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Completed

NCT Number: NCT02251379

Environmental Control as Add-on Therapy in Childhood Asthma

This study evaluates the effects of adding on an environmental home intervention to standard asthma medication management on controller medication requirements among children and adolescents with asthma. The investigators hypothesize that the addition of an individually-tailored, multi-faceted Environmental Control Strategy (ECS) to guidelines-based controller medication will result in less controller medication requirement and allergic inflammation than controller medication alone among urban asthmatic children.

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Key information

Age range

5 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Johns Hopkins University

Baltimore, Maryland, 21287, United States

About this study

The study is a parallel arm study of an individually tailored, multi-faceted ECS plus controller medication titration versus controller medication titration alone. After a 4-week run-in period to stabilize the asthma, the investigators will randomize 200 Baltimore children with persistent asthma and a recent exacerbation in a 1:1 ratio to the two arms and follow the children for six months. There will be five clinic visits and three home visits over this time period for clinical and home assessments, respectively. There will be up to four environmental intervention visits for participants randomized to the environmental control plus controller medication group. The environmental modules include mouse, cockroach, furry pets, dust mites, and smoking. Air purifiers and laundered bedding are also included in this arm. Participants randomized to the controller medication group have the option of having one home visit after completing the study at which the participants will receive home intervention services that the environmental control plus controller medication group received. Participants will have repeated assessment of: controller medication requirements; secondary clinical, physiologic, and inflammatory outcomes; and particulate matter (PM), air nicotine, and allergen levels.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have physician-diagnosed asthma at least 1 year prior to the baseline visit, or asthma symptoms for at least 1 year
  • Meet criteria for current persistent asthma defined as either:
  • On a long-term controller medication for asthma, or
  • Meet National Asthma Education and Prevention Program (NAEPP) guideline requirements for persistent disease:(46)
  • Asthma symptoms 3 or more days per week over the past 2 weeks or
  • Nocturnal asthma symptoms at least 3 times in the past month
  • Have evidence of uncontrolled disease as defined by at least one of the following:
  • One asthma-related unscheduled visit to an emergency department (ED), clinic or urgent care facility in the previous 12 mo
  • One asthma-related overnight hospitalization in the previous 12 mo
  • One or more bursts of oral corticosteroids in the previous 12 mo
  • Reside within a geographic area of the study site so that home visits are feasible.
  • Have no plans to move within the upcoming 6 months
  • Have insurance to cover prescription medications.
  • Have a positive skin test (net wheal ≥2mm) to cat, dog, mouse, cockroach, or dust mites or have a positive cat, dog, mouse, German cockroach, or D. farinae-specific immunoglobulin E (IgE) test, as quantified using the ImmunoCAP system (≥0.35 kU/L)

Exclusion criteria

  • Lung disease, other than asthma, that requires daily medication
  • Cardiovascular disease that requires daily medication, excluding hypertension
  • Taking a beta-blocker
  • Allergy to dairy
  • On Xolair < 5 months
  • On immunotherapy and has not reached maintenance dose
  • Sleeping in another home 4 or more nights/week
  • Active smoker defined as a positive urine screen for high levels of urine cotinine
  • Unable to access areas of home necessary to conduct extermination

Treatment and study plan

Flovent Diskus

Drug

Inhaled corticosteroids

Other names: Flovent Diskus, 50 mcg, 100mcg, 250 mcg

Home Environmental Intervention

Other

Mouse, Cockroach, Furry pets, Dust mites, Smoking, air purifiers, laundered bedding

ADVAIR DISKUS

Drug

inhaled corticosteroids + long-acting beta agonist

Primary outcomes

  1. The Medication Treatment Step Assigned

    Time frame: 6 month clinic visit

    The controller medication treatment step that was assigned at the visit, which is based on the current controller medication treatment step and the current level of asthma control. The range is from 0-6, with 0 indicating no controller medication and 6 indicating high dose inhaled corticosteroids plus long-acting beta agonist.

Secondary outcomes

  1. Daily Inhaled Corticosteroid Dose

    Time frame: 6 months

    micrograms of inhaled corticosteroids (daily)

  2. Exhaled Nitric Oxide

    Time frame: 6 months

    Exhaled nitric oxide in parts per billion.

  3. Number of Asthma Symptom Days

    Time frame: 6 months

    Number of asthma symptom days in the past two weeks will be a measure of asthma control.

  4. Number of Asthma Exacerbations

    Time frame: 6 months

    Asthma exacerbations will be assessed by number of acute visits to the emergency department (ED), hospitalizations and urgent doctor visits.

  5. FEV1/FVC

    Time frame: 6 months

    Forced expiratory volume at one second/forced vital capacity (FEV1/FVC) will be evaluated as a continuous variable. This is a ratio without any units.

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Registry information

Acronym: ECATCh

Important dates

Study start
2014
Primary completion
2018
Study completion
2018
First posted
Sep 29, 2014
Registry last updated
Nov 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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