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Recruiting NCT06098716

NCT06098716 All in the Family: Promoting Family Function Through Physical Activity

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Clinical Trial Summary
NCT ID NCT06098716
Status Recruiting
Phase
Sponsor University of Victoria
Condition Physical Activity
Study Type INTERVENTIONAL
Enrollment 165 participants
Start Date 2024-09-01
Primary Completion 2028-03-30

Eligibility & Interventions

Sex All sexes
Min Age 6 Years
Max Age 12 Years
Study Type INTERVENTIONAL
Interventions
Self RegulationPA Support & Family Social IdentityEducation

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 165 participants in total. It began in 2024-09-01 with a primary completion date of 2028-03-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this trial is to find out whether adding identity-building and self-regulation training to basic healthy-living education helps families with inactive children (ages 6-12) become more cohesive and physically active. The main question it aims to answer is: Does the identity + self-regulation + education program improve family cohesion more than (a) self-regulation + education or (b) education alone? Researchers will compare three groups-identity+self-regulation+education (ID), self-regulation+education (SR), and education-only (ED)-to see which produces the greatest improvements. Participants will: 1. attend three online workshops at baseline plus two booster sessions at 6-week and 3-month with a project coordinator; 2. complete online questionnaires at baseline, 6-week, 3-month, and 6-month; 3. take part in an exit interview at 6 months.

Eligibility Criteria

Inclusion Criteria: 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 Canada. Children that participate in \<60 minutes/day of moderate to vigorous physical activity (MVPA). Exclusion Criteria: If child is meeting the current physical activity guidelines \>=60 minutes a day of moderate to vigorous physical activity per day. If the participant does not pass the Physical Activity Readiness Questionnaire (PARQ) If children's age falls outside the 6-12 year range

Contact & Investigator

Central Contact

Sandy Courtnall

✉ bml@uvic.ca

📞 250 472 5288

Principal Investigator

Ryan Rhodes, PhD

PRINCIPAL INVESTIGATOR

University of Victoria

Frequently Asked Questions

Who can join the NCT06098716 clinical trial?

This trial is open to participants of all sexes, aged 6 Years or older, up to 12 Years, studying Physical Activity. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06098716 currently recruiting?

Yes, NCT06098716 is actively recruiting participants. Contact the research team at bml@uvic.ca for enrollment information.

Where is the NCT06098716 trial being conducted?

This trial is being conducted at Victoria, Canada.

Who is sponsoring the NCT06098716 clinical trial?

NCT06098716 is sponsored by University of Victoria. The principal investigator is Ryan Rhodes, PhD at University of Victoria. The trial plans to enroll 165 participants.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology