Feasibility of Choose to Move Replacement Ready

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorUniversity of British Columbia

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

Activity coach hired by the Active Aging Society (activity coaches must speak English to participate in the evaluation);

English-speaking older adults (aged >=50 years) who participate in CTM-RR will be invited to participate in the evaluation

Referral partner (People who work in a healthcare setting who refer patients into the program)

Disqualifiers

non-English speaking activity coach

non-English speaking referral partner

Trial design

Design model

Single group

Treatments tested in this trial

  • Choose to Move Replacement Ready

    Behavioral

    As described under study arm description.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Choose to Move Replacement ReadyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Implementation Outcome: Recruitment

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.

Time frame
baseline
2

Implementation Outcome: Retention

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.

Time frame
baseline, 3, 6 months
3

Implementation Outcome: Dose delivered

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).

Time frame
3 months
4

Implementation Outcome: Dose received

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)

Time frame
3 months

Secondary outcomes

1

Change in physical activity

Single-item physical activity questionnaire. Output measure is self-reported number of days engaging in ≥30 minutes of moderate-to-vigorous physical activity in the past week (range 0-7). Higher scores reflect a better outcome (i.e. increased physical activity)

Time frame
baseline, 3, 6 months
2

Change in walking time

International Physical Activity Questionnaire (IPAQ-SF): assesses self-reported weekly minutes of walking (minutes per week)

Time frame
baseline, 3, 6 months
3

Change in sedentary time

International Physical Activity Questionnaire (IPAQ-SF): assesses self-reported weekly minutes of sedentary time

Time frame
baseline, 3, 6 months
4

Change in bone and muscle strengthening activity

Single-item muscle strengthening activity survey. Number of days in past week doing activities that increase bone and muscle strength

Time frame
baseline, 3, 6 months

Other outcomes

1

Acceptability - CTM-RR program

Acceptability of Intervention Measure (AIM). Activity coaches' perception that CTM-RR is agreeable or satisfactory will be assessed by survey (4 items each on a 1-5 Likert scale with 1 being completely disagree and 5 being completely agree).

Time frame
3 months
2

Appropriateness - CTM-RR program

Intervention Appropriateness Measure (IAM). Extent to which CTM-RR fits the needs of the target population will be assessed by survey (4 items each on a 1-5 Likert scale with 1 being completely disagree and 5 being completely agree)

Time frame
3 months
3

Feasibility - CTM-RR program

Feasibility of Intervention Measure (FIM). Activity coaches' perception that CTM-RR is feasible to deliver will be assessed by survey (4 items each on a 1-5 Likert scale with 1 being completely disagree and 5 being completely agree).

Time frame
3 months
4

Reach

Number of individuals participating in CTM-RR programs will be obtained from program records.

Time frame
3 months

Sponsors and contacts

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University of British Columbia

Lead sponsor

Active Aging Society

Collaborator

Specialist Services Committee (Doctors of BC)

Collaborator