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Completed

NCT Number: NCT05497648

Evaluating Impact and Implementation of Choose to Move (Phase 3)

The objectives of this study are to 1) evaluate whether Choose to Move (CTM) improves health outcomes in older adults who participate and 2) assess whether CTM is delivered as planned and what factors support or inhibit delivery at scale.

CTM is a 6 month, choice-based program for low active older adults being scaled-up across British Columbia, Canada. The goals of CTM are to enhance physical activity, mobility and social connectedness in older adults living in British Columbia, Canada.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre for Hip Health and Mobility

Vancouver, British Columbia, V5Z 1M9, Canada

About this study

CTM is a 6 month, choice-based program for low active older adults being scaled-up in phases across British Columbia, Canada. Within CTM (phase 3), trained activity coaches support older adults in three ways. First, in a one-on-one consultation, activity coaches help participants to set goals and create action plans for physical activity tailored to each person's interests and abilities. Older adults can choose to participate in individual or group-based activities. Second, activity coaches facilitate a series of group meetings with small groups of participants. Finally, activity coaches regularly check in with participants to provide ongoing support. Activity coaches and recreation departments across BC are trained and provided with resources to deliver CTM.

Objectives:

  • To assess the impact (effectiveness) of CTM (phase 3) delivered at scale on the physical activity, mobility and social connectedness of older adults (Part I - Impact Evaluation)
  • To assess whether the program was implemented as planned (fidelity) and investigate factors that support or inhibit implementation at scale (Part II - Implementation Evaluation).

Study Design:

We use a hybrid type 2 effectiveness-implementation (Curran et al 2012) pre-post study design to evaluate CTM. We use mixed-methods (quantitative and qualitative) and collect data at 0 (baseline), 3 (mid-intervention), 6 (post-intervention) and 18 (12-months post-intervention) months to assess effectiveness and implementation of CTM.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(older adults):

  • ≥60 years of age,
  • demonstrate readiness for physical activity via the PAR-Q+ questionnaire (Warburton et al 2011), Get Active Questionnaire (Canadian Society for Exercise Physiology 2017) or a letter of recommendation from their physician
  • <150 min/week physical activity
  • English speaking

Exclusion criteria

(older adults):

  • previous participation in CTM

Inclusion criteria

(delivery partners):

  • Activity coaches will be English speaking BCRPA Registered Older Adult Fitness Leaders or Kinesiologists who are delivering CTM at participating centres
  • Recreation Managers and Coordinators affiliated with participating centres delivering CTM
  • Provincial Partners (e.g., individuals/partners who make strategic and/or policy decisions) at partner organizations delivering Choose to Move

Treatment and study plan

Choose to Move

Behavioral

CTM (phase 3) is a 6-month, flexible, evidence- and choice-based program for low active older adults.

CTM includes

  • One-on-One Consultation Participants meet 1-on-1 with their activity coach at the start of the program to set goals and develop an action plan tailored to their abilities, interests and resources. Older adults can choose to participate in individual or group-based activities.
  • Group Meetings Over the first three months, participants will attend five, 1-hour group-based meetings (up to 12 participants total) led by their activity coach. Meetings cover a discussion topic and provide time and space for social connection between participants.
  • Check-ins Over the six month program, activity coaches will provide six brief telephone check-ins (approximately 15 minutes each and once/month) to discuss their Action Plan and ask questions.

Other names: CTM

Primary outcomes

  1. Change in physical activity

    Time frame: 0, 3, 6, 18-months

    The single item physical activity questionnaire will be used to measure physical activity (Milton, Bull & Bauman, 2011). Output variable is self-reported number of days/week ≥30 min PA in the past week.

Secondary outcomes

  1. Change in loneliness

    Time frame: 0, 3, 6, 18-months

    The three-item loneliness scale (Hughes et al., 2004) will be used to assess change in loneliness. Participants rate three aspects of loneliness. The output variable is loneliness score (range 3-9); lower scores indicate lower levels of loneliness.

  2. Change in social isolation

    Time frame: 0, 3, 6, 18-months

    We assessed social isolation using a three-item questionnaire adapted from two questions on social contact frequency (Veroff et al 1981). The output variable is social isolation score (range 0-15); higher scores indicate less social isolation.

  3. Change in physical functioning

    Time frame: 0, 3, 6, 18-months

    Mobility will be assessed with the Physical Functioning Subscale of the 36-Item Short Form Survey (SF-36; Ware et al., 1989). The measure asks participants to rate if their health limits them in performing 10 different activities. The output variable is an average score from 0-100 of physical functioning, where a higher score indicates a more favourable health state.

  4. Change in physical activity (PAAQ)

    Time frame: 0, 3, 6, 18-months

    The Physical Activity Adult Questionnaire will be used to assess physical activity over the previous 7 days (Garriguet et al 2015). Output variable is minutes of PA/week.

