Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
UNKNOWN
Clinical Phase
NA
Total Enrollment
106 participants
Study Classification
INTERVENTIONAL
Study Start Date
2022-07-21
Study Completion Date
2024-12-31
Brief Summary
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Despite the known benefits of physical activity, the majority of Canadians fail to meet recommended guidelines. Patients with axial spondyloarthritis (axSpA) also fail to meet recommended guidelines. Exercise, a critical component of physical activity, is considered the cornerstone of axSpA management. Simple health technologies such as mobile phone messaging and email can be useful tools to increase engagement in regular physical activity among the general public and patients with chronic disease. As such, the aim of this research project is to develop and test a patient-centered strategy that provides education on the importance of physical activity and utilizes existing health technologies (such as smart phone applications) to encourage regular participation in physical activity. The results of this study are expected to demonstrate that patients with axSpA will increase their daily engagement in physical activity, and therefore improve symptoms, function and overall quality of life.
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Detailed Description
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Conditions
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Axial Spondyloarthritis
Study Design
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Allocation Method
RANDOMIZED
Intervention Model
PARALLEL
Repeated measures randomized control pre-test/post-test design comparing an intervention group with a control group (usual care).
Primary Study Purpose
TREATMENT
Blinding Strategy
NONE
Study Groups
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Intervention Group
Participants randomized to the intervention group will receive an initial electronic communication (i.e. email) that includes:
* Link to physical activity education. This will be an educational module based on Phase 1 results and evidence-based literature regarding the benefits of physical activity in the general population and specific to axSpA.
* One week after receiving the physical activity educational module, participants will receive access to the ADAS application and an .ics file for each 3-week cycle of electronic calendar reminders to engage in physical activity.
Group Type
EXPERIMENTAL
Health technology-based intervention strategy
Intervention Type
OTHER
Patient-centered, technology-based intervention strategy aimed at increasing physical activity in patients with axSpA
Control Group
Participants randomized to the control group will receive usual care, which includes standard rheumatology care and access to educational materials on the importance of exercise and physical activity available through the TWH Spondylitis Program and through the public domain. They will receive a link to the physical activity educational module at baseline. They also have access to the program physiotherapist for a single one-hour individualized exercise consultation as requested by either the patient or the treating rheumatologist.
Group Type
NO_INTERVENTION
No interventions assigned to this group
Interventions
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Health technology-based intervention strategy
Patient-centered, technology-based intervention strategy aimed at increasing physical activity in patients with axSpA
Intervention Type
OTHER
Eligibility Criteria
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Inclusion Criteria
* Adults (aged 18 and older) with a diagnosis of axSpA based on ASAS criteria
* Have access to email and a smart phone device (Android or iOS operating systems)
* Enrolled in the SPARCC Research Program
* Passes pre-participation health screen
* Have access to email and a smart phone device (Android or iOS operating systems)
* Enrolled in the SPARCC Research Program
* Passes pre-participation health screen
Exclusion Criteria
* Non-English speaking
* Not enrolled in the SPARCC Research Program
* Comorbidities or physical impairments that may preclude physical activity (e.g., symptomatic cardiovascular disease; wheelchair bound etc.)
* Not enrolled in the SPARCC Research Program
* Comorbidities or physical impairments that may preclude physical activity (e.g., symptomatic cardiovascular disease; wheelchair bound etc.)
Minimum Eligible Age
18 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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Canadian Initiative for Outcomes in Rheumatology Care
OTHER
Sponsor Role
collaborator
University Health Network, Toronto
OTHER
Sponsor Role
lead
Responsible Party
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Laura Passalent
Physiotherapist Practitioner
Responsibility Role
PRINCIPAL_INVESTIGATOR
Principal Investigators
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Laura Passalent
Role: PRINCIPAL_INVESTIGATOR
University Health Network, Toronto
Locations
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University Health Network - Toronto Western Hospital
Toronto, Ontario, Canada
Site Status
RECRUITING
Countries
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Canada
Central Contacts
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Facility Contacts
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References
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1. World Health Organization. Fact Sheet Updated February 2018. Available at: http://www.who.int/mediacentre/factsheets/fs385/en/ Accessed on March 26, 2018
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Other Identifiers
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19-5919
Identifier Type: -
Identifier Source: org_study_id
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