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Family-Based Physical Activity Promotion for Child Physical Activity

N/A
Recruiting
Led By Ryan Rhodes, PhD
Research Sponsored by University of Victoria
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 6 weeks, 3 months, and 6 months
Awards & highlights

Study Summary

This trial will explore if creating a family identity around physical activity can increase a child's physical activity levels over 6 months.

Who is the study for?
This trial is for families with at least one child aged 6-12 who does less than 60 minutes of moderate to vigorous exercise daily. Families must live in specified areas of British Columbia and have no restrictions based on income or ethnicity. Children already meeting exercise guidelines or failing the Physical Activity Readiness Questionnaire are excluded.Check my eligibility
What is being tested?
The study tests if creating a family identity focused on physical activity, combined with education and planning, increases children's moderate to vigorous physical activity more than just standard education and planning after six months.See study design
What are the potential side effects?
Since this intervention involves promoting physical activity through social identity formation within the family, there aren't typical medical side effects; however, increased physical activity may lead to muscle soreness or fatigue.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 6 weeks, 3 months, and 6 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 6 weeks, 3 months, and 6 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change from baseline in children's moderate to vigorous physical activity to 6 months
Secondary outcome measures
Body Composition - Height
Body Composition - Percentage Body Fat
Body Composition - Waist Circumference
+13 more

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Identity formation conditionExperimental Treatment1 Intervention
This 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.
Group II: PA education and planning conditionActive Control1 Intervention
This 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.

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Who is running the clinical trial?

Diabetes CanadaOTHER
10 Previous Clinical Trials
959 Total Patients Enrolled
University of VictoriaLead Sponsor
57 Previous Clinical Trials
11,493 Total Patients Enrolled
1 Trials studying Social Identity
73 Patients Enrolled for Social Identity
Leigh Vanderloo, PhDStudy ChairParticipACTION

Media Library

Social Identity Clinical Trial Eligibility Overview. Trial Name: NCT05794789 — N/A
Social Identity Research Study Groups: PA education and planning condition, Identity formation condition
Social Identity Clinical Trial 2023: Social Identity Highlights & Side Effects. Trial Name: NCT05794789 — N/A
Social Identity 2023 Treatment Timeline for Medical Study. Trial Name: NCT05794789 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Does the eligibility criteria for this medical experiment encompass individuals who are under 25 years old?

"In accordance with the study's regulations, the minimum age to participate is 6 and the maximum age allowable is 12."

Answered by AI

Are there any opportunities to partake in this trial?

"To be eligible for this clinical experiment, prospective participants must have a history of physical activity and lie within the age range 6 to 12 years old. The trial is attempting to recruit 148 individuals in total."

Answered by AI

Are there any vacancies still available for this experiment?

"The details hosted on clinicaltrials.gov suggest that this trial is no longer recruiting patients; the study was initially posted March 31st 2023 and last updated March 20th2023. However, there are over one hundred other clinical trials actively looking for candidates at present."

Answered by AI
~99 spots leftby Mar 2026