Cognitive PerformancePEANUTYNCT06127511
Peanut Consumption on Cognitive, Weight, and Inflammation
A study testing Food (peanut) in people with Cognitive Performance and Inflammation, run by University of Barcelona at 1 site in Spain.
Trial summary
A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Read more about this study
- Who is it for?
- Ages 10 to 12 yearsHealthy volunteers can take part
- Conditions the study is for
- Cognitive Performance, Inflammation, Weight Change, Body
- What is being tested?
- Food (peanut)
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 142 participants
- Where
- 1 siteSpain
- Study dates
- 29 Jan 2024to 31 Dec 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 10 to 12 years
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- Eligible participants will be young adolescents, boys and girls, aged between 10 and 12 years who attend regular primary schools in Barcelona. The schools will assist with the participant recruitment through the classes and after that, a total of one-hundred students will be randomly included in each group. In all cases, participation will be voluntary and informed consent will be obtained prior to the study.
Who cannot join
- The exclusion criteria will be history of allergy or intolerance to peanuts, any medical conditions or dietary restrictions that would affect peanut consumption, being able to understand Spanish or Catalan, and use of antibiotics in the month prior to the study.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Peanut Consumption on Cognitive Performance, Weight Management, and Inflammation in Young Adolescents
A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Schools willing to participate will be randomly assigned to either the intervention or the control group. After the recruitment, the participants will follow a peanut-free diet for two weeks. Both arms will receive a multidimensional educational intervention designed by the Gasol Foundation to promote healthy dietary habits based on Mediterranean diet recommendations, along with exercise performance, healthy sleeping habits and emotional knowledge. Half of the participants (intervention group) will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months.
Read the detailed description
Background:
Regular nut consumption has been associated with reduced inflammation, oxidative damage, and improved vascular function, which may benefit cognitive function. Their content in phenolic acids, mainly p-coumaric and isoferulic acids may help prevent and cure diseases including Alzheimer's, diabetes, cancer, hypertension, and atherosclerosis that are associated with oxidative stress suggesting it could be used as a potential new neuroprotective tactic. Polyphenols have been shown to influence gut microbiota composition and activity, and their metabolites, including short-chain fatty acids (SCFAs), may modulate brain biochemistry by acting as neurotransmitters in the central nervous system, potentially leading to effects against depression and neurodegenerative disease.
Childhood is an important period for brain development, and nutrients aid the formation of new synaptic connections and support learning processes at school and in home environments. Adolescence is also a period where brain connectivity and complex behaviours are further refined. While a positive association has been observed between the consumption of healthy foods (fruits, vegetables, whole grains, fish, nuts, dietary fiber) and cognitive function, research on the association between nut consumption and cognitive health during adolescence is scarce.
In addition, evidence shows that incorporating peanut and peanut-based products into the diet does not lead to weight gain or higher body weight and may even promote long-term weight maintenance and increase linear growth due to their arginine content.
Due to the potential benefits of schools in preventing overweight and obesity, and the lack of research on the relationship between nut consumption and cognitive health during childhood and adolescence, the investigators plan to conduct an intervention study to investigate the association between peanut consumption and cognitive ability, weight management and inflammation in Spanish children aged 10-12 years. As the nutritional composition of peanuts can vary depending on their form, this study will examine the impact of the regular consumption of 25g of whole-skin roasted peanuts on cognitive function, mood, and school performance in healthy young adolescents.
Study design:
A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Schools willing to participate will be randomly assigned to either the intervention or the control group. After the recruitment, the participants will follow a peanut-free diet for two weeks. Both arms will receive a multidimensional educational intervention designed by the Gasol Foundation to promote healthy dietary habits based on Mediterranean diet recommendations, along with exercise performance, healthy sleeping habits and emotional knowledge. Half of the participants (intervention group) will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months.
Sample size:
Our study is designed based on previous research findings that suggest peanut consumption could influence cognitive performance and adiposity. Using a cluster design, the investigators aim to detect a significant difference of 1.3 (SD 0.8) absolute points in body mass per kJ consumed and a 6.9-unit (SD 3.1) improvement in cognitive performance score between the intervention and control groups, at a 95% confidence level, 80% power, and an estimated number of 20-40 students per school. With an intra-class correlation coefficient of 0.02, the investigators estimated a sample size of 6 schools (3 per arm) with a total of 200 participants (100 in each arm) at baseline, allowing for a 10% drop-out rate.
