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Barrier Enhancement for Eczema Prevention

A Randomised Controlled Trial to Determine Whether Application of Emollient From Birth Can Prevent Eczema in High Risk Children.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04680520
Acronym
BEEP
Enrollment
1394
Registered
2020-12-23
Start date
2014-11-01
Completion date
2022-01-01
Last updated
2022-11-28

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

Conditions

Eczema

Brief summary

The primary objective is to determine whether advising parents to apply emollient (moisturiser) to their child's skin for the first year of life in addition to best practice infant skin care advice can prevent or delay the onset of eczema in high-risk children, when compared with a control group who are given the best practice infant skin care advice only.

Interventions

OTHERExperimental (Doublebase Gel® or Diprobase Cream®)

Emollient (Doublebase Gel® or Diprobase Cream®) use on the skin. The emollient should be applied at least once a day.

OTHERBest practice skin care advice booklet

This is a booklet containing advice on best practice skin care. This will contain information on avoiding soap etc.

Sponsors

National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
University of Nottingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
No minimum to 21 Days
Healthy volunteers
Yes

Inclusion criteria

* child has a first degree relative with parental reported doctor diagnosis of eczema, allergic rhinitis or asthma * child up to 21 days old * consenting adult has the ability to understand English

Exclusion criteria

* preterm birth (defined as birth prior to 37 weeks gestation) * sibling (including twin) previously randomized to this trial. If multiple births, the first child will be randomized into the trial. * child has a severe widespread skin condition that would make the detection and/or assessment or eczema difficult * child has a serious health issue, which, at parent or investigator discretion, would make it difficult for the family to take part in the trial * any condition that would make the use of emollient inadvisable or not possible

Design outcomes

Primary

MeasureTime frameDescription
A diagnosis of eczema between 12 and 24 months of age (defined as meeting the United Kingdom (UK) Working Party Diagnostic Criteria for Atopic Dermatitis).24 monthsTo reflect the chronicity of eczema, these criteria refer to signs and symptoms present over the past year. Applying the criteria at 24 months of age will therefore detect eczema present only between the ages of 12 and 24 months, thus excluding transient eczematous rashes which are common in the first year of life and often reported by parents as eczema but less likely to be true atopic eczema

Secondary

MeasureTime frameDescription
Presence of visible eczema at 24 months (skin examination by researcher).24 monthsPresence of visible eczema at 24 months (skin examination by researcher).
Time to onset of eczema24 monthsFirst parental report of a clinical diagnosis of eczema. First topical corticosteroid and /or immunosuppressant prescription for eczema.
Presence of other allergic diseases using parental reports, allergic sensitization and confirmed diagnosisUpto 24 monthsParental reported wheezing and allergic rhinitis between 12 and 24 months. Parental report of a clinical diagnosis of food allergy at 12 and 24 months. Parental report of food allergy at 12 and 24 months. Parents will be specifically questioned about cow's milk, egg, peanuts, and other nuts plus any other food. Allergic sensitisation at 24 months to any of the following common allergens: milk, egg, peanut, cat, grass pollen, house dust mite. Confirmed diagnosis of food allergy at 24 months to milk, egg, peanut or 'any of milk, egg or peanut'. The diagnosis is derived from a combination of parental report, allergic sensitisation and food challenge.
Child health-related quality adjusted life years.Upto 24 monthsChild health utility 9 dimension (CHU-9D) at 24 months in order to estimate quality adjusted life years (QALYs).
Presence of parental report of eczema between birth and 24 months.Up to 24 monthsAssessed using: Any parental report of a clinical diagnosis of eczema. Completion by parents of UK Working Party Diagnostic Criteria for Atopic Dermatitis at 12 and 24 months.
Cost or treatments- health economic outcomesUp to 24 monthsHealth care resource use at 3, 6, 12, 18 and 24 months. Cost effectiveness and cost-utility at 24 months (combining health resource use and health-related quality of life outcomes).
Severity of eczema with EASI eczema severity scalesUp to 24 monthsAssessed using eczema area and severity index (EASI) at 24 months. The area score is recorded for each of four regions of the body: head and neck, trunk, upper limbs and lower limbs. The area score is the percentage of skin affected by eczema for each body region. The scores given are from 0-6 where a score of 0 is given when the percentage of skin affected by eczema in the region is 0%, and a score of 6 is given when 90-100% of the region is affected by eczema. The severity score is recorded for each of the four body regions for four signs: redness, thickness, scratching and lichenification. Scores are given from 0-3 where a score of 3 is for most severe signs.
Severity of eczema with POEM eczema severity scalesUp to 24 monthsAssessed using patient oriented eczema measure (POEM) at 12 and 24 months. The scores given are from 0-28, where a score of 28 is for the most severe.
Parental health-related quality adjusted life years.Upto 24 monthsParental quality of life measured using the EQ-5D-5L at baseline and 24 months in order to estimate change in parental QALYs, if any.

