Evaluating the Impact of Chronic Rhinosinusitis on the Health-Related Quality of Life Among Adults With Cystic Fibrosis

St. Paul's Hospital, Canada

Status: Completed

Conditions: Cystic Fibrosis

Treatments: Behavioral: Cystic Fibrosis Questionnaire (Revised) for Teens/Adults

Study type: Observational

Funder types: Other

Identifiers

NCT02003079

CFSinus-001

Details and patient eligibility

About

Individuals with Cystic Fibrosis (CF) have a defective protein, which is known as the cystic-fibrosis transmembrane regulator (CFTR). The CFTR transports salt and hydrates mucous. CFTR defects may result in the accumulation of thick mucous in the sinus cavities. As a result, the tiny hair-like structures that sweep mucous out of the sinuses cannot function properly, which can lead to recurrent infection and swelling of the sinus walls. When symptoms are persistent for more than 12 weeks, this is known as chronic rhinosinusitis (CRS). The symptoms that are associated with CRS are nasal discharge, congestion, facial pain or pressure and reduced sense of smell. CRS in non-CF patients affects a large number of individuals in Canada and has been found to be associated with poor quality of life. In the CF population the life expectancy is increasing but chronic disease like CRS is becoming increasingly prevalent. Investigators currently do not know the impact that CRS has on the health-related quality of life in adults with CF and how many suffer from symptoms. The investigators aim to determine the impact of CRS among adults with CF, in order to gain a better understanding of chronic disease among these individuals. The investigators strongly feel this research will improve the referral processes between Respirologists and Otolaryngologists, thereby improving treatment and quality of life for patients.

Enrollment: 113 patients

Sex: All

Ages: 19+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 19 years of age or older
• Definitive diagnosis of cystic fibrosis from positive genetic or sweat chloride test
• Currently enrolled at the St. Paul's Cystic Fibrosis Clinic

Exclusion criteria

• Individuals unable to understand the purpose, methods and conduct of this study.
• Patients unwilling to provide informed consent.

Trial design

113 participants in 1 patient group

Diagnosed with or without Chronic Rhinosinusitis

Treatment:

Behavioral: Cystic Fibrosis Questionnaire (Revised) for Teens/Adults