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AsthmaVent - Effect of Mechanical Ventilation on Asthma Control in Children (AsthmaVent)

2016년 5월 11일 업데이트: University of Aarhus

AsthmaVent is a multi-center study, investigating the association between indoor air quality and childhood asthma.

In Denmark, we spend more and more time indoors. Our houses are built airtight to save energy and are difficult to ventilate. We are thus more exposed to our indoor air than ever before. We know that indoor air contains many different components that can affect our airways inappropriately and particularly children with asthma, who have sensitive airways are sensitive to these components. The AsthmaVent project examines whether increased ventilation is able to improve the indoor environment to such an extent that the asthma disease control, for children with asthma and house dust mite allergy improves, resulting in need for less medication.

Previous studies have pointed towards a beneficial effect of mechanical ventilation, on both the indoor air quality and on children's health and quality of life. There is not currently a consensus in this area, as studies so far have not been large or good enough to confidently determine the effect.

This project is big and is designed so that it takes into account the sources of error seen in previous studies on the topic.

We include, over a 3-year period (2012-2014), a total of 80 children with asthma and house dust mite allergy aged 6-18 years, from pediatric departments in Aarhus, Odense, Kolding, Randers and Herning. They are divided into two groups, receiving either active ventilation or placebo ventilation, meaning a non-functioning ventilation system that just recirculates the air in the room. Ventilation systems are installed in the fall and winter and ventilate the child's bedroom during 9 months. Indoor air quality and asthma control are assessed every 3 months, both at home visits were air quality and allergen levels of house dust mites are studies and at visits to the outpatient clinics with control of asthma parameters and quality of life.

The project involves collaboration between several institutions with an interest in indoor air quality in relation to allergies and asthma and with great expertise in the field.The project was initiated by CISBO (Centre for Indoor Environment and Health in Dwellings), a center consisting of several institutions in Denmark dealing with indoor environment: Department of Public Health at Aarhus University and University of Copenhagen, Danish Building Research Institute and the Technical University of Denmark.

Since asthma is the most common chronic childhood disease in Denmark and since the development of allergies and asthma has high social and personal costs, it is important for both society and the individual family, to find out whether simply improving the indoor air quality by increased ventilation can lead to an improvement in asthma disease control.

연구 개요

상세 설명

The aim of the project is to investigate whether increased ventilation is able to improve the indoor air quality and thereby asthma disease control for children with asthma and house dust mite allergy.

Hypotheses:

  1. An increased ventilation in the home will reduce the need for inhaled steroids in children with house dust mite allergy and asthma.
  2. An increased ventilation in the home will improve the quality of life in children with house dust mite allergy and asthma.
  3. An increased ventilation in the home will improve the indoor environment and thus improve asthma disease control in children with house dust mite allergy and asthma.

Materials and methods: The study is a randomized double-blind placebo-controlled intervention study. The intervention is balanced mechanical ventilation in the bedroom of children with asthma and house dust mite allergy during 9-months.

Population: Over 3 year period (2012-2014) 80 families with asthmatic children aged 6-18 years will be included from out-patient clinics at the children's department of the University Hospitals of Aarhus and Odense and regional hospitals in Kolding, Randers and Herning. Families will also be included from private pediatric clinics in Aarhus.

Randomization: After inclusion children are randomized to either active ventilation or placebo ventilation. Randomization is done in blocks of 4 by center.

Intervention: The ventilation units Type DUPLEX 370 EC4.D and DUPLEX 370 are installed during the fall and run continuously for 9 months. The ventilation system is placed outside the house and provides filtered conditioned air to the child's bedroom, through insulated pipes mounted in a window opening. The window opening was built specifically for this purpose in form of a thermo plate replacing the window glass. The unit provides the bedroom with at least 2-3 air changes per hour. The placebo unit (DUPLEX 370) is a completely similar installation which only recirculates the air in the room instead of replacing it. We recommend all parents to wash the duvet and pillow every 3 months.

Data collection:

Data on the children's health is collected every 3 months when the families visit the outpatient clinics. The children are seen by specialist doctors.

At home visits, also every 3 months, data concerning the indoor air quality is collected.

