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European Lung Foundation
Our core content on Lung conditions and related factsheets has been translated to a number of other languages by our volunteer team.
For more languages explore all available Factsheet translations.
Volunteer as a translator or learn how to translate using Chrome, Firefox or Edge browsers.
Home » Get involved » Surveys » Developing research on nocturnal oxygen therapy in pulmonary fibrosis
This survey is anonymous and will help to improve the treatment of people living with pulmonary fibrosis.
This survey has been developed by Monash University. The aim of the survey is to gather information about the effects of nocturnal oxygen therapy and improve its use in people living with pulmonary fibrosis.
Any person living with pulmonary fibrosis can participate in the survey.
Approximately 1 in 3 people living with pulmonary fibrosis have a low oxygen level in their sleep, and this is associated with a reduced quality of life. However, little is known about assessing low oxygen levels during sleep, or the effects of using nocturnal oxygen therapy. The aim of the survey is to establish a global perspective of patients and caregivers on issues relating to the use of nocturnal oxygen therapy in pulmonary fibrosis.
If you want to learn more about the survey, please click on the links to be taken to the survey. If you choose to take part, you will complete a short questionnaire asking your views on the use and research about nocturnal oxygen therapy in pulmonary fibrosis.
This survey is anonymous and you can leave the survey at any time.
Please note the deadline for responses is the 13 October 2024.
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European Lung Foundation's TR ID number in the Transparency Register is: 094039644810-79
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