The Clinical Trials team is collaborating with Clinical Affairs and the CF Foundation Mental Health Advisory Committee to develop research priorities in mental health for people with CF and their caregivers. The purpose of the survey is to inform the framework that will guide future funding decisions. This framework will also be included on our Key Priorities page as a resource to researchers.

Completion of the survey is expected to take about 8-10 minutes, but you are free to refuse or to withdraw at any time. Participation is completely voluntary and there are no known risks or benefits to participation. Completing this survey implies consent. Your information and opinions are confidential, nothing you say will be attached to your name. To ensure that we can share our learnings, your anonymized responses to these questions may be included and/or aggregated for the purposes of research, education, or program communications.
 
6% of survey complete.

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