연구 유형

중재적

등록 (실제)

46

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Region Hovedstaden
      • Herlev, Region Hovedstaden, 덴마크, 2730
        • Børneafdelingen Herlev Hospital
    • Region Midt
      • Aarhus, Region Midt, 덴마크, 8200
        • Childrens Department, Aarhus University Hospital
      • Herning, Region Midt, 덴마크, 7400
        • Childrens Department, Herning Hospital
      • Randers, Region Midt, 덴마크, 8930
        • Childrens DEpartment, Randers Hospital
    • Region Nordsjælland
      • Hillerød, Region Nordsjælland, 덴마크, 3400
        • Childrens Department, Hillerød hospital
    • Region Syddanmark
      • Kolding, Region Syddanmark, 덴마크, 6000
        • Childrens Department, Kolding Hospital
      • Odense, Region Syddanmark, 덴마크, 5000
        • H.C. Andersens Children Hospital, Odense University Hospital

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

5년 (어린이, 성인)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Doctors diagnosed asthma
  • Need of inhaled steroid titrated down to at least 400 microg/day of Budesonide or equivalent dose of other corticosteroid
  • Skin prick test >/= 3 mm or specific IgE >/= 0,7 kU/l to house dust mites (Derm. Pteronyssinus and/or Derm. Farinae)
  • more than 500 nanog/gr dust of house dust mite allergen in the childs mattress.
  • Living in a one-family house and will allow changes of the house during the intervention period.
  • Capable of giving informed consent.

Exclusion Criteria:

  • Other clinically relevant allergies to tree pollen or animals present in the house.
  • Other diseases or treatments, as for example immunotherapy, which could influence the results.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 네 배로

무기와 개입

참가자 그룹 / 팔
개입 / 치료
활성 비교기: Ventilation
Increased ventilation in the childs bedroom to at least 2-3 air changes pr hour.
The ventilation system is placed outside the house and provides filtered conditioned air to the child's bedroom, through insulated pipes mounted in a window opening. The window opening was built specifically for this purpose in form of a thermo plate replacing the window glass. The unit provides the bedroom with at least 2-3 air changes per hour
다른 이름들:
  • Ventilation units Type DUPLEX 370 EC4.D
위약 비교기: Placebo ventilation
Ventilation system that recirculates the air in the childs bedroom
The placebo unit (DUPLEX 370) is a completely similar installation to the active ventilation unit, but it only recirculates the air in the room instead of replacing it with fresh conditioned air.
다른 이름들:
  • Placebo ventilation unit type DUPLEX 370

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Changes in dose of inhaled corticosteroid
기간: Baseline, 3 months, 6 months and 9 months
Measured in micrograms of a specific inhaled corticosteroid
Baseline, 3 months, 6 months and 9 months
Changes in particle concentration in child bedroom
기간: baseline, 3 months, 6 months and 9 months
Measured as particles pr. m3
baseline, 3 months, 6 months and 9 months

2차 결과 측정

결과 측정
측정값 설명
기간
FEV1
기간: Baseline, 3,6 and 9 months
Forced Expiratory Volume after 1 second
Baseline, 3,6 and 9 months
FeNO
기간: Baseline, 3,6 and 9 months
Forced Expiratory Nitric Oxide
Baseline, 3,6 and 9 months
Quality of Life
기간: Baseline, 3,6 and 9 months
Pediatric Asthma Quality of Life Questionaire
Baseline, 3,6 and 9 months
Standard Skin-prick-test and Specific IgE- phadiatop
기간: Baseline and 9 months
Reduction in diameter of skin-prick-test for standard inhalant allergens and reduction in specific IgE for standard inhalant allergens measured in kU/l.
Baseline and 9 months
Asthma Symptoms
기간: During 14 days at baseline, 3, 6 and 9 months
Assessed from a Symptom score scheme
During 14 days at baseline, 3, 6 and 9 months
Peakflow variability
기간: Baseline, 3, 6 and 9 months
Baseline, 3, 6 and 9 months
Ventilation rate
기간: Baseline, 3, 6 and 9 months
Ventilation rate in the childs bedroom and in the Whole house
Baseline, 3, 6 and 9 months
Physical conditions in the child bedroom and whole house
기간: baseline, 3 6 and 9 months
Changes in temperature and humidity
baseline, 3 6 and 9 months
Allergens in child mattress and airborne in child bedroom
기간: baseline, 3, 6 and 9 months
Reduction in allergen levels.
baseline, 3, 6 and 9 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 책임자: Torben Sigsgaard, Professor, Aarhus University, Department of Public Health, Section for Environment, Occupation and Health
  • 수석 연구원: Nina V Hogaard, MD, Aarhus University, Dept. of Public Health, Section for Environment, Occupation and Health

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2012년 8월 1일

기본 완료 (실제)

2016년 2월 1일

연구 완료 (실제)

2016년 2월 1일

연구 등록 날짜

최초 제출

2014년 2월 19일

QC 기준을 충족하는 최초 제출

2014년 2월 19일

처음 게시됨 (추정)

2014년 2월 21일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2016년 5월 12일

QC 기준을 충족하는 마지막 업데이트 제출

2016년 5월 11일

마지막으로 확인됨

2016년 5월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

Ventilation에 대한 임상 시험

구독하다