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Physical ActivityNCT05794789

"We Are an Active Family": Promoting Child Physical Activity Through Social Identity Formation in the Family System

A study testing Social Identity in people with Physical Activity and Social Identity, run by University of Victoria at 2 sites in Canada.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The purpose of our study is to explore the effectiveness of physical activity (PA) identity formation in the family system as a promotor of long-term PA. The primary research question is: Does a family identity formation condition (with education+planning) result in increased child moderate- to vigorous-intensity PA… Read more about this study

Who is it for?
Ages 6 to 12 yearsHealthy volunteers can take part
Conditions the study is for
Physical Activity, Social Identity
What is being tested?
Social Identity
Could I receive a placebo?
No, everyone receives an active treatment
How many people
148 participants
Where
2 sitesCanada
Study dates
10 Aug 2023to 31 Mar 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 12 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Participants will be at least one parent with at least one child between the ages of 6 and 12 years.
  • Families (parents and/or guardians and children) residing in Greater Victoria, Nanaimo, Ladysmith, Duncan, Vancouver, Richmond, Surrey, Burnaby, British Columbia.
  • Children that participate in <60 minutes/day of moderate to vigorous physical activity (MVPA)

Who cannot join

  • If child is meeting the current physical activity guidelines >=60 minutes a day of moderate to vigorous physical activity per day.
  • If participant does not pass Physical Activity Readiness Questionnaire (PARQ)

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Evie Streight, MSc. contact

250 472 5288

bml@uvic.ca

Sandy Courtnall contact

bml@uvic.ca

Canada2 sites, 2 recruiting
  • Psychology of Exercise, Health, and Physical Activity (PEHPA) Laboratory, University of British Columbia

    Vancouver, British Columbia, V6T 1Z1

    Mark Beauchamp, PhD, 001 (604) 822 9140, mark.beauchamp@ubc.ca

    Not yet recruiting
  • Behavioural Medicine Lab, University of Victoria

    Victoria, British Columbia, V8P-5C2

    Evie Streight, 250 472 5288, bml@uvic.ca

    Ryan Rhodes, PhD

    Recruiting

Other trials in Canada

About this study

The purpose of our study is to explore the effectiveness of physical activity (PA) identity formation in the family system as a promotor of long-term PA. The primary research question is:

Does a family identity formation condition (with education+planning) result in increased child moderate- to vigorous-intensity PA (MVPA) compared to a standard comparison education and planning condition at six months? Hypothesis: Child MVPA will be higher for the identity formation condition in comparison to the more standard PA education+planning condition at six months.

Read the detailed description

The secondary research questions will include:

  1. Does the identity formation condition improve child health-related fitness outcomes compared to the education and planning condition at six months? Hypothesis: Child health-related fitness will be higher for the identity formation condition in comparison to the education and planning condition.
  2. Can group differences among behavioural, and health-related fitness outcomes be explained through a mediation model? Hypothesis: The covariance of the assigned conditions (identity formation, planning + education) on child MVPA will be explained by parental support, and through parental support identity (i.e., manipulation check). In turn, the covariance between support and health-related outcomes will be explained by MVPA among conditions. In the case of null outcomes for research question #1, the investigators will instead explore a prediction model of these variables rather than a mediation model.
  3. Is there an intergenerational, seasonal, or sex difference across primary outcomes by assigned condition? Hypothesis: Parents in the identity formation condition will show higher physical activity via some activities being performed with their children (as part of social identity) in comparison to the other condition. No differences in child sex or season are hypothesized based on past research.
Being tested
Social Identity
Keywords
Moderate to vigorous physical activity (MVPA), Childhood obesity, Type 2 Diabetes, Identity formation
Medical subject headings
Motor Activity, Social Identification, Pediatric Obesity, Diabetes Mellitus, Type 2

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Social IdentityBehavioural

    This group will receive the same content as the education+planning as well as two additional sessions. This includes short overviews of the benefits of PA as a family, brainstorming how a family can each assist each other in PA, and an activity for developing a family PA action plan. Behavior change techniques such as identity salience, identity similarity, and identity fit and contrast are included in the coaching session include. This will be supplemented by an organization of fun family PA roles for all members (e.g., activity planner, goal setter, supporter, etc.) to instill involvement as well as items (creation of a family PA t-shirt, family PA photos and display, etc.) to instill distinctiveness, which is a central feature of a social identity. Worksheets and discussion will be included. The second session will involve only the parent(s) to focus on parental support identity and the content is based on the behavior change principles of self-identity theory.

