Skip to content

Benefits of Almond Consumption in Modulation of Intestinal Microbiome and Novel Disease Risk Biomarkers

Benefits of Almond Consumption in Modulation of Intestinal Microbiome and Novel Disease Risk Biomarkers: A Randomized Controlled Dietary Intervention Trial

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03327441
Enrollment
38
Registered
2017-10-31
Start date
2018-02-01
Completion date
2019-08-31
Last updated
2023-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Microbiota

Brief summary

The overall goal is to assess the health benefits of almond consumption on gut microbiome patterns and their association with circulating disease risk biomarkers, as well as the processes that control those pathways. Health benefits will be assessed relative to a omelette control.

Detailed description

Men and women with elevated waist circumference aged between 18-75 yrs will be recruited from the Winnipeg (Manitoba, Canada) area to participate in a two arm crossover, randomized study; each treatment period will be 4 weeks in length, with a 4 week washout period separating each treatment. Participants will be randomized to consume either i) almonds, or ii) omelettes at 15% of energy. Each of the treatment products will contain equal levels of calories.

Interventions

OTHERAlmonds

Almonds will be provided as 15% energy

OTHEROmelette

Omelettes will be provided as 15% energy

Sponsors

Almond Board of California
CollaboratorOTHER
University of Manitoba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Able to give written informed consent * Men and women 18-75 yr * Elevated waist circumferences (women greater than or equal to 80 cm, men greater than or equal to 94 cm) * LDL-C greater than or equal to 2.8 mmol/L, or less than or equal to 4.9 mmol/L * Non-smokers * Possess a telephone or email address to enable regular contact * Able to read, write and speak English

Exclusion criteria

* Pregnant female, or planning to become pregnant during the study period * Weight gain or loss of at least 10lbs in previous three months * Allergic to almonds, eggs, milk * Exercising \> 15 miles/wk or 4,000 kcal/wk * Those currently taking (or have taken within the past 3 months) lipid-lowering medications (i.e., statins) * Those currently taking (or have taken within the last 3 months) lipid-lowering supplements (i.e., omega-3 supplements, plant sterols/stanol foods and/or supplements, fibre, etc.) * Those currently taking (or have taken within the last 3 months) probiotic supplements and foods containing added probiotics (i.e., kefir, Activia, Kashi: Vive Probiotic Digestive Wellness Cereal) * Previous history of diabetes, hypertension, gastrointestinal disease, liver or lung disease or cancer, hyperthyroidism or hypothyroidism, or lung disease. * Alcohol use of \>2 drinks/day

Design outcomes

Primary

MeasureTime frameDescription
Gastrointestinal microbiome4 weeksBacterial community alpha-diversity measured using richness and diversity indices including Chao1, Shannon, Inverse Simpson. Bacterial community beta-diversity measured using weighted and unweighted UniFrac distances. The most abundant Operational Taxonomic Units (OTUs) within the bacterial community identified based on the relative abundances of the OTUs within the community. Bacterial community composition at the phylum and genus levels described based on the relative abundances of each taxa within the community. Bacterial community functional capacity measured based on the relative abundances of collected predicted functions of the community members. Ecological relationships between members of bacterial community assessed using correlation network modelling to identify keystone and foundation members of the bacterial community that have the highest number of positive (supportive) or negative (suppressive) connections (\>15) with other members of community.

Secondary

MeasureTime frameDescription
Blood total cholesterol4 weeks
Blood low-density lipoprotein cholesterol4 weeks
Blood high-density lipoprotein cholesterol4 weeks
Blood triglycerides4 weeks
Interferon gamma4 weeks
Interleukin 1 beta4 weeks
Interleukin 64 weeks
Tumor necrosis factor alpha4 weeks
Serum amyloid A4 weeks
C-reactive protein4 weeks
Vascular cell adhesion molecule 14 weeks
Intercellular adhesion molecule 14 weeks
7α-hydroxy-4-cholesten-3-one4 weeks
Fecal short chain fatty acids4 weeks
Fatty acid synthesis rate4 weeks
Cholesterol synthesis rate4 weeks
Cholesterol absorption rate4 weeks
Body mass index4 weeksWeight and height will be combined to report BMI in kg/m\^2
Waist circumference4 weeks
Hip circumference4 weeks
Blood pressure4 weeks

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026