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WithdrawnNCT02775487Updated Sep 30, 2016

Smog Induced Indoor Air Pollution in Homes of Chronic Obstructive Pulmonary Disease Patients.

An observational study in Chronic Obstructive Pulmonary Disease, sponsored by University of Missouri-Columbia. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-09-30.

Sponsored by University of Missouri-Columbia · Observational

Why this study was withdrawn
Withdrawn before IRB review. Investigator no longer working at facility.
Study type
Observational
Model
Ecologic or community
Time perspective
Prospective
Enrollment
0
Ages
18 Years and older
Sex
All
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Study summary

Primary objective of this project is to measure the impact of passive control and active control systems on indoor pollution that is directly or indirectly related to ambient air pollution (smog). The first goal will be to measure baseline parameters for 50 homes, including information about the building, ventilation characteristics, pollution levels (indoors and outdoors), and occupant survey information. In a subset of these homes, either passive or active control systems will be installed and the impact of these systems on indoor concentrations. Participants will be enrolled on a rolling basis (5-15 persons studied at a given point in time) over a 16-month period. Participants will be followed for approximately 5 weeks and data obtained at three points in time: at enrollment (day 1 of study), after 1 week (baseline verification) and after four weeks with the control system in the home (at the end of study week 5).

Read the detailed description

Chronic obstructive pulmonary disease (COPD) is a degenerative lung disease resulting in lower lung function characterized by an obstruction to airflow. COPD is an umbrella term for two disease processes: chronic bronchitis and emphysema. It is currently the 4th leading cause of death in the United States. Approximately 14 million Americans are known to suffer from COPD; however, it is estimated that as many as 24 million Americans may have some form of one or both of the diseases (Centers for Disease Control, 2011). The primary risk factor for developing COPD is cigarette smoking; other factors include exposure to air pollution, occupational dusts and chemicals, and lower socioeconomic status. Poverty has been identified as a risk factor for COPD but the aspects related to poverty that increase the risk of COPD are unclear (GOLD, 2011). Lower education level and household income has been noted to relate to increased severity of COPD (Eisner, Blanc, Omachi, Yelin, Sidney, Katz, et al, 2011). An American Lung Association survey found that over half of those diagnosed with COPD reported that their condition limits their ability to perform activities of daily living, including activities in the home (American Lung Association, 2009). As air pollution can lead to an exacerbation of COPD symptoms and precipitate emergency room visits and hospitalization, minimizing pollution in indoor air may be a key component of disease management and decreasing health care costs.

02

Conditions studied

  • Chronic Obstructive Pulmonary Disease

Keywords

  • COPD
  • Air quality
03

In context

Pulmonary Disease, Chronic Obstructive

4,252 studies on the registry are indexed under Pulmonary Disease, Chronic Obstructive; 707 are open to participants now.

Browse Pulmonary Disease, Chronic Obstructive studies →

Lead sponsor

University of Missouri-Columbia is the lead sponsor of 364 studies on the registry; 70 are open to participants now.

Of its 42 completed or terminated interventional studies of FDA-regulated products, 29 (69%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Study participants will be recruited from pulmonary rehabilitation centers in St. Louis, MO. Potential participants will be screened to ascertain eligibility based on diagnosis and stage of disease progression.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • diagnosis of COPD (stage III or IV); adults over the age of 18 years

Exclusion criteria

Exclusion Criteria:

  • Children (persons under age 18), fetuses, neonates, pregnant women, prisoners
05

Study design

Observational model
Ecologic or community
Time perspective
Prospective
Enrollment
0 participants (actual)

Groups and cohorts

  • COPD and air quality

    Persons enrolled in the study will have been diagnosed with Stage III or IV COPD and samples of air taken from their home environment.

06

What researchers measure

Primary outcomes

  1. Change in Air quality measures at week 5

    Air samples taken from the home

    Time frame: week 5 of study

Secondary outcomes

  1. Change in Borg scale for breathlessness from week 1 to week 5

    Scale on which participant rates perceived breathlessness

    Time frame: week 1 of study, week 2 of study and week 5 of study

  2. Change in vital signs from week 1 to week 5

    Heart rate, respiratory rate, blood pressure, oxygen saturation (SpO2) via pulse oximetry, bedside spirometry

    Time frame: week 1 of study, week 2 of study and week 5 of study

  3. Change in Air quality measures from week 1 to week 5

    Change in Air quality measures from week 1 to week 5

    Time frame: week 1 and week 2 of the study

07

Study locations

1 site
  • University of Missouri
    Columbia, Missouri 65211, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2013, a primary completion of Jan 2013 and a completion of Jan 2013. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 23, 2012
First posted
May 17, 2016
Start
Jan 2013
Primary completionEst.
Jan 2013
CompletionActual
Jan 2013
Last update
Sep 30, 2016
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 30, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02775487
Responsible party
Sponsor
First posted
May 17, 2016
Start date
Jan 2013
Primary completion
Jan 2013 (estimated)
Completion
Jan 2013
Last update
Sep 30, 2016

Study contacts

Shawna L Strickland, PhD, RRT
principal investigator · University of Missouri-Columbia

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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