NCT04291391Completed
The Alberta NutrIMM Study - Nutrition and Immunity
The Alberta NutrIMM (Nutrition and Immune Function) Study: Establishing the Importance of Diet and Insulin Resistance in Modulating Immune Function in Obesity
Source: ClinicalTrials.gov · Last updated 6 Feb 2024
Brief summary (registry, in English)
This study will investigate the effect of body weight, diet, and high blood sugar levels, under controlled feeding conditions, on immune function in individuals with and without obesity. This study will be a non-randomized, four-arm parallel group, clinical trial under controlled feeding conditions (4-week nutritional intervention using a North American-type diet). A sample size of n=128 participants will be allocated into one of the following groups: * Individuals without obesity and normoglycemia (NG) (Lean-NG) * Individuals with obesity and normoglycemia (Obese-NG) * Individuals with obesity and glucose intolerance (GI) (Obese-GI) * Individuals with obesity and type 2 diabetes (T2D) (Obese-T2D) The following outcomes will be analyzed: * Immune cell function (ex-vivo cytokine production after stimulation with mitogen and T cell proliferation); * Immune cell phenotypes; * Systemic inflammation (C-reactive protein and plasma cytokines); * Glucose, insulin, glycated hemoglobin (HbA1c), and lipids; * Fatty acids and phospholipds composition in plasma and red blood cells membrane.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 114 (actual)
- First submitted
- 29 Nov 2019
- Start date
- 1 Sept 2019
- Primary completion date
- 16 May 2023
- Lead sponsor
- University of Alberta
- Diseases
- Obesity, Type 2 diabetes
- NCT number
- NCT04291391
What you commit to
- Study type: Interventional
- Participants enrolled: 114
- From 1 Sept 2019 to the primary completion date, 16 May 2023
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Diseases known to affect the immune system, such as infectious, inflammatory, and autoimmune diseases or autoimmune-related or suspected conditions (e.g., T1D, systemic lupus erythematosus, inflammatory bowel disease), except for psoriasis, atopic dermatitis, and rheumatoid arthritis. Continuous use of anti-inflammatory or immunosuppressant drugs and supplements for which washout is not possible, except for medications which participants with obesity could not refrain from (e.g., baby aspirins);
Other illness
- Current or recent history cardiovascular diseases or events (e.g., ischemic, rheumatic, or congenital heart disease, stroke, peripheral vascular disease, heart failure, familial hypercholesterolemia or other monogenic dyslipidemia), use of cardiac implantable electronic devices;
- Current or recent cancer, including remission, during the last five years;
- Renal disorders, endocrine disorders other than T2D (e.g., acromegaly, Addison's disease, Cushing's disease);
- Untreated or uncontrolled thyroid diseases (e.g., Hashimoto's disease, hypothyroidism, hyperthyroidism);
- Known allergy, aversion to any components of the menu, or restricted dietary patterns (e.g., gluten-free diet, vegetarianism, kosher or halal diets) for which accommodations within the menu are not possible;
Lab values
- Participants under titration of their medication or initiating a new treatment or HbA1c \>10.5%;
Other
- Women who are pregnant or plan to become pregnant during the study duration, who are lactating, who have an irregular menstrual cycle or are in perimenopause;
- Regular use of cannabis (e.g. smoking);
- Taking part in any other intervention study that might affect the outcomes of the current study.
Who the study is looking for
- Age of 18 years to 70 years;
- Body weight stable (± 3%) for at least three months prior to study commencement;
- Body mass index (1) between 18.5 and 24.9 (± 0.5) kg/m2 or (2) between 30 and 50 kg/m2 (± 0.5) kg/m2 or waist circumference \>88 cm or \> 102 cm for females and males, respectively;
- See below for specific group allocation criteria based on glucose, HbA1c, High density lipoprotein cholesterol (HDL-C), and triglycerides.
- Fasting blood glucose levels (mmol/L): \< 5.6 (Lean-NG and Obese-NG), 5.6-6.9 (Obese-GI), and ≥ 7.0 (Obese-T2D);
- HbA1c (%): \< 5.5 (Lean-NG and Obese-NG), 5.5-6.4 (Obese-GI), and ≥ 6.5 (Obese-T2D);
- Blood Pressure (mmHg): \< 130/85 (Lean-NG and Obese-NG), not required for Obese-GI and Obese-T2D;
- Triglycerides (mmol/L): \< 1.7 (Lean-NG and Obese-NG), not required for Obese-GI and Obese-T2D;
- HDL-C (mmol/L): ≥ 1.03 for males and ≥ 1.29 for females (Lean-NG and Obese-NG), not required for Obese-GI and Obese-T2D.
Age in the registry: 18 years to 70 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Alberta Coordinator of this site? Confirm its status | Edmonton | Canada | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.