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临床试验/NCT05843045
NCT05843045进行中(未招募)不适用

Indoor Air Quality Asthma Study: A Cooperative Study Between Coepland LP, Cairify, and Dayton Children's Hospital to Determine the Effect of Indoor Air Quality and Mitigation of Indoor Air Quality on Persistent Asthma

Dayton Children's Hospital2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2023年8月18日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
10
试验地点
2
主要终点
Asthma Control Test questionnaire

研究概览

简要总结

The primary objective is to determine whether continuous sensing, control and mitigation of home indoor air quality influences the frequency of asthma related symptoms, as measured by Serum IgE, Spirometry with exhaled Nitric Oxide, missed school and workdays, need for pharmacologic intervention (albuterol, oral steroids), frequency of sick visits to pulmonologist or primary care provider (PCP), urgent care / emergency department visits, and hospitalizations

详细描述

Participants will be in the research study for approximately 2 years. There will be 11 visits to the clinic for monitoring of asthma symptoms and pulmonary function and 16 interval contacts with research staff made by either telephone or email to monitor asthma symptoms. There will also be 5 visits to participants' homes by technicians from Emerson Climate Technologies and/or an electrician in cooperation with Emerson. During these visits Emerson employees will assess participants' homes to determine if they qualify for the study and install study equipment to monitor air quality for the first half of the study and monitor and mitigate air quality for the second half of the study. At the end of the study, the technicians and/or electrician from Emerson will reset the study equipment or replace participants' original equipment, if that is their wish.

Participants will be enrolled in the research study for approximately 2 years. The first year, technicians from the study sponsor will install indoor air quality monitoring equipment in the participants' homes and information about the air quality in their home as well as baseline health and asthma information will be collected. This will be done through continuous sensing via an Atmocube air quality sensor, and a portable air quality sensor, the Atmotube. Beginning in the second half of the study, mitigation strategies of a smart home thermostat, the Sensi Touch Smart Thermostat, a smart bath fan control, the Enbrighten Z-wave Switch, and high quality furnace filter, 3M Filtrete MPR 2800 Ultrafine Particle Reduction Air Filter, will be employed. Information about the participants' asthma, health status, and air quality in the homes will continue to be collected.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

盲法说明

All participants, care providers, and investigators will be blinded to the indoor air quality data as it is collected and the responses of the indoor air quality to mitigation.

入排标准

年龄范围
5 Years 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Child aged 5.0-15.9 years at the time of informed consent with mild, moderate, or severe persistent asthma diagnosis. In addition, participants
  • Agree to attend visits as outlined by protocol
  • Agree to respond to Asthma Control Test (ACT) and asthma control questions as outlined in protocol by telephone call, text, or email.
  • Are willing to comply with asthma treatment plan prescribed by physician.
  • Are willing to practice an acceptable form of birth control to avoid pregnancy. Acceptable forms of birth control include: true abstinence, male or female condom with or without spermicide, female barrier contraception (such as diaphragm, cervical cap, or sponge) with spermicide, continuous use of an intrauterine device throughout the study, hormonal contraceptives (including oral, patch, implanted, or injected), if used consistently and correctly throughout the study.
  • Reside in single-family dwellings and must either be homeowners or have written permission from their landlords to participate in the study.
  • In order to participate in the study, homes of participants must
  • have working ducted forced air HVAC systems
  • a 4-wire thermostat that is determined by Emerson technician to be capable of communicating with Sensi Touch Smart Thermostat
  • a bathroom fan switch with neutral wire and wall plate, controlling a bathroom fan that is vented to the outdoors
  • access to the internet with a modem or router.
  • A smartphone capable of pairing with the Atmotube Pro wearable sensor

排除标准

  • Exclusion criteria: Age <5.0 or >15.9 years at the time of informed consent, inability to commit to being in the same home for the length of the study, and/or not meeting the above inclusion criteria.

结局指标

主要结局

Asthma Control Test questionnaire

时间窗: Through study completion, approximately 2 years

Monthly Asthma Control Test by History. Possible scores ranging from 0 (worst control)-27 (best control) for patients ages 6-11 or 0 (worst control)- 25 (best control) for patients ages 12-16.

次要结局

  • weight(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)
  • respiratory rate(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)
  • Frequency of asthma Medication Use(Through study completion, approximately 2 years)
  • Physical examination(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)
  • height(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)
  • heart rate(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)
  • Number of asthma related visits to Primary Care Physician, Emergency Department or Urgent Care(Through study completion, approximately 2 years)
  • Number of missed school and work days(Through study completion, approximately 2 years)
  • Spirometry with exhaled nitric oxide(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)
  • Mini Paediatric Asthma Quality of Life Questionnaire (MiniPAQLQ)(Weeks 1, 49, 53, 105)
  • Concentration in serum of immunoglobulin E (IgE)(Weeks 1, 53, 105)
  • blood pressure(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)
  • oxygen saturation(Weeks 1, 13, 25, 37, 49, 53, 65, 77, 89, 101, 105)

研究者

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

Daniel Evans, MD

Chief, Pulmonary Medicine at Dayton Children's Hospital

Dayton Children's Hospital

研究点 (2)

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