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Trial registered on ANZCTR
Registration number
ACTRN12624000385549
Ethics application status
Approved
Date submitted
7/03/2024
Date registered
3/04/2024
Date last updated
21/05/2024
Date data sharing statement initially provided
3/04/2024
Type of registration
Prospectively registered
Titles & IDs
Public title
Investigating smartphone tracking apps for people with Irritable Bowel Syndrome
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Scientific title
Investigating smartphone tracking apps for people with Irritable Bowel Syndrome
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Secondary ID [1]
311689
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none
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Irritable bowel syndrome
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Condition category
Condition code
Oral and Gastrointestinal
329848
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The intervention of this study is the use of a symptom tracking app. In particular the study will use the Eat Smart Kiwi app which is available on the Apple and Android app stores. There will be two intervention groups that differ in terms of dose effect. One group will be asked to track a large list of symptoms including common symptoms like headache and fatigue. The second group will only be asked to track symptoms relevant to irritable bowel syndrome like stomach pain. Tracking symptoms involves rating the symptom on a scale from great - 0 to awful -10. The time at which they make this rating is recorded or they can adjust this to reflect the time at which they are making the rating for. The app has options to set up to three reminders per day (9am, 1pm, 7pm) we will make participants aware of this feature but not require them to use a reminder. All groups will be asked to use the app for four weeks. In addition to symptom tracking the app has features to track diet, sleep, mood and bowel movements. We will encourage them to use the diet tracking feature to fit with the trial's cover story. Food tracking involves setting the time of eating and listing the different foods eaten. The app does not support calorie tracking, just noting the food itself. There will be no requirement to use any of the other features. We will monitor adherence by extracting data regarding the number of times the app was opened within the four week period. We will not access any of the data input to the app regarding symptoms or food.
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Intervention code [1]
328150
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Treatment: Devices
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Comparator / control treatment
Participants in the control group will also download the Eat Smart Kiwi app and use it for one month. However the symptom tracking function of the app will be disabled.
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Control group
Active
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Outcomes
Primary outcome [1]
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Symptom reporting
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Assessment method [1]
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Side Effect Attribution Score - modified to link symptoms to IBS rather than medication.
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Timepoint [1]
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Baseline, two weeks, four weeks, six months post end of app usage period
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Secondary outcome [1]
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Gastrointestinal symptom-specific anxiety
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Assessment method [1]
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Assessed using the visceral symptoms index (VSI)
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Timepoint [1]
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baseline, two weeks, four weeks and six months post end of app usage period
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Secondary outcome [2]
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general anxiety
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Assessment method [2]
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Assessed using state trait anxiety inventory six item form (STAI-6)
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Timepoint [2]
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Baseline, two weeks, four weeks and six months post end of app usage period
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Eligibility
Key inclusion criteria
Participants must either have a diagnosis of Irritable Bowel Syndrome (IBS) or meet the Rome IV criteria for an IBS diagnosis.
Additionally participants must have a smartphone and be able to read and write in English.
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Minimum age
18
Years
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Maximum age
80
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
People unwilling to use a food tracking app for four weeks.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Participants will be randomised to one of three groups automatically by computer when they complete the screening questionnaire.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation using a randomisation table created by computer software
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
30/04/2024
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Actual
30/04/2024
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Date of last participant enrolment
Anticipated
31/05/2024
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Actual
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Date of last data collection
Anticipated
10/02/2025
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Actual
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Sample size
Target
140
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Accrual to date
3
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Final
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Recruitment outside Australia
Country [1]
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New Zealand
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State/province [1]
26191
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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University of Auckland
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Address [1]
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Country [1]
316017
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New Zealand
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Primary sponsor type
Hospital
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Name
Te Whatu Ora
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Address
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
318169
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Central Health and Disability Ethics Committee
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Ethics committee address [1]
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https://ethics.health.govt.nz/about/central-health-and-disability-ethics-committee/
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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28/03/2024
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Approval date [1]
314840
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26/04/2024
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Ethics approval number [1]
314840
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2024 EXP 19213
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Summary
Brief summary
This study intends to understand the effects of symptom tracking apps on symptom reporting for people with IBS. Participants will be allocated to use one of three versions of a smartphone tracking app that differs in terms of the degree of symptom reporting for four weeks. We expect that those asked to track more symptoms by the app may end up reporting experiencing more symptoms at the end of four weeks.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Kate MacKrill
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Address
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University of Auckland, 85 Park Road, Grafton, Auckland 1023
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Country
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New Zealand
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Phone
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+64 0212878834
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Grace Lyon
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Address
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University of Auckland, 85 Park Road, Grafton, Auckland 1023
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Country
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New Zealand
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Phone
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+64210756024
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Grace Lyon
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Address
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University of Auckland, 85 Park Road, Grafton, Auckland 1023
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Country
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New Zealand
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Phone
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+64210756024
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Fax
132892
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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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.
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