  5. Change in health-related quality of life (EQ-5D-5L Profile)

    Time frame: 0, 3, 6, 18-months

    Health status (EQ-5D-5L Profile) will be assessed with the EQ-5D-5L (The EuroQol Group, 1990). Participants report on mobility, self-care, usual activities, pain/discomfort and anxiety/depression on a scale from 1-5 (level of perceived problems) for each item. Responses are used to create a 5-digit number which will be used descriptively.

  6. Change in health-related quality of life (EQ-5D-5L Level Sum Score)

    Time frame: 0, 3, 6, 18-months

    Health status (EQ-5D-5L Level Sum Score) will be assessed with the EQ-5D-5L (The EuroQol Group, 1990). Participants report on mobility, self-care, usual activities, pain/discomfort and anxiety/depression on a scale from 1-5 (level of perceived problems) for each item. The Level Sum Score uses the 5-digit profile to create a numeric score, with scores ranging from 5-25 (lower levels indicate lower levels of perceived problems).

  7. Change in health-related quality of life (EQ-5D-5L Visual Analogue Scale)

    Time frame: 0, 3, 6, 18-months

    health status (EQ-5D-5L Visual Analogue Scale) will be assessed with the EQ-5D-5L (The EuroQol Group, 1990). Participants report on their health on a visual analogue scale from 0 (worst health) to 100 (best health).

  8. Change in mobility limitations

    Time frame: 0, 3, 6, 18-months

    Two items will assess change in a participants' ability to walk a quarter of a mile and up 10 steps (Simonsick et al., 2008). The output variable is self-reported presence of mobility-disability (no/any difficulty walking 400m or climbing one flight of stairs).

  9. Change In sitting time

    Time frame: 0, 3, 6, 18-months

    A five-item questionnaire (Marshall et al., 2010) will be used to assess change in sitting time (hours and minutes) each day in the following domains: (a) while travelling to and from places (e.g., work, shops); (b) while at work; (c) while watching television; (d) while using a computer at home; and (e) at leisure not including watching television (e.g., visiting friends, movies, eating out) on a weekday and a weekend day. The output variables are sitting hours per day across 5 domains

  10. Change in social network

    Time frame: 0, 3, 6, 18-months

    We use a six-item questionnaire (Lubben et al., 2006) to assess social isolation. The output variable is an equally weighted sum (range 0-30).

  11. Change in grip strength (subset)

    Time frame: 0, 3, 6, 18-months

    We assess grip strength using a hand grip dynamometer and standard protocols. We combine the best trial from each side and report the sum as total grip strength.

  12. Change in lower extremity function (subset)

    Time frame: 0, 3, 6, 18-months

    We use the short performance physical battery (SPPB) to assess lower extremity functioning (Guralnik et al 1994). The output variable is an equally weighted sum of 3 subscores (range 0-12); higher scores represent better performance.

  13. Change in physical activity (CHAMPS)

    Time frame: 0, 3, 6, 18-months

    We use the CHAMPS questionnaire (Stewart et al 2001) to assess weekly frequency and duration of a variety of physical activities and use the CHAMPS scoring algorithms to calculate energy expenditure (kcal/week) and frequency (times/week).

Other outcomes

  1. Reach-individual

    Time frame: 6 months

    The number of participants engaged in the intervention is obtained from program records.

  2. Reach-organizational

    Time frame: 6 months

    The number of organizations and activity coaches delivering the intervention is obtained from program records.

  3. Dose

    Time frame: 6 months

    The amount of intervention delivered is assessed via survey (designed in house)

  4. Fidelity

    Time frame: 6 months

    Fidelity to planned delivery is assessed via survey (designed in house) and interview/focus group.

  5. Participant responsiveness

    Time frame: 6 months

    We assess program satisfaction via participant survey (designed in house) and interviews.

  6. Adaptation

    Time frame: 6 months

    We assess adaptation of the intervention and its delivery via survey (designed in house) and interview/focus groups

  7. Contextual factors influencing implementation

    Time frame: 6 months

    We use surveys (designed in house) and interviews/focus groups to describe how community level factors, provider characteristics, characteristics of the innovation, the prevention delivery system, organizational capacity and the prevention support system influenced program delivery.

  8. Cost

    Time frame: 6 months

    We use a cost capture template to record program delivery costs.

Sponsors and collaborators

Lead sponsor

University of British Columbia

Other

Collaborators

  • Active Aging Society
  • Canadian Institutes of Health Research (CIHR)

Registry information

Official study title

Choose to Move: Impact and Implementation Evaluation of a Program to Enhance Older Adult Physical Activity, Mobility and Health

Acronym: CTM

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Aug 11, 2022
Registry last updated
Aug 22, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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