Ethical aspects:
The project will be submitted to the Research Ethics Committees of the Hospital Clinic and from Barcelona University (UB). Parents or guardians of the participants will sign an informed consent prior to the start. The study will be registered at clinicaltrials.gov. Although the recommended diet is based on the Mediterranean Diet and lifestyle intervention are safe, the investigators will be aware of any side effects in all visits to the participants. Regarding data confidentiality, Spanish Personal Data Protection Law (LOPD 15/99) compliance, all questionnaire data and biological samples pertaining to the participants will be anonymized and coded by a unique ID number. Data will be processed confidentially respecting the basic ethical principles of research that involves the usage of biological samples as established by Law 14/2007 on Biomedical Research and according to the Organic Law 15/1999 (concerning Data Protection), Law 41/2002 (concerning Patient Autonomy) and the Law 14/1986.
Recruitment and randomization:
The study will begin by contacting several schools in Barcelona to inform them about the trial. Each school's allocation group will be notified of its status by email. Then, the investigators will provide the schools with a recruitment flier to assess willingness to collaborate and grant us permission to contact interested families. Trained personnel will then contact the parents and explain the study details. Fieldworkers will review each candidate's eligibility criteria to ensure compliance with the study protocol. Participation in the study will be contingent upon obtaining informed consent from both the parents or guardians of the children and the teachers.
Implementation and adherence:
The healthy lifestyle intervention for all participants (intervention and control groups) This intervention had been developed and tried before as part of the SEÍSMO project by the Gasol Foundation. The SEÍSMO project is an intervention addressed to school-age children (6- to 12-year-old), their parents/caregivers, teaching, and non-teaching staff. It is part of a Multilevel Multicomponent intervention aimed to prevent overweight and obesity from early ages, and along all the developmental stages, until adulthood. The intervention includes 2 main modules: physical education module (PEM) and family module (FAM). The PEM includes a pedagogical guide that considers healthy eating, physical and sport, screen time, sleep duration, and phycological wellbeing in movement. The FAM, which is led by tutors, joins the PEM to increase the efficacy of the project because the family role is necessary to change habits. This includes family home activities, tutoring with the children, motivational messages, video tips about healthy habits for families and a healthy closing event. The family home activities combine with the PEM and each of them consists of a healthy habit promotion. The control group will be asked to refrain from eating nuts.
At the beginning of the intervention, all the educators from participant schools will receive a training to empower them toward healthy habits educational actions. After that, the modules of the SEÍSMO project will be deployed within children, families and the whole educative community.
The peanut intervention:
Families allocated in the intervention group will receive the whole skin roasted peanuts packed in daily doses (25 g per day, 750 g per month), starting the day that the investigators will visit the participants for the first time.
Adherence compliance:
Peanuts will be delivered every two months to keep in contact with the families and who will be asked to fill in a compliance form. To increase the success rate, the investigators will offer recipes with peanuts regularly and in different forms, mainly videos and infographics. the investigators will ask parents to supervise the intervention by checking the subject's adherence to peanuts consumption. Participants in the intervention group will be contacted in the middle of the study.
Data collection:
Trained professionals (nurses and nutritionists) will be in charge to collect participant characteristics at baseline and after 6 months (end of study), and will guide the adolescents through the questionnaires, perform measurements, and collect samples during school hours. Assessment of the characteristics will include a detailed assessment of health behaviors and health factors, including the following: anthropometry and body composition; diet; physical activity; emotion management; biochemical measurements. The assessment at the family and school environment levels will include surveys and questionnaires. Families and school principals will complete online questionnaires sent by e-mail or regular mail if necessary.
Assessment of the participant characteristics and outcomes:
- To evaluate the cognitive skills. Participants will be assessed at baseline and after the intervention using a battery of validated, standardized cognitive tests and behavioural rating scales, administered by trained neuropsychologists. Changes from baseline in the main score for each test will be used to evaluate neuropsychological outcomes - including working memory, selective attention, processing speed, inhibitory control, and fluid intelligence, as well as emotional well-being. A total of five validated instruments designed for the assessment of children and adolescents will be used: the Wechsler Intelligence Scale for Children Fifth Edition (WISC-V; selected subtests assessing working memory and processing speed), the d2-R Test of Attention (Revised Spanish adaptation), the Stroop Color-Word Test, Raven's Progressive Matrices (Raven-2), and the Children's Depression Inventory (CDI, Spanish adaptation).