Other

MeasureTime frameDescription
Parental quality of life measured using EQ-5D-5L at 36, 48 and 60 months in order to estimate parental QALYs36, 48 and 60 monthsParental quality of life measured using EQ-5D-5L at 36, 48 and 60 months in order to estimate parental quality adjusted life years (QALYs)
Health care resource use at 36, 48 and 60 months36, 48 and 60 monthsHealth care resource use at 36, 48 and 60 months
Presence of eczema in the previous year at 36, 48 and 60 months based on parental report of a clinical diagnosis of eczema36, 48 and 60 monthsPresence of eczema in the previous year at 36, 48 and 60 months based on parental report of a clinical diagnosis of eczema
Parental report of clinical diagnosis of eczema from the age of 12 months to 60 months12 months to 60 monthsParental report of clinical diagnosis of eczema from the age of 12 months to 60 months
Parental report of clinical diagnosis of food allergy by 60 monthsBy 60 monthsParental report of clinical diagnosis of food allergy by 60 months
Cost utility and cost-effectiveness at 60 months (combining health resource use and health-related quality of life outcomes)60 monthsCost utility and cost-effectiveness at 60 months (combining health resource use and health-related quality of life outcomes)
Any parental report that in their opinion their child has eczema at 3, 6, 12, 24, 36, 48 and 60 months3, 6, 12, 24, 36, 48 and 60 monthsAny parental report that in their opinion their child has eczema at 3, 6, 12, 24, 36, 48 and 60 months
Presence of eczema at 36, 48 and 60 months based on completion by parents of UK Working Party Diagnostic Criteria for Atopic Dermatitis36, 48 and 60 monthsPresence of eczema at 36, 48 and 60 months based on completion by parents of UK Working Party Diagnostic Criteria for Atopic Dermatitis
Severity of eczema at 36, 48, and 60 months as measured by POEM36, 48, and 60 monthsSeverity of eczema at 36, 48, and 60 months as measured by Patient Oriented Eczema Measure (POEM)
Parental reported wheezing, at 36, 48 and 60 months36, 48 and 60 monthsParental reported wheezing, at 36, 48 and 60 months
Parental reported allergic rhinitis at 36, 48 and 60 months36, 48 and 60 monthsParental reported allergic rhinitis at 36, 48 and 60 months
Parental reported food allergy symptoms at 36, 48 and 60 months36, 48 and 60 monthsParental reported food allergy symptoms at 36, 48 and 60 months
Parental report of a clinical diagnosis of asthma or allergic rhinitis by 60 monthsBy 60 monthsParental report of a clinical diagnosis of asthma or allergic rhinitis by 60 months
Parental report of a clinical diagnosis of food allergy at 36, 48 and 60 months36, 48 and 60 monthsParental report of a clinical diagnosis of food allergy at 36, 48 and 60 months
CHU-9D at 36, 48 and 60 months in order to estimate QALYs36, 48 and 60 monthsChild health utility 9 dimension (CHU-9D) at 36, 48 and 60 months in order to estimate quality adjusted life years (QALYs)

Countries

United Kingdom

Outcome results

None listed

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