CClinicalTrials.gg
CompletedNCT07561008Updated May 1, 2026

Elders Moving Together: A Pilot Study

An interventional study of Exercise Program in Indigenous Older Adult Health and Wellbeing, sponsored by University of Saskatchewan. Completed at 1 site in Canada. Open to participants aged 50 Years and older. Per ClinicalTrials.gov, last updated 2026-05-01.

Sponsored by University of Saskatchewan · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 2 years 7 months after the study started (first participant enrolled Sep 2023, registered Apr 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
50 Years and older
Sex
All
01

Study summary

This pilot study evaluates the feasibility and acceptability of implementing the Saskatchewan Forever in Motion (FIM) group exercise program in a First Nations community in northwestern Saskatchewan. The study examines changes in physical activity, social connectedness, and quality of life among older adults participating in a 12-week community-led exercise program. The project also explores access-related factors that support participation in community-based exercise programs.

Read the detailed description

The Saskatchewan Forever in Motion (FIM) program is an evidence-based group exercise program for older adults that includes walking, gentle resistance band exercises, balance training, and stretching. The program is delivered by trained community members and aims to reduce barriers to physical activity such as cost, transportation, and cultural insensitivity.

This pilot study will implement the FIM program on Saulteaux First Nation, Saskatchewan, Canada. Twenty adults aged 50+ will be recruited. Participants will attend twice-weekly group exercise sessions for 12 weeks. Data collection includes baseline and post-program surveys assessing physical activity (PASE), quality of life (SF-36), and social connectedness (SPS-10), as well as attendance tracking and qualitative sharing circles exploring access-related factors.

Quantitative data will be analyzed for pre-post changes, and qualitative data will undergo inductive thematic analysis. Findings will inform future implementation of culturally safe exercise programs in Indigenous communities.

02

Conditions studied

  • Indigenous Older Adult Health and Wellbeing

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Keywords

  • Indigenous Peoples
  • Health Promotion
  • Exercise
  • Cultural Safety
  • Wellbeing
03

In context

Motor Activity

2,426 studies on the registry are indexed under Motor Activity; 1,161 are open to participants now.

This study's enrollment of 20 is below the median of 60 across 2,118 interventional studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

University of Saskatchewan is the lead sponsor of 237 studies on the registry; 33 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adults aged 50+
  • Band member or resident of Saulteaux First Nation
  • Able to participate in low-intensity exercise
  • Adults under 50 may attend, but priority is given to those 50+

Exclusion criteria

Exclusion Criteria:

  • Uncontrolled cardiovascular, metabolic, pulmonary, or renal conditions as identified by the CSEP PAR-Q+
  • Determined unable to safely participate in group exercise even with support
  • Unable to provide informed consent and no appropriate substitute decision-maker available
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Participant Arm

    All participants are in this single arm of the study, where they receive 12 weeks of twice-weekly exercise programming in their community

    Behavioral: Exercise Program

Interventions

  • BehavioralExercise Program

    Participants will exercise twice weekly in a group exercise program led by community members at a community center on Saulteaux First Nation

06

What researchers measure

Primary outcomes

  1. Feasibility of Program Implementation

    Feasibility assessed through enrollment numbers, weekly attendance, and adherence (percentage of sessions attended per participant).

    Time frame: 12 weeks

Secondary outcomes

  1. Change in Physical Activity (PASE)

    Self-reported physical activity measured using the Physical Activity Scale for the Elderly.

    Time frame: 12 weeks

  2. Change in Quality of Life (SF-36)

    Self-reported quality of life measured using the Short Form-36 questionnaire.

    Time frame: 12 weeks

  3. Change in Social Connectedness (SPS-10)

    Self-reported social connectedness measured using the Social Provision Scale-10.

    Time frame: 12 weeks

  4. Access-Related Factors Supporting Participation

    Qualitative themes from sharing circles and weekly checklists exploring what helped participants access the program.

    Time frame: 12 weeks

07

Study locations

1 site
  • Saulteaux First Nation Health Center
    Saulteaux First Nation, Saskatchewan, Canada
08

References and documents

Individual participant data

Plan to share: No — No - data will be owned by the participating First Nations communities in accordance with Indigenous data sovereignty principles.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07561008
Lead sponsor
University of Saskatchewan
Collaborators
Saskatchewan Health Research Foundation, Saulteaux First Nation, SK
Responsible party
Wendy Verity (PhD Student, University of Saskatchewan) — Principal investigator
First posted
May 1, 2026
Start date
Sep 11, 2023
Primary completion
Dec 21, 2023
Completion
Dec 21, 2023
Last update
May 1, 2026

Study contacts

Anne Leis, PhD
study chair · University of Saskatchewan

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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