- To evaluate the prebiotic and postbiotic effects, the investigators will collect capillary blood micro-samples, faeces and urine samples. By using these minimally invasive sampling methods, the investigators aim to minimise any discomfort for the participants to determine:
- Microbial phenolic metabolites in urine samples. A novel and validated targeted metabolomics method based on liquid chromatography coupled to high-resolution mass spectrometry will be used to identify and quantify microbial phenolic metabolites.
- Short-chain fatty acids in faecal samples. Their quantification will be performed using a headspace sampler connected to a gas chromatography-mass spectrometry system (HS-GC-MS) according to a previously described methodology.
- Gut microbiota characterization by 16s metagenomic analysis will be performed by experts from the Biomedical Research Institute of Malaga (IBIMA).
- To determine and evaluate the biomarkers of compliance. The concentration of very long change saturated fatty acids will be analyzed in capillary blood micro-samples by HS-GC-MS in the 30% of the volunteers at baseline and after 6 months of intervention as biomarkers of compliance. Adherence levels will be considered in the statistical analysis.
- To determine the circulating levels of vascular risk factor, satiety hormones and inflammation parameters.
The investigators will evaluate the levels of adiponectin, adipsin, C-peptide, ghrelin, GIP, GLP-1, glucagon, insulin, leptin, PAI-1, resistin, and visfatin, interleukin 6 (IL -6), interleukin-10 (IL-10), and monocyte chemotactic protein 1 (MCP-1) by ELISA - Multiplex immunoassays. Moreover, TXA2 and PGI2 will be analysed in urine samples.
- Conditions
- Cognitive Performance, Inflammation, Weight Change, Body, Adolescents
- Being tested
- Food (peanut)
- Keywords
- peanut, cognitive, inflammation, weight, adolescent, obesity, gut microbiota, healthy dietary, physical activity, sleeping, behaviour habits, Mediterranean diet
- Medical subject headings
- Inflammation, Body Weight Changes, Body Weight, Obesity, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Food (peanut)Other
After the recruitment, the participants will follow a peanut-free diet for two weeks.
| Study group | Role | What they receive |
|---|---|---|
| Peanuty group | Experimental | Families allocated in the intervention group will receive the whole skin roasted peanuts packed in daily doses (25 g per day, 750 g per month), starting the day that we will visit the participants for the first time. They will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months. Receives: Other: Food (peanut) |
| Control group | No intervention | Usual care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Changes in the depression score in healthy young adolescents after a daily intake of peanuts.
To measure depression score, the CDI Childhood Depression Inventory test will be used.
Measured: Baseline and after 6 months
Changes in the ability to concentrate, selective attention and processing speed in healthy young adolescents after a daily intake of peanuts.
To measure the ability to concentrate, selective attention and processing speed, the d2-R Attention Test (Revised) will be used.
Measured: Baseline and after 6 months
Changes in assessment of interference and cognitive control in healthy young adolescents after a daily intake of peanuts.
To measure the assessment of interference and cognitive control, the Stroop test will be used.
Measured: Baseline and after 6 months
Changes in processing speed, attention span and working memory in healthy young adolescents after a daily intake of peanuts.
To measure processing speed, attention span and working memory, the WISC-V Digits and Codes Subtest will be used.
Measured: Baseline and after 6 months
Changes in attention and inductive reasoning in healthy young adolescents after a daily intake of peanuts.
To measure in attention and inductive reasoning, the Raven-2 test will be used.
Measured: Baseline and after 6 months
Changes in Social cognition (emotion recognition and theory of mind) in healthy young adolescents after a daily intake of peanuts.
To measure Social cognition (emotion recognition and theory of mind), the NEPSY-II subtest will be used.
Measured: Baseline and after 6 months
Changes in pro- and anti-inflammatory biomarkers after a daily intake of peanuts in healthy young adolescents.
Cytokines (pg/mL), Monocyte chemoattractant protein-1 (MCP-1) (pg/mL), interleukin (IL)-6 and 10 (pg/mL), (mg/dL) will be assayed by immunoenzymatic methods.
Measured: Baseline and after 6 months
Changes in vascular biomarkers after a daily intake of peanuts in healthy young adolescents.
sVCAM-1 and sICAM-1 (ug/mL) will be assayed by immunoenzymatic methods.
Measured: Baseline and after 6 months
Changes in adiposity molecules after a daily intake of peanuts in healthy young adolescents
Adiponectin and adipsin (ug/mL), leptin (pg/mL), ghrelin (pg/mL), visfatin (pg/dL), resistin (pg/mL), insulin (pg/mL), glucagon (pg/dL), peptid C (pg/mL) and, PAI-1 (pg/mL) will be assayed by immunoenzymatic methods.
