Skip to content

Chestnut Consumption on Modulation of Gut Microbiota and Metabolic Parameters

The Effect of Chestnut Consumption on Modulation of Gut Microbiota and Metabolic Parameters

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05705960
Acronym
CULTIVAR
Enrollment
33
Registered
2023-01-31
Start date
2022-11-15
Completion date
2023-03-31
Last updated
2023-01-31

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

Conditions

Diet Habit

Keywords

Chestnut, Gut microbiota diversity, Short chain fatty acid, Lipid

Brief summary

The chestnut tree (Castanea sativa Mill.) is a species widely cultivated in Portugal, which is a major producer of chestnuts. Nuts are nutritionally interesting, not only because of their content of vitamins, minerals, and phytochemicals but also of their high fiber content. Fiber, as it is not digested by humans, has a preponderant role in the intestinal microbiota, for its maintenance, and, consequently, has an impact on metabolic status. The inclusion of foods rich in these components, and with extensive local production, can be an excellent strategy for improving the metabolic parameters of the population. The main objective of this single group assignment clinical trial is to evaluate the effect of including roasted chestnuts in the daily diet on the composition and diversity of the intestinal microbiota. It is also intended to evaluate metabolic parameters to determine the impact of this intervention.

Interventions

Daily consumption of roasted chestnut (150g) for 14 days

Sponsors

Associação Centro de Apoio Tecnológico Agro-Alimentar de Castelo Branco (CATAA)
CollaboratorUNKNOWN
Universidade Nova de Lisboa
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Caucasian. * Filling informed consent. * Body mass index (BMI) between 18,5 kg/m2 and 25 kg/m2.

Exclusion criteria

* Chestnut sensibility. * Chestnut daily consumption in the month before the study initiation. * Having taken antibiotics within the 6 months prior to beginning the study; * Use of pro/prebiotics or fiber as a dietary supplement or any food/molecule that modifies intestinal transit time 6 weeks before recruitment. * Use of laxative 6 weeks before recruitment. * Specific dietary regimen (e.g., vegan). * Specific nutritional therapy (e.g. high protein). * Excessive alcohol consumption. * Smoking. * Diagnosis of gastrointestinal pathology, hormonal or thyroid pathology, autoimmune diseases, chronic use of corticosteroids, psychiatric disease or Diabetes Mellitus. * Use of proton pump inhibitors, antidiabetic drugs, insulin, or statins. * Pregnant or breastfeeding. * Participation in another clinical trial within the last 3 months.

Design outcomes

Primary

MeasureTime frameDescription
Changes in Gut microbiota characterization14 daysDifference in Gut microbiota taxonomic characterization, from baseline to the end of intervention
Changes in Gut microbiota diversity14 daysDifference in Gut microbiota Shannon index, from baseline to the end of intervention

Secondary

MeasureTime frameDescription
Changes in HOMA-IR14 daysChanges in HOMA-IR from baseline to end of intervention
Changes in total cholesterol14 daysChanges in total cholesterol, measured in mg/dL, from baseline to end of intervention
Changes in LDL cholesterol14 daysChanges in LDL cholesterol, measured in mg/dL, from baseline to end of intervention
Changes in high sensitivity PCR14 daysChanges in high sensitivity PCR, measured in mg/dL, from baseline to end of intervention
Changes in breath H214 daysChanges in breath H2, measured in ppm, from baseline to end of intervention
Changes in breath CH414 daysChanges in breath CH4, measured in ppm, from baseline to end of intervention
Changes in fecal butyrate14 daysChanges in fecal butyrate, measured in M, from baseline to end of intervention
Changes in fecal ALP14 daysChanges in fecal ALP, measured in mg/g feces, from baseline to end of intervention
Changes in fecal LPS14 daysChanges in fecal LPS, measured in EU/mL , from baseline to end of intervention
Changes in IL-1b14 daysChanges in IL1b, measured in pg/mL , from baseline to end of intervention
Changes in TNFa14 daysChanges in TNFa, measured in pg/mL , from baseline to end of intervention
Changes in adiponectin14 daysChanges in adiponectin, measured in ng/mL , from baseline to end of intervention
Changes in leptin14 daysChanges in leptin, measured in ng/mL , from baseline to end of intervention
Changes in fecal acetate14 daysChanges in fecal acetate, measured in M, from baseline to end of intervention
Changes in fasting glucose14 daysChanges in fasting glucose, measured in mg/dL, from baseline to end of intervention

Countries

Portugal

Contacts

Primary ContactAna Faria, PhD
ana.faria@nms.unl.pt00351218803033

Outcome results

None listed

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