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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04497753
Other study ID # 2020-KZLXB-02-02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 19, 2020
Est. completion date August 31, 2020

Study information

Verified date October 2020
Source Fuwai Yunnan Cardiovascular Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study was to explore the relationship between the transmission of respiratory diseases and the correct wearing of masks, as well as the factors affecting the correct wearing of masks. The research is beneficial to the prevention of respiratory diseases and moves the barrier of prevention and control forward. It is of great significance to COVID-19 's practical prevention and control.


Description:

1. Overall design:This study uses the methods of cross-sectional survey and chance sampling. 2. Sign the Informed Consent Form. 3. Investigation on the basic situation of personnel: The gender, age and education level of the subjects were analyzed as the factors influencing whether the mask was worn correctly or not. 4. Investigation on the types of wearing masks: 1) The types of masks worn by the subjects were recorded as the basis of stratified statistics. 2) Mask suitability testing: 1. Visual inspection whether the mask is close to the face with obvious gaps. 2. Breathing test Are there any obvious gaps or whether the cotton around the mask is blown when the subject taking a deep breath. 3. Spray test The FT-30 qualitative fitness test system of 3M company was used to test the suitability and correctness of wearing mask. In the spray test, all subjects underwent a sensitivity test to prove their ability to smell the bitterness of the reagent, and then sensitive subjects can participate in the hood test.. In order to objectively reflect the overall situation of the subjects, it is necessary to cover many ages and educational levels of men and women.


Recruitment information / eligibility

Status Completed
Enrollment 6000
Est. completion date August 31, 2020
Est. primary completion date August 31, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 7 Years and older
Eligibility Inclusion Criteria: 1. Healthy people with autonomous behavior ability and language expression ability who are older than or equal to 7 years old, Persons under the age of 18 need to obtain the consent of their legal guardians; 2. The subjects and / or their legal guardians have the ability to understand the contents of the study and to participate in all the research processes with the subjects; 3. People who volunteered to take part in the study; 4. There was no respiratory infection in nearly one month. Exclusion Criteria: 1. People with a history of allergies, including those who are allergic to pollen, dust mites, etc; 2. People with any history of drug allergy; 3. People who have participated in the experiment are not allowed to participate in this study for the second time; 4. Pregnant women; 5. The healer after COVID-19 's infection; 6. After questioning, it was found that the subjects were the factors that affected the study, such as dysosmia, or those who had decreased olfactory ability due to disease, or facial paralysis, which affected the judgment of the test; 7. Those who are participating in clinical trials of other drugs / devices; 8. Subjects with poor compliance or unwilling to cooperate with the operation as required; 9. The researchers believe that any other situation that may affect the evaluation of the study.

Study Design


Locations

Country Name City State
China Fuwai hospital, Beijing Beijing Beijing
China Bin Health Wen Jinzhong Shanxi
China Fuwai Yunnan Cardiovascular Hospital Kunming Yunnan
China Luliang Health Bureau Qujing Yunnan
China Luoping Health Bureau Qujing Yunnan
China Shizong Health Bureau Qujing Yunnan
China Taizhou Health Bureau Taizhou Jiangsu
China Yuanqu Health Bureau Yuncheng Shanxi

Sponsors (1)

Lead Sponsor Collaborator
Fuwai Yunnan Cardiovascular Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary can or can't fell bitterness Whenever the subject feels bitter, it means that the mask does not fit well with the subject's face.
If the subjects do not feel bitter all the time, it means that the mask is suitable for the subjects' face and can be worn.
Immediately after spray test
See also
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Completed NCT04474028 - An Epidemiological Investigation on the Correct Wearing of Face Mask
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Recruiting NCT05965128 - Promotion and Application of a New Three-level Etiological Diagnosis Strategy for Fever Clinics in Respiratory Infectious Diseases