Measured: Baseline and after 6 months
Changes in body mass index after a daily intake of peanuts in healthy young adolescents
Body mass index (kg/m^2) are calculated after measure weight (kg) and height (meter).
Measured: Baseline, 3 and after 6 months
Secondary outcomes (13)
Changes in waist circumference after a daily intake of peanuts in healthy young adolescents
Change in waist circumference (cm) will be measured in triplicate
Measured: Baseline, 3 and after 6 months
Changes in blood pressure after a daily intake of peanuts in healthy young adolescents
Systolic and diastolic blood pressure (mmHg) will be measured using an automatic blood pressure monitor in triplicate.
Measured: Baseline, 3 and after 6 months
Changes in heart rate after a daily intake of peanuts in healthy young adolescents
Heart rate (bpm) is measured with an automatic monitor in triplicate.
Measured: Baseline, 3 and after 6 months
Changes in lipidic profile after a daily intake of peanuts in healthy young adolescents
Total cholesterol, HDL-cholesterol, LDL-cholesterol and triglycerides (mg/dL) will be measured using a portable Cardiocheck analyzer, through 40 µL of capillary and fasting blood.
Measured: Baseline and after 6 months
Changes in blood glucose after a daily intake of peanuts in healthy young adolescents
Fasting blood glucose (mg/dL) will be measured using a portable Cardiocheck analyzer
Measured: Baseline and after 6 months
Changes in nutrients and energy intake after regular peanut in healthy young adolescents
Dietary changes will be evaluated using a 151-item semi-quantitative food frequency questionnaire (Fernández-Ballart et al., 2010).
Measured: Baseline and after 6 months
Changes in physical activity after regular peanut in healthy young adolescents
To study the association between changes in physical activity and changes in adiposity parameters . Actigraph wGT3X-BT accelerometers that allow the registration of the amount and intensity of physical activity will be used during 7 days per evaluation time-point. To complete this information a diary with questions about the type of physical activity performed during the 7 days will be collected. A validated questionnaire will be also used to assess physical activity habits (Barbosa et al., 2007).
Measured: Baseline and after 6 months
Changes in sleep quality after regular peanut in healthy young adolescents
To study the association between changes in sleep quality and changes in adiposity parameters . Actigraph wGT3X-BT accelerometers that allow the registration of the amount and intensity of physical activity will be used during 7 days per evaluation time-point. To complete this information a diary with questions about the type of physical activity performed during the 7 days will be collected.
Measured: Baseline and after 6 months
Pubertal changes in healthy young adolescents after a daily intake of peanuts.
To measure pubertal changes, the Tanner's Pubertal scale self-assessment questionnaire will be used.
Measured: Baseline and after 6 months
Changes in the gut microbiota after a daily intake of peanuts in fecal samples of healthy young adolescents.
Fecal samples will be collected by the volunteers using a system for easy self-collection and stabilization of microbial DNA for gut microbiome profiling (OMNIgene - GUT). The genomic DNA will be extracted from fecal samples using the DNeasy PowerSoil Kit. Then, the 16s metagenomic analysis will be performed.
Measured: Baseline and after 6 months
Changes in the short-chain fatty acids after a daily intake of peanuts in biological samples of healthy young adolescents.
After acidifying the fecal samples with formic acid, a quantification of short-chain fatty acids will be performed using gas chromatography by direct injection according to previously described methodology (Zhao et al., 2006).
Measured: Baseline and after 6 months
Changes in the polyphenols and their metabolites after a daily intake of peanuts in biological samples of healthy young adolescents.
Identification and quantification of polyphenols will be determined using a high performance liquid chromatography-high resolution mass spectrometry (HPLC-HRMS) (Laveriano-Santos et al., 2022) and by ultra high-performance liquid chromatography coupled with triple quadrupole mass spectrometry (UHPLC-QqQ-MS/MS) (Martínez-Huélamo et al., 2015) methods.
Measured: Baseline and after 6 months
Changes in percentage of body fat in healthy young adolescents after a daily intake of peanuts.
Total adiposity are measured by bioelectrical impedance (body fat %, muscle mass %, visceral fat (kg), fat mass index (kg/m^2), lean mass index (kg/m^2)).
