Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12620000908932
Ethics application status
Approved
Date submitted
23/07/2020
Date registered
14/09/2020
Date last updated
4/04/2024
Date data sharing statement initially provided
14/09/2020
Type of registration
Prospectively registered

Titles & IDs
Public title
Making it Personal: Identifying Personalised Triggers of Fatigue in Multiple Sclerosis
Scientific title
Making it Personal: Identifying Personalised Triggers of Fatigue in Multiple Sclerosis using N-of-1 studies
Secondary ID [1] 301860 0
None
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Multiple Sclerosis 318356 0
Condition category
Condition code
Neurological 316365 316365 0 0
Multiple sclerosis

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
Multiple sclerosis (MS) is a condition of the central nervous system, where there is interference in the nerve impulses within the brain, spinal cord and optic nerves. Scars occur within the central nervous system and depending on where they develop, manifest into various symptoms. Some symptoms include problems with motor control (muscle spasms, weakness, lack of coordination/balance and functioning of arms and legs) neuropsychological issues (memory loss and cognitive issues), bladder and bowel incontinence, and other neurological symptoms such as vertigo, pins and needles, neuralgia and visual disturbances. Fatigue is among the most commonly reported, most disabling but least understood symptom experienced by patients with MS. Patients differ substantially in the symptoms they experience depending on where lesions have developed on the brain and spinal cord. Factors such as physical activity, sleep, stress and mood may trigger, worsen or co-occur with symptoms.

In this study, participants will complete questionnaire items about fatigue and potential triggers (e.g. physical activity, sleep, stress, mood) on a daily basis for period of 6-18 weeks via an electronic diary with an inbuilt accelerometer. Questionnaire items related to personally-relevant symptoms (e.g. body pain) and potential triggers of fatigue (e.g. sleep) will be selected by participants at the start of the study and incorporated into to the design of the daily questionnaires. Brief questionnaires will be completed by participants three times per day (morning, afternoon and evening) and will take approximately 1-2 minutes to complete.
Intervention code [1] 318152 0
Not applicable
Comparator / control treatment
No control group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 324527 0
The severity of fatigue measured on a visual analogue scale ranging from 0 to 100. The measure is designed specifically for this study. The data is analysed at the individual (N-of-1) level.
Timepoint [1] 324527 0
Three times per day (morning, afternoon and evening) for 6-18 weeks (duration of data collection period based on the preference of the participant).
Secondary outcome [1] 384885 0
The severity of a personally-relevant symptom (e.g. body pain) selected by the participant at the start of the study measured on a visual analogue scale ranging from 0 to 100. The measure is designed specifically for this study. The data is analysed at the individual (N-of-1) level. If more than one symptom is selected by the participant, it will be analysed as another secondary outcome (i.e. not a composite measure).
Timepoint [1] 384885 0
Three times per day (morning, afternoon and evening) for 6-18 weeks (duration of data collection period based on the preference of the participant).
Secondary outcome [2] 385798 0
Acceptability of the study procedures
Timepoint [2] 385798 0
Semi-structured interviews will be conducted at the end of the study to explore participant views about the study procedures
Secondary outcome [3] 385799 0
Feasibility of study procedures
Timepoint [3] 385799 0
Feasibility will be assessed by calculating the recruitment/retention rate and completion rate of daily questionnaires during the study for each participant after the data collection period is completed.

Eligibility
Key inclusion criteria
Individuals who:
(1) have a diagnosis of multiple sclerosis, as confirmed by GP
(2) are aged 18 years or older
(3) live in Greater Brisbane
(4) have access to the internet to complete an online questionnaire
(5) are willing to complete brief questionnaires via an electronic diary each day for 6 weeks
(6) have a score on the Modified Fatigue Impact Scale above the age-, gender- and education-specific norm cut-offs
(7) have been on a stable dose of medication for at least 1 month, as confirmed by GP
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Individuals who have:
(1) acquired brain injury
(2) active psychiatric disorder (e.g. schizophrenia),
(3) cognitive impairment
(4) sleep disorder or
(5) other relevant progressive neurological disorders

The individual's GP will determine whether they meet any of the exclusion criteria.

Study design
Purpose
Natural history
Duration
Longitudinal
Selection
Defined population
Timing
Prospective
Statistical methods / analysis
Statistical power in N-of-1 studies is determined by the number of repeated measurements from the same individual. Therefore, there are no sample size requirements related to the number of participants recruited.

Individual level and aggregated analyses will be performed. Individual level analyses will be conducted using Bayesian time series analysis. Aggregated analyses will be conducted using Bayesian hierarchical models.

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
22/05/2023
Actual
16/02/2024
Date of last participant enrolment
Anticipated
31/08/2024
Actual
Date of last data collection
Anticipated
12/10/2024
Actual
Sample size
Target
20
Accrual to date
4
Final
Recruitment in Australia
Recruitment state(s)
QLD

Funding & Sponsors
Funding source category [1] 306282 0
Charities/Societies/Foundations
Name [1] 306282 0
MS Australia
Country [1] 306282 0
Australia
Primary sponsor type
University
Name
The University of Queensland
Address
General Practice Clinical Unit,
Medical School
The University of Queensland
Level 8, Health Sciences Building 901/813
Brisbane Qld 4029 Australia
Country
Australia
Secondary sponsor category [1] 306773 0
None
Name [1] 306773 0
Address [1] 306773 0
Country [1] 306773 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 306498 0
The University of Queensland Human Research Ethics Committee
Ethics committee address [1] 306498 0
Ethics committee country [1] 306498 0
Australia
Date submitted for ethics approval [1] 306498 0
07/07/2020
Approval date [1] 306498 0
10/07/2020
Ethics approval number [1] 306498 0
#2018000741

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

Contacts
Principal investigator
Name 104074 0
Dr Suzanne McDonald
Address 104074 0
General Practice Clinical Unit,
Medical School
The University of Queensland
Level 8, Health Sciences Building 901/813
Brisbane Qld 4029 Australia
Country 104074 0
Australia
Phone 104074 0
+61 7 334 65136
Fax 104074 0
Email 104074 0
[email protected]
Contact person for public queries
Name 104075 0
Suzanne McDonald
Address 104075 0
General Practice Clinical Unit,
Medical School
The University of Queensland
Level 8, Health Sciences Building 901/813
Brisbane Qld 4029 Australia
Country 104075 0
Australia
Phone 104075 0
+61 7 334 65136
Fax 104075 0
Email 104075 0
[email protected]
Contact person for scientific queries
Name 104076 0
Suzanne McDonald
Address 104076 0
General Practice Clinical Unit,
Medical School
The University of Queensland
Level 8, Health Sciences Building 901/813
Brisbane Qld 4029 Australia
Country 104076 0
Australia
Phone 104076 0
+61 7 334 65136
Fax 104076 0
Email 104076 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
Data collected for participants underlying published results will be made available.
When will data be available (start and end dates)?
Immediately following publication; no end date
Available to whom?
Only researchers who provide a methodologically sound proposal
Available for what types of analyses?
For IPD meta-analyses
How or where can data be obtained?
Access subject to approvals by Principal Investigator (Dr Suzanne McDonald; [email protected])


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.