Study groups in NCT05794789
Study groupRoleWhat they receive
PA education and planning conditionNo interventionThis group will receive sessions and information-based booklet and series of worksheets that provide a tangible knowledge translation product for the family. The material will consist of Canada's PA guidelines recommending 60 minutes of MVPA a day and a breakdown of ways for the parent to help their child achieve this PA, outlining three main domains of parental support (encouragement, logistical support, and PA together). The material also contains information about the benefits of PA for the child and how to plan for family PA. The material specifically includes a brainstorming exercise for parents where they list physical activities they think their children have found fun in the past. The investigators will provide this material as prompts/suggestions. This list helps create the template for PA planning by contextualizing what the parents would like to do with their kids. An additional two sessions will include education and planning material related to family healthy eating.
Identity formation conditionExperimentalThis group will receive the same content as the education+planning comparison condition but with two additional coaching sessions. The session will include short overviews of the benefits of PA as a family, brainstorming how a family can each assist each other in PA, and an activity for developing a family PA action plan. Behavior change techniques that align with these approaches and are included in the coaching session include identity salience, identity similarity, as well as identity fit and contrast. This will be supplemented by an organization of fun family PA roles for all members (e.g., activity planner, goal setter, supporter, etc.) to instill involvement as well as items (creation of a family PA t-shirt, family PA photos and display, etc.) to instill distinctiveness, which is a central feature of a social identity.
Receives: Behavioral: Social Identity

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from baseline in children's moderate to vigorous physical activity to 6 months

    Children's physical activity will be quantified by accelerometry. Children will wear an accelerometer for a minimum of 6 hours per day for 7 days at baseline, 6 weeks, 3 months, and 6 months.

    Measured: Baseline, 6 weeks, 3 months, and 6 months

Secondary outcomes (16)
  1. Parent-child intergenerational activity via seven-day accelerometry

    Accelerometer model has a Bluetooth proximity detection feature that can determine the presence (e.g., same room in a house, at the park together) or absence of close proximity between two accelerometers. The outcome variable will be average minutes per day parents and children were both engaging in physical activity at the same time while in close proximity.

    Measured: Baseline - 6 months

  2. Parent-child intergenerational activity measured via parent self-report

    For self-reported PA, the the Godin Leisure-Time Exercise Questionnaire will be used.

    Measured: Baseline - 6 months

  3. Body Composition - Weight

    Weight (kg)

    Measured: Baseline - 6 months

  4. Body Composition - Height

    Height (cm)

    Measured: Baseline - 6 months

  5. Body Composition - Waist Circumference

    Waist circumference (cm)

    Measured: Baseline - 6 months

  6. Body Composition - Percentage Body Fat

    Percentage body fat will be measured using a bioelectric impedance scale

    Measured: Baseline - 6 months

  7. Cardiovascular Fitness (ie: predicted maximal aerobic power)

    Will be assessed during a submaximal exercise test called the mCAFT Step Test

    Measured: Baseline - 6 months

  8. Musculoskeletal Fitness

    Measured using grip strength

    Measured: Baseline - 6 months

  9. Musculoskeletal Endurance

    Measured doing curl ups and push ups

    Measured: Baseline - 6 months

  10. Musculoskeletal Power

    Measured doing vertical jump test

    Measured: Baseline - 6 months

  11. Musculoskeletal Flexibility

    Measured doing sit and reach test

    Measured: Baseline - 6 months

  12. The Multi-Process Action Control (MPAC) Constructs - Instrumental Attitude

    Measured by standardized measurement scale - 1-7 Likert-type scale (strongly disagree to strongly agree)

    Measured: Baseline - 6 months

  13. The Multi-Process Action Control (MPAC) Constructs - Affective Judgements

    Measured by standardized measurement scale - 1-7 Likert-type scale (strongly disagree to strongly agree)

    Measured: Baseline - 6 months

  14. The Multi-Process Action Control (MPAC) Constructs - Perceived Capability

    Measured by standardized measurement scale - 1-7 Likert-type scale (strongly disagree to strongly agree)

    Measured: Baseline - 6 months

  15. The Multi-Process Action Control (MPAC) Constructs - Perceived Opportunity

    Measured by standardized measurement scale - 1-7 Likert-type scale (strongly disagree to strongly agree)

    Measured: Baseline - 6 months

  16. Social Identity

    Measured by standardized measurement scale - 1-7 Likert-type scale (strongly disagree to strongly agree)

    Measured: Baseline - 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Apr 2023
  2. Study start10 Aug 2023
  3. Primary completion31 Mar 2026 (estimated)
  4. Study completion31 Mar 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
148 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05794789
Sponsor's protocol ID
23-0022
Status last verified
Mar 2025
First submitted
2 Mar 2023
Last updated
3 Apr 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Streight E, Beauchamp MR, Smith KJ, Blanchard CM, Carson V, Strachan SM, Vanderloo LM, Courtnall S, Rhodes RE. "We are an active family": a randomized trial protocol to evaluate a family-system social identity intervention to promote child physical activity. BMC Public Health. 2024 Sep 27;24(1):2605. doi: 10.1186/s12889-024-20024-8.

    PubMed 39333930

Questions about this trial

What is this clinical trial studying?

A study testing Social Identity in people with Physical Activity and Social Identity, run by University of Victoria at 2 sites in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 3 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Evie Streight, MSc. (250 472 5288, bml@uvic.ca), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from baseline in children's moderate to vigorous physical activity to 6 months (time frame: Baseline, 6 weeks, 3 months, and 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05794789, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Apr 2025.

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