Measured: Baseline, 3 and after 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Nov 2023
- Study start29 Jan 2024
- Primary completion30 Jun 2025
- Study completion31 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cognitive PerformanceStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- A multi-school, two-arm parallel cluster-randomized controlled trial
- Masking
- None (open label)
- Enrolment
- 142 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Barcelona
- Sponsor type
- University, hospital or other
- Collaborators
- Gasol Foundation, Universitat Oberta de Catalunya, Institut d'Investigacions Biomèdiques August Pi i Sunyer
- Responsible party
- Principal investigator, Rosa M Lamuela-Raventós, University of Barcelona
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06127511
- Sponsor's protocol ID
- PEANUTY
- Acronym
- PEANUTY
- Status last verified
- Sep 2026
- First submitted
- 31 Oct 2023
- Last updated
- 4 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: The dataset analyzed during the current study is not publicly available due to national data regulations and for ethical reasons, e.g. we do not have the explicit written consent of the study volunteers to make their deidentified data available at the end of the study. However, data described in the manuscript, codebook, and analytic codes will be made available upon request by contacting the PI and Co-PI (peanuty2023@gmail.com). The request will be passed to all the members of the study for deliberation.
Study at a glance
From the registry record, last updated by the sponsor on 4 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Peanut Consumption on Cognitive Performance, Weight Management, and Inflammation in Young Adolescents
- ClinicalTrials.gov ID
- NCT06127511
- Acronym / sponsor ID
- PEANUTY / PEANUTY
- Conditions
- Cognitive Performance, Inflammation, Weight Change, Body, Adolescents
- Keywords
- peanut, cognitive, inflammation, weight, adolescent, obesity, gut microbiota, healthy dietary
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 142 participants (actual)
- Lead sponsor
- University of BarcelonaUniversity, hospital or other
- Collaborators
- Gasol Foundation, Universitat Oberta de Catalunya, Institut d'Investigacions Biomèdiques August Pi i Sunyer
- Study start
- 29 Jan 2024 (actual)
- Primary completion
- 30 Jun 2025 (actual)
- Study completion
- 31 Dec 2025 (actual)
- First posted
- 13 Nov 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Schools willing to participate will be randomly assigned to either the intervention or the control group. After the recruitment, the participants will follow a peanut-free diet for two weeks. Both arms will receive a multidimensional educational intervention designed by the Gasol Foundation to promote healthy dietary habits based on Mediterranean diet recommendations, along with exercise performance, healthy sleeping habits and emotional knowledge. Half of the participants (intervention group) will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months.
Detailed description
Background:
Regular nut consumption has been associated with reduced inflammation, oxidative damage, and improved vascular function, which may benefit cognitive function. Their content in phenolic acids, mainly p-coumaric and isoferulic acids may help prevent and cure diseases including Alzheimer's, diabetes, cancer, hypertension, and atherosclerosis that are associated with oxidative stress suggesting it could be used as a potential new neuroprotective tactic. Polyphenols have been shown to influence gut microbiota composition and activity, and their metabolites, including short-chain fatty acids (SCFAs), may modulate brain biochemistry by acting as neurotransmitters in the central nervous system, potentially leading to effects against depression and neurodegenerative disease.
Childhood is an important period for brain development, and nutrients aid the formation of new synaptic connections and support learning processes at school and in home environments. Adolescence is also a period where brain connectivity and complex behaviours are further refined. While a positive association has been observed between the consumption of healthy foods (fruits, vegetables, whole grains, fish, nuts, dietary fiber) and cognitive function, research on the association between nut consumption and cognitive health during adolescence is scarce.
In addition, evidence shows that incorporating peanut and peanut-based products into the diet does not lead to weight gain or higher body weight and may even promote long-term weight maintenance and increase linear growth due to their arginine content.
Due to the potential benefits of schools in preventing overweight and obesity, and the lack of research on the relationship between nut consumption and cognitive health during childhood and adolescence, the investigators plan to conduct an intervention study to investigate the association between peanut consumption and cognitive ability, weight management and inflammation in Spanish children aged 10-12 years. As the nutritional composition of peanuts can vary depending on their form, this study will examine the impact of the regular consumption of 25g of whole-skin roasted peanuts on cognitive function, mood, and school performance in healthy young adolescents.
Study design:
A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Schools willing to participate will be randomly assigned to either the intervention or the control group. After the recruitment, the participants will follow a peanut-free diet for two weeks. Both arms will receive a multidimensional educational intervention designed by the Gasol Foundation to promote healthy dietary habits based on Mediterranean diet recommendations, along with exercise performance, healthy sleeping habits and emotional knowledge. Half of the participants (intervention group) will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months.
