- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03428893
Mobile Technology to Support Physical Therapy Exercise (MyTherEx)
MyTherEx: Mobile Technology to Support Physical Therapist Directed Exercise for People Aging With Arthritis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Osteoarthritis (OA) is the leading cause of disability in the U.S. The rate of activity limitation due to OA is progressing faster than expected while prevalence is projected to increase as a result of the obesity epidemic and population aging, making it a major public health problem. Exercise is an evidence-based treatment option that improves pain and disability outcomes in adults with osteoarthritis, but previous research has shown that adherence to prescribed exercise is low. Referral to physical therapy is common for people with OA with the standard of care including exercise prescription through paper handouts with brief instruction and static pictures. Such approaches do not incorporate known determinants of behavior change related to exercise adherence.
Recent technology products such as mobile applications (apps) for phones and tablets offer the potential to enhance communication between physical therapists and patients. The investigators aim to test a pragmatic intervention focused on supporting people with osteoarthritis to remain engaged with an exercise program. The specific aims of the project are to:
- Compare the effectiveness of mobile app supported exercise prescription to usual care (paper exercise prescription) on exercise adherence among mid-life and older adults receiving similarly dosed physical therapy for lower extremity OA. The investigators will also examine secondary outcomes of exercise self-efficacy, physical function, stiffness, and pain.
- Examine the feasibility and acceptability of mobile app supported exercise prescription through recruitment and retention rates, satisfaction with care ratings, and qualitative feedback.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Vermont
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South Burlington, Vermont, United States, 05407
- Dee Physical Therapy
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Self-report of healthcare provider diagnosed osteoarthritis in the hips or knees
- Ability to speak and read English
- No diagnosis of serious mental illness
- No diagnosis of serious or terminal illness (e.g., metastatic cancer, end stage renal failure)
- Access to smartphone/tablet
Exclusion Criteria:
- Cortisone injection to the joint with OA within the past 30 days
- Undergoing physical therapy post-total joint replacement or in preparation for total joint replacement in the next 3 months
- History of physical therapy for treatment of osteoarthritis in the past 6 months.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mobile Application Group
The mobile app group will receive physical therapy as determined by the physical therapist and agree to receive the home exercise prescription using a mobile app on their phone or personal tablet
|
Participants will receive usual care physical therapy guided by Clinical Practice Guidelines and based on individual symptoms and need over 7 in-person visits.
Measures will be collected by the physical therapist related to leg strength, balance, fitness, and mobility as part of the usual care physical therapy evaluation and follow-up.
The treating physical therapist will negotiate the physical therapy intervention based on patient preferences and goals and assessment findings.
Using clinical practice guidelines, the intervention for the research participants is expected to address deficits in strength, mobility, balance, and cardiovascular endurance.
Exercise prescription will be provided using the Wellpepper physical therapy exercise prescription mobile app.
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No Intervention: Control
The control group will receive physical therapy as determined by the physical therapist based on clinical practice guidelines and will receive the home exercise program in the traditional way through paper exercise handouts
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exercise adherence
Time Frame: 0, 6, and 12 weeks
|
Mean weekly exercise frequency over 6 and 12 weeks:0-21 with higher scores indicating more adherence.
|
0, 6, and 12 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ShortMAC Physical Function Patient Reported Outcome MeasureRO
Time Frame: 0, 6 and 12 weeks
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12-item assessment of pain and function in people with osteoarthritis: 0-100 scale with higher scores for higher function and less pain
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0, 6 and 12 weeks
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|
2 minute walk test
Time Frame: 0, 6 and 12 weeks
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Functional exercise capacity: Score is in meters/feet with higher distances indicating better exercise capacity
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0, 6 and 12 weeks
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Measure of Intermittent and Constant Osteoarthritis Pain (ICOAP)
Time Frame: 0, 6 and 12 weeks
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Pain measure: Scale range 0-100 with higher scores indicating worse pain
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0, 6 and 12 weeks
|
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Timed Up and Go (TUG) + Dual Task
Time Frame: 0, 6 and 12 weeks
|
Measure of physical function: Score is in seconds with higher scores indicating worse physical function
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0, 6 and 12 weeks
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Dynamic Balance: Four square balance test
Time Frame: 0, 6 and 12 weeks
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Test of dynamic balance: Score is in seconds with lower scores indicating better dynamic balance
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0, 6 and 12 weeks
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Self-efficacy for exercise (SEE) Scale
Time Frame: 0, 6, and 12 weeks
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Self-Efficacy for Exercise Scale: Score range 0-90 with higher score indicating higher self-efficacy for exercise
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0, 6, and 12 weeks
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Nancy Gell, PT, PhD, University of Vermont
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17_0663
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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