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The TreEat Study- Can Early Introduction of Tree Nuts Prevent Tree Nut Allergy in Infants With Peanut Allergy

Can Early Introduction of Tree Nuts Prevent Tree Nut Allergy in Infants at High Risk of Tree Nut Allergy: The TreEat Study: a Randomised, Open-label Controlled Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04801823
Acronym
TreEat
Enrollment
212
Registered
2021-03-17
Start date
2021-06-01
Completion date
2025-06-29
Last updated
2026-02-19

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

Conditions

Food Allergy in Infants, Nut Allergy

Keywords

food allergy, nut allergy

Brief summary

Early and regular ingestion of the common allergens, peanut and egg has been shown to be an effective allergy prevention strategy. It is not clear whether this is also true of tree nut allergy. Current practice in many Australian allergy clinics for children with peanut allergy (high risk of tree nut allergy), is to advise families to introduce each individual tree nut into their child's diet via a cautious home introduction protocol without prior allergy testing (screening). The safety and effectiveness of an early and regular ingestion strategy for the prevention of tree nut allergy has not been formally evaluated and it is known that around a third of children with peanut allergy develop one or more other nut allergies. This trial is a 2-armed, open-label, randomized, controlled trial (RCT) to assess the safety and efficacy of a supervised hospital based multi-tree nut (almond, cashew, hazelnut and walnut) oral food challenge (OFC) + then home introduction of the remaining tree nuts versus standard care (home introduction of all 8 tree nuts) in infants with peanut allergy to reduce the risk of developing tree nut allergy.

Interventions

Cautious, graded introduction of individual tree nuts

OTHERMulti Nut oral food challenge

In hospital multi nut oral food challenge (almond, cashew, hazelnut, walnut)

Sponsors

Murdoch Childrens Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
4 Months to 11 Months
Healthy volunteers
No

Inclusion criteria

Infants aged greater than 4 months and less than 11 months of age diagnosed with IgE-mediated peanut allergy in conjunction with a positive SPT (≥3mm) or sIgE (specific immunoglobulin E) (\>0.35 kU/L)

Exclusion criteria

* Any history of severe food induced anaphylaxis. Defined as reaction requiring 2 doses of intramuscular (IM) adrenaline. * Pre-existing tree nut allergy (parent-reported). * Any tree nut already tolerated (ingestion on \>3 occasions without reaction of around 1 teaspoon) * SPT or sIgE performed to any tree nuts * Not commenced or unable to eat solid food * Prescribed beta-blocker medication

Design outcomes

Primary

MeasureTime frameDescription
Difference between the two treatment arms in the proportion of participants with clinical confirmed tree nut allergy at 18 months of age18 months of ageTree nut allergy outcomes at 18 months will be defined as: 1. Allergic - has evidence of tree nut sensitization (SPT\>=3mm) and has had a reaction consistent with IgE (immunoglobulin E) mediated food allergy OR positive formal OFC 2. Tree nut tolerant- successfully tolerated the tree nut at home on more than 3 occasions of at least 1 teaspoon of nut per occasion OR has had a negative formal OFC. 3. Inconclusive -has an unknown outcome as ingestion has not occurred and participant declines OFC.

Secondary

MeasureTime frameDescription
Difference between the two treatment arms in the proportion of participants with ongoing peanut allergy at 18 months of age18 months of agePeanut allergy will be defined as peanut sensitization (SPT \>=3mm) AND has had a reaction consistent with IgE mediated food allergy since randomization OR positive formal OFC
Difference between the two treatment arms in the proportion and severity of reported adverse events (AE) related to tree nut ingestion.18 months of ageNumber and severity of adverse events (AE) as assessed by standardised predetermined criteria, related to tree nut ingestion from randomization to 18 months of age collected via parent questionnaire and medical history.
Difference between the two treatment arms in the proportion and severity of solicited AEs related to tree nut ingestion.18 months of ageNumber and severity of solicited AEs as assessed by standardized predetermined criteria, related to tree nut ingestion from randomization to 18 months of age collected via parent questionnaire and medical history.
Difference between the 2 treatment arms in the number of tree nuts ingested.18 months of ageParent reported tree nut ingestion history based on questionnaire at baseline and 18 months of age. 0-8 tree nuts and the higher the number of tree nuts the better.
Difference between the 2 treatment arms in the frequency of tree nuts ingested.18 months of ageParent reported tree nut ingestion history based on questionnaire at baseline and 18 months of age. Range will be never to daily with higher frequency better.
Difference between the two treatment arms in mean change from baseline of Quality of Life Scores using the Food Allergy Quality of Life Questionnaire (FAQLQ-PF)- Parent Form at 18 months of age.Baseline and 18 months of ageThe Food Allergy Quality of Life Questionnaires (FAQLQ) are disease-specific health-related quality of life (HRQL) questionnaires for patients with food allergy. FAQLQ-PF (Parent Form), completed by parents of children aged 0-12 years consists of 30 items over 3 domains (emotional impact, food anxiety, social and dietary restrictions). Total and domain scores are calculated by dividing the sum of completed items by the number of completed items. Questions are based on a 6 point Likert scale with higher scores indicating greater impact on quality of life
Difference between the two treatment arms in the mean change from baseline in State/Trait anxiety scores using the State/Trait Anxiety InventoryBaseline and 18 months of ageThe State-Trait Anxiety Inventory (STAI) is a psychological inventory based on a 4-point Likert scale and consists of 40 questions on a self-report basis. The STAI measures two types of anxiety - state anxiety, or anxiety about an event, and trait anxiety, or anxiety level as a personal characteristic. The total score ranges from 0-63 with higher scores positively correlated with higher levels of anxiety.
Difference in the number of allergy-related healthcare visits from randomization to 18 months of age between the treatment arms18 months of ageCaptured per number of hospitalizations, Emergency room (ER) visits, physician office visits, and medications / number of prescriptions from randomization to 18 months of age.

Countries

Australia

Contacts

PRINCIPAL_INVESTIGATORKirsten Perrett, MD. PhD

Murdoch Childrens Research Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026