Sample size:
Our study is designed based on previous research findings that suggest peanut consumption could influence cognitive performance and adiposity. Using a cluster design, the investigators aim to detect a significant difference of 1.3 (SD 0.8) absolute points in body mass per kJ consumed and a 6.9-unit (SD 3.1) improvement in cognitive performance score between the intervention and control groups, at a 95% confidence level, 80% power, and an estimated number of 20-40 students per school. With an intra-class correlation coefficient of 0.02, the investigators estimated a sample size of 6 schools (3 per arm) with a total of 200 participants (100 in each arm) at baseline, allowing for a 10% drop-out rate.
Ethical aspects:
The project will be submitted to the Research Ethics Committees of the Hospital Clinic and from Barcelona University (UB). Parents or guardians of the participants will sign an informed consent prior to the start. The study will be registered at clinicaltrials.gov. Although the recommended diet is based on the Mediterranean Diet and lifestyle intervention are safe, the investigators will be aware of any side effects in all visits to the participants. Regarding data confidentiality, Spanish Personal Data Protection Law (LOPD 15/99) compliance, all questionnaire data and biological samples pertaining to the participants will be anonymized and coded by a unique ID number. Data will be processed confidentially respecting the basic ethical principles of research that involves the usage of biological samples as established by Law 14/2007 on Biomedical Research and according to the Organic Law 15/1999 (concerning Data Protection), Law 41/2002 (concerning Patient Autonomy) and the Law 14/1986.
Recruitment and randomization:
The study will begin by contacting several schools in Barcelona to inform them about the trial. Each school's allocation group will be notified of its status by email. Then, the investigators will provide the schools with a recruitment flier to assess willingness to collaborate and grant us permission to contact interested families. Trained personnel will then contact the parents and explain the study details. Fieldworkers will review each candidate's eligibility criteria to ensure compliance with the study protocol. Participation in the study will be contingent upon obtaining informed consent from both the parents or guardians of the children and the teachers.
Implementation and adherence:
The healthy lifestyle intervention for all participants (intervention and control groups) This intervention had been developed and tried before as part of the SEÍSMO project by the Gasol Foundation. The SEÍSMO project is an intervention addressed to school-age children (6- to 12-year-old), their parents/caregivers, teaching, and non-teaching staff. It is part of a Multilevel Multicomponent intervention aimed to prevent overweight and obesity from early ages, and along all the developmental stages, until adulthood. The intervention includes 2 main modules: physical education module (PEM) and family module (FAM). The PEM includes a pedagogical guide that considers healthy eating, physical and sport, screen time, sleep duration, and phycological wellbeing in movement. The FAM, which is led by tutors, joins the PEM to increase the efficacy of the project because the family role is necessary to change habits. This includes family home activities, tutoring with the children, motivational messages, video tips about healthy habits for families and a healthy closing event. The family home activities combine with the PEM and each of them consists of a healthy habit promotion. The control group will be asked to refrain from eating nuts.
At the beginning of the intervention, all the educators from participant schools will receive a training to empower them toward healthy habits educational actions. After that, the modules of the SEÍSMO project will be deployed within children, families and the whole educative community.
The peanut intervention:
Families allocated in the intervention group will receive the whole skin roasted peanuts packed in daily doses (25 g per day, 750 g per month), starting the day that the investigators will visit the participants for the first time.
Adherence compliance:
Peanuts will be delivered every two months to keep in contact with the families and who will be asked to fill in a compliance form. To increase the success rate, the investigators will offer recipes with peanuts regularly and in different forms, mainly videos and infographics. the investigators will ask parents to supervise the intervention by checking the subject's adherence to peanuts consumption. Participants in the intervention group will be contacted in the middle of the study.
Data collection:
Trained professionals (nurses and nutritionists) will be in charge to collect participant characteristics at baseline and after 6 months (end of study), and will guide the adolescents through the questionnaires, perform measurements, and collect samples during school hours. Assessment of the characteristics will include a detailed assessment of health behaviors and health factors, including the following: anthropometry and body composition; diet; physical activity; emotion management; biochemical measurements. The assessment at the family and school environment levels will include surveys and questionnaires. Families and school principals will complete online questionnaires sent by e-mail or regular mail if necessary.
