OsteoarthritisOsteoarthritis (OA) of the KneeOsteoarthritis, HipTotal Knee Arthroplasty; Total Hip ArthroplastyMobility LimitationSocial Isolation or LonelinessPainImplementation SciencePhysical InactivitySedentary Behaviors
Investigational drug(s) / intervention(s)
Choose to Move Replacement Ready
Choose to Move Replacement Ready: As described under study arm description.
Study summary
Choose to Move (CTM) is a 3-month, choice-based health-promoting program for low active older adults being scaled-up across British Columbia (BC), Canada. Recently, the investigators adapted CTM for the \>14000 people in BC who are on surgical waitlists for total knee replacement or total hip replacement (TKR/THR) for osteoarthritis (OA). The primary goal of this observational study is to learn if the adapted program, Choose to Move Replacement Ready (CTM-RR), is feasible to deliver to people with hip and/or knee osteoarthritis who are on surgical waitlists for TKR/THR.
Participants who enrol in CTM-RR will answer online survey questions about the program and about their physical activity, mobility, pain, function, quality of life, willingness to undergo surgery, overall perception of their joint condition, psychosocial health, self-efficacy, social isolation, loneliness, and sedentary time. CTM-RR activity coaches will also answer online survey questions about the program. CTM-RR participants, activity coaches, and referral partners will also participate in interviews about the program.
Eligibility
Sex
ALL
Min age
50 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
1. Activity coach hired by the Active Aging Society (activity coaches must speak English to participate in the evaluation);
2. English-speaking older adults (aged \>=50 years) who participate in CTM-RR will be invited to participate in the evaluation
3. Referral partner (People who work in a healthcare setting who refer patients into the program)
Exclusion Criteria:
1. non-English speaking activity coach
2. non-English speaking referral partner
Primary outcome measure(s)
Implementation Outcome: Recruitment — baseline Obtained from program records. Proportion of people who attend the program information session, are eligible, and enrol in the program.
Feasibility Target: Enrol 50% of people attending the program information session who are eligible to participate to the program.
Implementation Outcome: Retention — baseline, 3, 6 months Obtained from evaluation records. Proportion of participants who consent to the evaluation who complete each follow-up assessment.
Feasibility target: A minimum of 80% of participants who consented to the evaluation (and are in the pre-operative period) completing each follow-up assessment.
Implementation Outcome: Dose delivered — 3 months Obtained from post-program survey. Proportion of required intervention components (group meetings and one-on-one consultations) delivered by activity coaches.
Feasibility target: Activity coaches delivering 90% of required intervention components (group meetings and one-on-one consultations).
Implementation Outcome: Dose received — 3 months Obtained from post-program survey. Proportion of participants who consent to the evaluation, attending required intervention components (group meetings and one-on-one consultation)
Feasibility target: Participants who consent to the evaluation attending 6 out of 9 (\>60%) of required intervention components (group meetings and one-on-one consultation)
Implementation Outcome: Fidelity (Proportion of participants who adhered to prescribed exercise) — 3 months Obtained from post-program survey. Measures adherence to prescribed frequency, intensity, duration, and type of exercises performed.
80% of participants adhered to all of the following criteria:
* on average, frequency= two sessions per week or greater
* on average, intensity= 7 out of 10 rating of perceived exertion or greater
* on average, duration= 20 minutes or greater
* on average, exercises were completed as prescribed without omission or substitution of prescribed exercises
Adverse events: Number of adverse events — 3 months Obtained from post-program survey. Number of adverse events related to Choose to Move: Replacement Ready that required medical treatment and/or lasted two or more days.
Trial sites (1)
Facility
City
Region
Status
Active Aging Research Team, Robert H. N. Ho Research Centre
Vancouver
British Columbia
Recruiting
More University of British Columbia trials in Canada
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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