Actively Recruiting

Phase Not Applicable
Age: 11Years +
All Genders
Healthy Volunteers
ID05382975

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

Led by Seattle Children's Hospital · Updated on 2024-06-26

8000

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a trauma-adapted Comprehensive School Physical Activity Program (CSPAP-T) to increase physical activity opportunities in middle schools. This trial focuses on addressing barriers faced by students who have experienced trauma, such as unique needs in physical activity settings and lack of staff training. The study uses a hybrid implementation-effectiveness design over 3 years to assess how trauma-sensitive approaches affect student activity and well-being. The intervention includes providing dedicated staffing support through Americorps members, offering professional development for teachers and staff on trauma-sensitive physical activity, and conducting setting-specific needs assessments and action planning. Schools will transition from control to intervention phases in three randomized waves, with each school participating in a 2-year intervention followed by a year of maintenance assessment. Participants will be assessed up to twice yearly across fall and spring for physical activity using accelerometers, as well as internalizing and externalizing symptoms and resilient psychosocial functioning. Data collection will occur during control, intervention, and maintenance phases, totaling 1800 student assessments across eight schools. The study also explores systems-level factors impacting implementation and sustainability of the program.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 11Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 11 to 14 years (inclusive)
  • Attend one of the participating schools during the study period
  • Teachers or staff aged 18 or older working at one of the participating schools during the study period
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Data Collection

Duration - Up to 1 year before intervention

Participants provide baseline measurements before the intervention starts, including physical activity and psychosocial assessments.

2 visits per year (Fall and Spring) for up to 1 year

Outpatient Treatment

Duration - 2 years

Participants experience the trauma-sensitive physical activity promotion intervention, which includes staffing support, professional development for teachers and staff, and setting-specific needs assessment and action planning.

2 visits per year (Fall and Spring) during the 2-year intervention phase

Post-intervention Follow-up

Duration - 1 year

Participants are observed to assess the sustainability of the intervention effects on physical activity and psychosocial functioning after the active intervention ends.

2 visits per year (Fall and Spring) during the 1-year follow-up phase

Trial Site Locations

Total: 1 location

1

Seattle Children's Research Institute

Seattle, Washington, United States, 98101

Actively Recruiting

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Research Team

K

Kim Garrett, MPH

P

Pooja Tandon, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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