Assessment of the participant characteristics and outcomes:
- To evaluate the cognitive skills. Participants will be assessed at baseline and after the intervention using a battery of validated, standardized cognitive tests and behavioural rating scales, administered by trained neuropsychologists. Changes from baseline in the main score for each test will be used to evaluate neuropsychological outcomes - including working memory, selective attention, processing speed, inhibitory control, and fluid intelligence, as well as emotional well-being. A total of five validated instruments designed for the assessment of children and adolescents will be used: the Wechsler Intelligence Scale for Children Fifth Edition (WISC-V; selected subtests assessing working memory and processing speed), the d2-R Test of Attention (Revised Spanish adaptation), the Stroop Color-Word Test, Raven's Progressive Matrices (Raven-2), and the Children's Depression Inventory (CDI, Spanish adaptation).
- To evaluate the prebiotic and postbiotic effects, the investigators will collect capillary blood micro-samples, faeces and urine samples. By using these minimally invasive sampling methods, the investigators aim to minimise any discomfort for the participants to determine:
- Microbial phenolic metabolites in urine samples. A novel and validated targeted metabolomics method based on liquid chromatography coupled to high-resolution mass spectrometry will be used to identify and quantify microbial phenolic metabolites.
- Short-chain fatty acids in faecal samples. Their quantification will be performed using a headspace sampler connected to a gas chromatography-mass spectrometry system (HS-GC-MS) according to a previously described methodology.
- Gut microbiota characterization by 16s metagenomic analysis will be performed by experts from the Biomedical Research Institute of Malaga (IBIMA).
- To determine and evaluate the biomarkers of compliance. The concentration of very long change saturated fatty acids will be analyzed in capillary blood micro-samples by HS-GC-MS in the 30% of the volunteers at baseline and after 6 months of intervention as biomarkers of compliance. Adherence levels will be considered in the statistical analysis.
- To determine the circulating levels of vascular risk factor, satiety hormones and inflammation parameters.
The investigators will evaluate the levels of adiponectin, adipsin, C-peptide, ghrelin, GIP, GLP-1, glucagon, insulin, leptin, PAI-1, resistin, and visfatin, interleukin 6 (IL -6), interleukin-10 (IL-10), and monocyte chemotactic protein 1 (MCP-1) by ELISA - Multiplex immunoassays. Moreover, TXA2 and PGI2 will be analysed in urine samples.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- A multi-school, two-arm parallel cluster-randomized controlled trial
| Arm | Type | Receives |
|---|---|---|
| Peanuty group | Experimental | Other: Food (peanut)Families allocated in the intervention group will receive the whole skin roasted peanuts packed in daily doses (25 g per day, 750 g per month), starting the day that we will visit the participants for the first time. They will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months. |
| Control group | No intervention | –Usual care |
Who may qualify
- Ages
- 10 to 12 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- Eligible participants will be young adolescents, boys and girls, aged between 10 and 12 years who attend regular primary schools in Barcelona. The schools will assist with the participant recruitment through the classes and after that, a total of one-hundred students will be randomly included in each group. In all cases, participation will be voluntary and informed consent will be obtained prior to the study.
Key exclusion criteria (1 listed)
- The exclusion criteria will be history of allergy or intolerance to peanuts, any medical conditions or dietary restrictions that would affect peanut consumption, being able to understand Spanish or Catalan, and use of antibiotics in the month prior to the study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Food (peanut)After the recruitment, the participants will follow a peanut-free diet for two weeks. | Other | Peanuty group |
Primary outcome
Changes in the depression score in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline and after 6 months
To measure depression score, the CDI Childhood Depression Inventory test will be used.
Changes in the ability to concentrate, selective attention and processing speed in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline and after 6 months
To measure the ability to concentrate, selective attention and processing speed, the d2-R Attention Test (Revised) will be used.
Changes in assessment of interference and cognitive control in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline and after 6 months
To measure the assessment of interference and cognitive control, the Stroop test will be used.
Changes in processing speed, attention span and working memory in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline and after 6 months
To measure processing speed, attention span and working memory, the WISC-V Digits and Codes Subtest will be used.
Changes in attention and inductive reasoning in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline and after 6 months
To measure in attention and inductive reasoning, the Raven-2 test will be used.
Changes in Social cognition (emotion recognition and theory of mind) in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline and after 6 months
To measure Social cognition (emotion recognition and theory of mind), the NEPSY-II subtest will be used.
Changes in pro- and anti-inflammatory biomarkers after a daily intake of peanuts in healthy young adolescents.
