

Først indsendt, der opfyldte QC-kriterier

29. april 2026

Først opslået (Faktiske)

5. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

27. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

24. august 2026

Sidst verificeret

1. august 2026

Mere information

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