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临床试验/NCT03409367
NCT03409367已完成不适用

A Community-based Assessment of Skin Care, Allergies, and Eczema

Oregon Health and Science University8 个研究点 分布在 1 个国家目标入组 1,260 人开始时间: 2018年7月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,260
试验地点
8
主要终点
Provider-diagnosed Atopic Dermatitis

研究概览

简要总结

Atopic dermatitis (AD) affects over 9 million children in the U.S. and often heralds the development of asthma, food allergy, skin infections and neurodevelopmental disorders. Recent advances identify skin barrier dysfunction to be the key initiator of AD and possibly allergic sensitization.

Our central hypothesis is that daily emollient use from birth can prevent the development of AD in a community setting and into newborns unselected for risk. The results of a community-based clinical trial utilizing a pragmatic trial design will be immediately applicable to the population at large and will establish a new standard of care for all newborns.

详细描述

AD affects over 9 million children in the U.S. and ranks first among all skin conditions in global disability burden. AD often heralds the development of several comorbidities including asthma, food allergy, skin infections and neurodevelopmental disorders. Because of the significant socioeconomic impact of atopic dermatitis and its effect on the quality of life of children and families, there have been decades of research focused on prevention with limited success. Recent advances in cutaneous biology identify epidermal defects and skin barrier dysfunction to be the key initiators of atopic dermatitis and possibly allergic sensitization. Our central hypothesis is that emollient therapy from birth can prevent the development of AD. The findings of this trial will support the development of evidence-based skin care clinical guidelines for infants that currently do not exist. Recently, our international multi-centered clinical trial found enhancing early skin barrier function with daily emollient use from birth significantly reduces the risk of AD development in high-risk populations by 50%. With CASCADE, we extend this work into the community setting and into newborns unselected for risk, so results will be immediately applicable to the population at large and will establish a new standard of care for all newborns.

The specific aims are as follows:

  1. Perform a community-based pragmatic randomized controlled trial investigating whether daily full-body emollient application starting in the first 2 months of life prevents atopic dermatitis in a real-world setting. The population for this trial consists of newborns between 0-2monthsof age, not selected for risk. Recruitment of families will occur during the course of routine care within primary care offices that are members of practice-based research networks(PBRNs).The intervention includes general skin care recommendations plus full-body daily lipid-rich emollient use. The control population will receive general skin care advice only and refrain from daily emollient use. The primary outcome will be the cumulative incidence of atopic dermatitis at age 24 months as determined by blinded clinicians trained in the diagnosis of AD. Key secondary clinical outcomes include time to disease onset and incidence of self-reported food allergy and wheeze using parental questionnaires.
  2. As an exploratory aim, determine whether a family history of allergic disease and key early life exposures such as pet ownership modify the preventive effect of emollient therapy on atopic dermatitis. While the primary objective of this clinical trial is to determine the effectiveness of an emollient intervention in a real-world setting, data will be gathered on allergy history in the family and pet ownership-variables that may modify the effect of emollient therapy. Future implementation studies may target subpopulations found most likely to benefit from emollient intervention.

Twenty-five primary care clinics that participate in PBRNs from Oregon, Colorado, Wisconsin and North Carolina are the setting for the study protocol. The expected results from this project would represent a major public health breakthrough with the potential for reducing the atopic disease burden on a global scale.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Prevention
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

盲法说明

Due to the nature of the intervention, it is not possible blind dyads to the intervention. Administering a placebo emollient is impossible as there are no active ingredients in the emollient and using an emollient that has no barrier improvement properties may irritate the skin. The clinician completing the final assessment will be a blinded assessor.

Clinic staff will not be informed of participant enrollment or study arm. Parents will be instructed not to disclose their treatment group to clinic staff. Clinicians and clinic staff will direct participants to follow skin care recommendations as described by the study materials.

Blinded researchers will be responsible for health record review to collect the primary outcome. At completion of health record review, researchers will complete a form measuring whether the assessor became unblinded while reviewing the record.

入排标准

年龄范围
1 Day 至 63 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Parent can provide electronic signed and dated informed consent form.
  • Parent is willing and able to comply with all study procedures for the duration of the study.
  • Parent is a primary caretaker of an infant 0 to 2 months of age.
  • Parent is 18 years of age or older at time of consent.
  • Parent can speak, read, and write in English or Spanish.
  • Parent has a valid e-mail address or phone that can receive text messages
  • Parent has reliable access to the internet.
  • Infant is a patient of a participating Meta-LARC clinic site at the time of consent.

排除标准

  • Infant was born at less than 25 weeks gestational age.
  • Infant has established eczema as diagnosed by the primary healthcare provider at clinic site of enrollment per parent report.
  • Infant has known adverse reaction to petrolatum-based emollients.
  • Infant has an immunodeficiency genetic syndrome such as Wiskott-Aldrich Syndrome or Severe Combined Immunodeficiency Syndrome.
  • Infant has extremely low birth weight (less than 1000g or 2.2 lbs at birth).
  • Infant has a sibling enrolled in the study.
  • Parent is unwilling or unable to comply with study procedures.

结局指标

主要结局

Provider-diagnosed Atopic Dermatitis

时间窗: up to 24 months

The cumulative incidence of AD as recorded in health records. Trained clinicians will assess for AD at each clinic visit and record in the health record.

次要结局

  • Atopic Dermatitis With or Without Prescription or Over-the-counter Therapies in Chart (Ordinal)(Up to 24 months)
  • Prescribed or Over-the-counter Topical Skin Medication by Parent Report(up to 24 months)
  • Skin Infections Diagnosed and Recorded in Chart Review(up to 24 months)
  • Provider-diagnosed Asthma(up to 24 months)
  • Parent Report of Atopic Dermatitis(up to 24 months)
  • Severity of AD Symptoms Using POEM(24 months of age)
  • Severity of AD Symptoms Using IDQoL(24 months)
  • Food Allergy Symptoms(12 months, 24 months or both)
  • Food Allergy Diagnosis With Positive Test(up to 24 months)
  • Atopic Dermatitis by UK Working Party Criteria(up to 24 months)
  • Atopic Dermatitis With Prescription or Over-the-counter Therapies in Chart(up to 24 months)
  • Atopic Dermatitis by Children's Eczema Questionnaire(up to 24 months)
  • Primary Outcome of Provider-diagnosed Atopic Dermatitis(up to 12 months)
  • Provider-diagnosed Atopic Dermatitis at 18 Months(up to 18 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Eric Simpson

Professor

Oregon Health and Science University

研究点 (8)

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