Time frame: Baseline and after 6 months
Cytokines (pg/mL), Monocyte chemoattractant protein-1 (MCP-1) (pg/mL), interleukin (IL)-6 and 10 (pg/mL), (mg/dL) will be assayed by immunoenzymatic methods.
Changes in vascular biomarkers after a daily intake of peanuts in healthy young adolescents.
Time frame: Baseline and after 6 months
sVCAM-1 and sICAM-1 (ug/mL) will be assayed by immunoenzymatic methods.
Changes in adiposity molecules after a daily intake of peanuts in healthy young adolescents
Time frame: Baseline and after 6 months
Adiponectin and adipsin (ug/mL), leptin (pg/mL), ghrelin (pg/mL), visfatin (pg/dL), resistin (pg/mL), insulin (pg/mL), glucagon (pg/dL), peptid C (pg/mL) and, PAI-1 (pg/mL) will be assayed by immunoenzymatic methods.
Changes in body mass index after a daily intake of peanuts in healthy young adolescents
Time frame: Baseline, 3 and after 6 months
Body mass index (kg/m^2) are calculated after measure weight (kg) and height (meter).
13 secondary outcomes
Changes in waist circumference after a daily intake of peanuts in healthy young adolescents
Time frame: Baseline, 3 and after 6 months
Changes in blood pressure after a daily intake of peanuts in healthy young adolescents
Time frame: Baseline, 3 and after 6 months
Changes in heart rate after a daily intake of peanuts in healthy young adolescents
Time frame: Baseline, 3 and after 6 months
Changes in lipidic profile after a daily intake of peanuts in healthy young adolescents
Time frame: Baseline and after 6 months
Changes in blood glucose after a daily intake of peanuts in healthy young adolescents
Time frame: Baseline and after 6 months
Changes in nutrients and energy intake after regular peanut in healthy young adolescents
Time frame: Baseline and after 6 months
Changes in physical activity after regular peanut in healthy young adolescents
Time frame: Baseline and after 6 months
Changes in sleep quality after regular peanut in healthy young adolescents
Time frame: Baseline and after 6 months
Pubertal changes in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline and after 6 months
Changes in the gut microbiota after a daily intake of peanuts in fecal samples of healthy young adolescents.
Time frame: Baseline and after 6 months
Changes in the short-chain fatty acids after a daily intake of peanuts in biological samples of healthy young adolescents.
Time frame: Baseline and after 6 months
Changes in the polyphenols and their metabolites after a daily intake of peanuts in biological samples of healthy young adolescents.
Time frame: Baseline and after 6 months
Changes in percentage of body fat in healthy young adolescents after a daily intake of peanuts.
Time frame: Baseline, 3 and after 6 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Sep 2026.
- Individual participant dataSharing planned: No. The dataset analyzed during the current study is not publicly available due to national data regulations and for ethical reasons, e.g. we do not have the explicit written consent of the study volunteers to make their deidentified data available at the end of the study. However, data described in the manuscript, codebook, and analytic codes will be made available upon request by contacting the PI and Co-PI (peanuty2023@gmail.com). The request will be passed to all the members of the study for deliberation.
Related trials for Cognitive Performance
Not yet recruiting
Effects of Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) on Cognition, Dual-Task Performance, and Interoceptive Accuracy
Cognition, Healthy Volunteers
Not yet recruiting
Effects of Cognitive Restructuring Intervention on Competitive State Anxiety and Volleyball Skill Performance Among Female Collegiate Volleyball Players in Guangzhou, China
Competitive State Anxiety, Volleyball Skill Performance
Not yet recruitingObservational study
EEG Markers From Polysomnography and Cognitive Performance in Obstructive Sleep Apnea
Obstructive Sleep Apnea, Cognitive Impairment
Not yet recruiting
Dual-Task Core Stabilization Training in Chronic Nonspecific Low Back Pain
Chronic Nonspecific Low Back Pain
Recruiting
A Clinical Trial to Evaluate the Effects of Adrenal Adapt on Sleep Quality, Daytime Energy, Stress Resilience, and Cognitive Performance.
Improves Daytime Energy Levels, Reduces Afternoon Energy Crashes and Midday Fatigue
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Food (peanut) in people with Cognitive Performance and Inflammation, run by University of Barcelona at 1 site in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Changes in the depression score in healthy young adolescents after a daily intake of peanuts. (time frame: Baseline and after 6 months). The study lists 10 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Sep 2026.