NCT05978336

Brief Summary

The goal of this randomized controlled trial is to investigate the effectiveness of a health-coaching intervention to improve physical activity in older adults with limited mobility when compared to a control, health education group.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
290

participants targeted

Target at P75+ for not_applicable

Timeline
20mo left

Started Sep 2023

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress62%
Sep 2023Dec 2027

First Submitted

Initial submission to the registry

July 28, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

August 7, 2023

Completed
29 days until next milestone

Study Start

First participant enrolled

September 5, 2023

Completed
3.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2027

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2027

Last Updated

January 13, 2026

Status Verified

January 1, 2026

Enrollment Period

3.8 years

First QC Date

July 28, 2023

Last Update Submit

January 10, 2026

Conditions

Keywords

physical activityhealth coachingexerciselimited mobility

Outcome Measures

Primary Outcomes (1)

  • Mobility

    Measured by the Short Physical Performance Battery (SPPB)

    Baseline, 13-weeks, 26-weeks, 52-weeks

Secondary Outcomes (16)

  • Physical activity

    Baseline, 13-weeks, 26-weeks, 52-weeks

  • Self reported physical activity

    Baseline, 13-weeks, 26-weeks, 52-weeks

  • Gait speed

    Baseline, 13- weeks, 26-weeks, 52-weeks

  • Capacity to complete the 400-m walk in ≤ 15 minutes

    Baseline, 13- weeks, 26-weeks, 52-weeks

  • Cognitive function

    Baseline, 26-weeks, 52-weeks

  • +11 more secondary outcomes

Study Arms (2)

Health Coaching (HC)

EXPERIMENTAL

The health coaching program will be delivered by trained and certified kinesiologists utilizing Brief Action Planning (BAP) principals. The BAP behavior change approach utilizes the following 4 techniques: 1) goal-setting; 2 )action planning; 3) self-monitoring; and 4) feedback. Participants will utilize daily physical activity diaries to enable self-monitoring, and BAP coaches will provide feedback on progress toward individualized physical activity goals.

Behavioral: Health Coaching Program

Health Education Program (ED)

ACTIVE COMPARATOR

This program is an attention control group, which consists of general health education. Education sessions will be delivered either by zoom or in person. The education sessions will cover the following topics: 1) falls prevention; 2) sleep; 3) healthy eating; 4) cognitive health; and 5) mental and emotional health.

Behavioral: Health Education Program

Interventions

Participants will begin with a one-hour, group-based, interactive education session on falls prevention delivered either in-person or by Zoom. Following the initial education session, ED participants will receive additional group education sessions (in-person or by Zoom) with the same duration and schedule as the HC program covering a variety of healthy aging topics.

Also known as: ED
Health Education Program (ED)

The HC program will be delivered over 26-weeks. Participants will have an initial hour-long HC session where the BAP coach will conduct a brief physical assessment and work with the participant to establish their physical activity goals and develop a plan. After the initial consult, coaches will conduct 8 x 20-minute phone calls with participants over the 26-week trial decreasing from bi-weekly phone calls in weeks 1-12 to monthly phone calls in weeks 13-26. Participants in the HC group will have an overall goal of increasing their weekly participation in moderate to vigorous physical activity by 50 minutes, via 5-, 7-, or 10-minute bouts of progressive exercises, at a rate of perceived exertion range of 13-14 ("somewhat hard") by week 16. Participants will have access to specific exercise sessions made available by YouTube and/or hardcopy manuals created by the research team.

Also known as: HC
Health Coaching (HC)

Eligibility Criteria

Age70 Years - 89 Years
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • scored ≤ 9/12 on the SPPB
  • are able to complete the 400-m walk in ≤ 15 minutes without sitting or physical assistance from another person or walker (use of cane is acceptable)
  • scored 22/30 or higher on the Mini-Mental State Examination (MMSE)
  • have no significant functional impairment as indicated by a score of 6/8 or higher on the Lawton and Brody Instrumental Activities of Daily Living Scale
  • are able to safely engage in MVPA as indicated by the PAR-Q+ and by the family or study physician as necessary
  • are community-dwelling
  • are able to provide written informed consent.

You may not qualify if:

  • are diagnosed with dementia or stroke
  • self-report engaging in MVPA ≥ 10 minutes per week in the prior 3 months
  • are unable to understand, speak, and read English proficiently

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Vancouver Coastal Health Research Institute Research Pavilion

Vancouver, British Columbia, V5Z 1L8, Canada

RECRUITING

Related Publications (1)

  • Rice J, Li LC, Davis JC, Pahor M, Madden K, Wei N, Wong H, Skelton DA, McCormick S, Falck RS, Barha CK, Rhodes RE, Loomba S, Sadatsafavi M, Liu-Ambrose T. Supporting physical activity for mobility in older adults with mobility limitations (SuPA Mobility): study protocol for a randomized controlled trial. Trials. 2023 Nov 28;24(1):769. doi: 10.1186/s13063-023-07798-9.

MeSH Terms

Conditions

Mobility LimitationMotor Activity

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and SymptomsBehavior

Study Officials

  • Teresa Liu-Ambrose, PhD

    University of British Columbia

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Nathan Wei, B.Sc.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

July 28, 2023

First Posted

August 7, 2023

Study Start

September 5, 2023

Primary Completion (Estimated)

June 30, 2027

Study Completion (Estimated)

December 30, 2027

Last Updated

January 13, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations