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A Comprehensive Trauma-sensitive Approach to Physical Activity Promotion in Schools (CSPAP-T)

Not Applicable
Recruiting
Conditions
Physical Activity
Interventions
Behavioral: CSPAP-T
Registration Number
NCT05382975
Lead Sponsor
Seattle Children's Hospital
Brief Summary

Investigators will conduct a hybrid implementation-effectiveness trial of a trauma-adapted Comprehensive School Physical Activity Program (CSPAP) intervention. A clustered stepped wedge design will be used, with the duration of the trial being 3 years.

Detailed Description

The Comprehensive School Physical Activity Program (CSPAP) is a multi-component approach by which schools use all opportunities for students to be physically active in 5 domains: physical education; physical activity during school; physical activity before and after school; staff involvement; and family and community engagement. Overall, CSPAP-based interventions have had small effect sizes in impacting youth PA, with larger effect sizes seen when more CSPAP domains are included. CSPAP-based interventions are the least effective, and have the most barriers to implementation and sustainability, in school districts that serve a student population that experience intersecting forms of disadvantage and discrimination. Core reasons for this include: (1) youth who have experienced trauma may have unique needs in PA settings, (2) Teachers/staff are not trained to meet the needs of youth who have experienced trauma in PA settings, and (3) staffing constrains the ability of schools to implement new opportunities for PA.

The effectiveness and implementation of a flexible, systems-level intervention to increase opportunities for trauma-sensitive PA in middle schools will be studied. The intervention seeks to support middle schools in increasing opportunities for trauma-sensitive PA practices in all CSPAP domains-addressing two core systems-level barriers to such implementation (staffing and teacher/staff training) and building in flexibility for setting-specific needs assessment and action planning. Core components include (1) provision of a dedicated staff member (via Americorps) to support school PA (via direct staffing and capacity building), (2) setting-specific needs assessment and action planning, and (3) professional development opportunities for teachers, staff, and coaches related to the provision of trauma-sensitive PA.

The study will use a stepped wedge design with a total of 8 middle schools, in which each school will be randomized to start the intervention at different time points. All schools will provide baseline data and will later switch to the intervention phase in random order and in 3 waves. Based on feasibility considerations, 2 schools will switch from control phase to intervention phase in wedge 1, 3 schools will be in wedge 2, and 3 schools will be in wedge 3. Each 2-year intervention phase will be followed by a year when data will be collected to assess sustainability of the intervention. In total, there will be 20 control phase data collections, 24 intervention phase data collections, and 16 data collections during maintenance phase, for a total of 1800 student-assessments (across all schools and all time periods for 20 control and 40 intervention or post-intervention periods). This study will:

1. Assess how intervention exposure is associated with student (accelerometer-measured) PA

2. Assess how intervention exposure is associated with student internalizing and externalizing symptoms and resilient psychosocial function functioning

3. Assess how intervention exposure is associated with change in PA opportunities at the school level

4. Explore systems-level barriers and facilitators to successful intervention implementation and maintenance.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
8000
Inclusion Criteria
  • Age 11-14 (inclusive)
  • Attend one of the participating schools during the study period

Teacher/Staff Inclusion Criteria:

  • Age 18 or older
  • Work at one of the participating schools during the study period
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Wedge 1 includes Schools 1 and 2.CSPAP-T-
Wedge 2 includes Schools 3, 4, and 5.CSPAP-T-
Wedge 3 includes Schools 6, 7, and 8.CSPAP-T-
Primary Outcome Measures
NameTimeMethod
Change in Physical Activity - Accelerometer measured.2 times per year (Fall, Spring) up to 3 years

This is the primary outcome for this study and will be collected from a gender stratified random subset of at least 45 students per school, at each time point. Physical activity will be objectively measured using the ActiGraph GT3X worn at the hip for 7 day periods (x 24 hour wear) at each of the data collection timepoints (i.e., fall and spring of each school year).

Change in Internalizing and Externalizing Symptoms.2 times per year (Fall, Spring) up to 3 years

Mental health symptomatology will be measured using the Strengths and Difficulties Questionnaire (self-report version for 11-16 year olds), a brief behavioral screening questionnaire. Scores will be calculated for internalizing problems (emotional+peer symptoms, 10 items, scale 0-20) and externalizing problems (conduct+hyperactivity symptoms, 10 items, scale 0-20). This will be asked in surveys digitally distributed to all students in the fall and spring of each school year. Higher scores indicate worse outcomes.

Secondary Outcome Measures
NameTimeMethod
Resilient psychosocial functioning2 times per year (Fall, Spring) up to 3 years

Psychological aspects of adolescent resilience will be measured using the 21-item Adolescent Resilience Scale. This three-factor scale measures emotional regulation, positive future orientation, and novelty seeking. This will be asked in surveys digitally distributed to all students in the fall and spring of each school year.

Trial Locations

Locations (1)

Seattle Children's Research Institute

🇺🇸

Seattle, Washington, United States

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