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Clinical Trial Summary

While the primary aim is to improve family functioning via child moderate-vigorous physical activity (MVPA) and parent-child co-physical activity (PA), the proposed driver of these outcomes is parental support of child PA. Most theoretical models applied to understand parental support in family interventions have been social cognitive in nature, where intention is considered the proximal antecedent to behavior, it is not surprising that past approaches in family PA promotion center heavily on the antecedents of intention such as attitudes and perceived control. Nevertheless, a low correlation between intention and behavior in parental support of child PA has been demonstrated Thus, there is a need to continue to improve the effectiveness of family-based interventions in ways to sustain initial behavioral changes. Family-based promotion initiatives are also very timely because parents and children represent low activity groups


Clinical Trial Description

The primary objective of this study is to test the efficacy of three Physical Activity (PA) parenting support promotion approaches on key family function outcomes (e.g., cohesion, organization) among parents of children who were not participating in regular PA at baseline of the study. The secondary objectives are to examine whether these approaches: 1) produce differences in child moderate-vigorous intensity PA (MVPA) and parent-child intergenerational PA, and 2) predict PA using the Multi-Process Action Control Framework (MPAC) augmented to include family social PA identity. Primary Question: Does 1) the promotion of a PA parenting identities+self-regulation skills+education (ID) increase family function outcomes (particularly family cohesion, and family organization) compared with 2) promotion of PA parenting self-regulation skills+education (SR), and 3) an education about PA control condition (ED)? Secondary Question: Does 1) the ID condition increase child moderate to vigorous PA (MVPA) and parent-child co-PA compared with 2) the SR condition and 3) the ED condition? Hypothesis: The ID condition will show significantly larger changes in these PA outcomes compared to the two other conditions after six-months (primary end-point). Further, the SR condition will show significantly larger changes in PA outcomes compared to the ED condition after six-months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06098716
Study type Interventional
Source University of Victoria
Contact Sandy Courtnall
Phone 250 472 5288
Email bml@uvic.ca
Status Not yet recruiting
Phase N/A
Start date April 15, 2024
Completion date March 30, 2028

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