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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02898129
Other study ID # CHUB-CRD-Housing
Secondary ID
Status Completed
Phase N/A
First received September 8, 2016
Last updated August 3, 2017
Start date September 2016
Est. completion date July 2017

Study information

Verified date August 2017
Source Brugmann University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The research question is "Are the different types of house in Ho Chi Minh city equally contributing to chronic respiratory diseases?".

According to this question, a cross-sectional and explorative study was set up to explore the differences in the environmental characteristics and prevalence of chronic respiratory diseases among common housing types in Ho Chi Minh city. Preliminary work was performed in 100 houses (20 houses per type, included tube houses, rental houses, rural houses, slum and apartment) from November 2013 to June 2015. It included measures by environmental devices, questionnaires and indoor activities diaries.

This study will aim to collect information about the prevalence of chronic respiratory diseases (CRDs) inside those house types to understand more about role of house types in developing CRDs.

The objective is:

1. to evaluate the relationships between the type of house and lung function of inhabitants in each housing type.

2. to evaluate the effects of environmental risk factors in each house type on prevalence of CRDs


Recruitment information / eligibility

Status Completed
Enrollment 1500
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 10 Years to 65 Years
Eligibility Inclusion Criteria:

- Everybody

Exclusion Criteria:

- Not able to answer the questionnaire or give informed consent

- Have a contra-indication for lung function test (acute myocardial infarction less that 1 month ago, pain related to spirometry, dementia/confused)

Study Design


Intervention

Other:
Questionnaire

Device:
Lung function test
Basic lung function test performed with a micro-spirometer, without broncho dilatator

Locations

Country Name City State
Vietnam Pham Ngoc Thach University of medicine Ho Chi Minh City

Sponsors (1)

Lead Sponsor Collaborator
Brugmann University Hospital

Country where clinical trial is conducted

Vietnam, 

References & Publications (35)

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* Note: There are 35 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary FEV1/FVC Basic lung function test, without broncho dilatation (micro-spirometer). All lung function related outcomes are performed during the same test. FEV1: forced expiratory volume in one second. FVC: Forced vital capacity. 5 minutes
Primary FVC Basic lung function test, without broncho dilatation (micro-spirometer). All lung function related outcomes are performed during the same test.FVC: Forced vital capacity. 5 minutes
Primary VC Basic lung function test, without broncho dilatation (micro-spirometer). All lung function related outcomes performed during the same test. VC: Vital capacity 5 minutes
Primary FEF 25-75% Basic lung function test, without broncho dilatation (micro-spirometer).All lung function related outcomes are performed during the same test. FEF: Forced expiratory flow 5 minutes
Primary Socio-demographic status Socio-demographic data, assessed by a home made questionnaire around 10 minutes
Primary Health status Health status (symptomatology) data, assessed by a home made questionnaire around 10 minutes
Primary Indoor air exposure time Indoor air exposure (time spent indoor within housing types, with associated air characteristics) data, assessed by a home made questionnaire around 10 minutes
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