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Trial registered on ANZCTR


Registration number
ACTRN12618001859279
Ethics application status
Approved
Date submitted
12/11/2018
Date registered
15/11/2018
Date last updated
15/11/2018
Date data sharing statement initially provided
15/11/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Self-reported daytime sleepiness and sleep-disordered breathing in patients with Atrial Fibrillation
Scientific title
Self-reported daytime sleepiness and sleep-disordered breathing in patients with Atrial Fibrillation
Secondary ID [1] 296053 0
Nil known
Universal Trial Number (UTN)
Trial acronym
Snooze AF
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Atrial Fibrillation
 310376 0
Sleep-Disordered Breathing 310377 0
Condition category
Condition code
Cardiovascular 309097 309097 0 0
Other cardiovascular diseases
Respiratory 309098 309098 0 0
Sleep apnoea

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
Patients with a atrial fibrillation, a common heart rhythm abnormality, are often referred for formal sleep studies (polysomnography) to assess for the presence and severity of sleep-disordered breathing. Sleep-disordered breathing, of which sleep apnoea is an important subtype, is a known risk factor for developing atrial fibrillation and its treatment can improve the likelihood of maintaining normal sinus rhythm following atrial fibrillation treatment. One of the main clinical consequences of sleep-disordered breathing is excessive daytime sleepiness which can be assessed using questionnaires. The polysomnography tests are usually performed overnight in a specialised sleep centre and are reported by a qualified sleep technician and a respiratory physician. The duration of observation spans over the recruitment period which is from January 2012 to March 2017.
The electronic health records of the study patients will be examined and the following parameters (already present health records) retrieved for analysis: medical background (clinical history), antrhopometric data (weight, height and BMI), medication history, echocardiographic data, clinical questionnaires (AF severity questionnaires and sleepiness questionnaires) as well as the formal polysomnography reports. These data are already present in electronic format in medical records and will be accessed to retrieve the relevant information for the study once approved.
Intervention code [1] 312888 0
Diagnosis / Prognosis
Comparator / control treatment
Formal polysomnography tests are assessed by a respiratory physician and a diagnosis of the presence and severity of sleep-disordered breathing is made. Patients with sleep-disordered breathing will function as the main study group, and those without will be the controls.
The clinical data will be retrieved from the Centre for Heart Rhythm Disorders and Royal Adelaide Hospital over the period of the study, January 2012 to March 2017.
Control group
Historical

Outcomes
Primary outcome [1] 308070 0
Diagnosis of sleep-disordered breathing as quantified by polosymnography
Timepoint [1] 308070 0
At time of polysomnography
Secondary outcome [1] 353871 0
Excessive Daytime Sleepiness (quantified using the Epworth Sleepiness Scale)
Timepoint [1] 353871 0
At time of undergoing polysomnography

Eligibility
Key inclusion criteria
• Age equal to or greater than 18 years
• Diagnosed with paroxysmal or persistent atrial fibrillation (according to the 2017 HRS/EHRA/ECAS/APHRS/SOLAECE expert consensus statement on catheter and surgical ablation of atrial fibrillation.
• Referred to, and completed, a formal overnight polysomnography (PSG)
• Completed a contemporaneous Epworth Sleepiness Scale questionnaire
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
• Insufficient polysomnography data (less than 4 hours of sleep study or absence of measured apnoea-hypopnoea index reporting).
• Incomplete Epworth Sleepiness Scale score
• Pregnancy

Study design
Purpose
Screening
Duration
Cross-sectional
Selection
Defined population
Timing
Retrospective
Statistical methods / analysis
Clinical characteristics and relevant data from polysomnography, including apnoea-hypopnoea index (AHI), in addition to Epworth Sleepiness Scale (ESS) will be retrieved from Electronic Medical Reports (EMRs). Statistical analysis will be performed using SPSS statistical software for Windows (Version 24; IBM corp.). Following the reporting of descriptive statistics, the correlation between ESS and AHI will be tested using the Pearson correlation coefficient testing. The utility of ESS to predict SDB will be tested using the receiver-operating-characteristic (ROC) analysis and presented as area-under-the-curve (AUC). A binary logistic regression model that would utilise the available clinical features will be constructed to try and identify patients with significant sleep-disordered breathing.

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
3/12/2018
Actual
Date of last participant enrolment
Anticipated
10/12/2018
Actual
Date of last data collection
Anticipated
1/01/2019
Actual
Sample size
Target
300
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
SA
Recruitment hospital [1] 12388 0
The Royal Adelaide Hospital - Adelaide
Recruitment postcode(s) [1] 24653 0
5000 - Adelaide

Funding & Sponsors
Funding source category [1] 300641 0
University
Name [1] 300641 0
University of Adelaide
Country [1] 300641 0
Australia
Primary sponsor type
Individual
Name
Professor Prashanthan Sanders
Address
Director, Centre for Heart Rhythm Disorders
NHMRC Practitioner Fellow,
Knapman-NHF Chair of Cardiology Research,
University of Adelaide | SAHMRI
Director, Cardiac Electrophysiology & Pacing,
Royal Adelaide Hospital
Port Road
SA 5000
Country
Australia
Secondary sponsor category [1] 300777 0
None
Name [1] 300777 0
Address [1] 300777 0
Country [1] 300777 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 301430 0
Central Adelaide Local Health Network (CALHN) Research Ethics Committee
Ethics committee address [1] 301430 0
Ethics committee country [1] 301430 0
Australia
Date submitted for ethics approval [1] 301430 0
27/08/2018
Approval date [1] 301430 0
12/11/2018
Ethics approval number [1] 301430 0
R20180831

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 86966 0
Prof Prashanthan Sanders
Address 86966 0
Royal Adelaide Hospital
Cardiology 4G751-769
The University of Adelaide
Port Rd, SA 5000
AUSTRALIA
Country 86966 0
Australia
Phone 86966 0
+61 8 8313 9000
Fax 86966 0
Email 86966 0
prash.sanders@adelaide.edu.au
Contact person for public queries
Name 86967 0
Kadhim Kadhim
Address 86967 0
Royal Adelaide Hospital
Cardiology 4G751-769
The University of Adelaide
Port Rd, SA 5000
AUSTRALIA
Country 86967 0
Australia
Phone 86967 0
+61 8 8313 9000
Fax 86967 0
Email 86967 0
kadhim.kadhim@adelaide.edu.au
Contact person for scientific queries
Name 86968 0
Kadhim Kadhim
Address 86968 0
Royal Adelaide Hospital
Cardiology 4G751-769
The University of Adelaide
Port Rd, SA 5000
AUSTRALIA
Country 86968 0
Australia
Phone 86968 0
+61 8 8313 9000
Fax 86968 0
Email 86968 0
kadhim.kadhim@adelaide.edu.au

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.