Mobile Subthreshold Exercise Program for Concussion (M-STEP)

Information

  • Research Project
  • 10259670
  • ApplicationId
    10259670
  • Core Project Number
    R01HD094722
  • Full Project Number
    5R01HD094722-02
  • Serial Number
    094722
  • FOA Number
    PA-18-480
  • Sub Project Id
  • Project Start Date
    9/8/2020 - 3 years ago
  • Project End Date
    8/31/2025 - a year from now
  • Program Officer Name
    MARDEN, SUSAN F
  • Budget Start Date
    9/1/2021 - 2 years ago
  • Budget End Date
    8/31/2022 - a year ago
  • Fiscal Year
    2021
  • Support Year
    02
  • Suffix
  • Award Notice Date
    8/31/2021 - 2 years ago

Mobile Subthreshold Exercise Program for Concussion (M-STEP)

Concussion in youth is increasingly being recognized as a national health concern, affecting more than one million youth each year. As many as 30% of youth with concussion experience persistent and disabling concussive symptoms lasting more than one month, defined as Persistent Post-Concussive Symptoms (PPCS). PPCS interferes with social relationships and adversely impacts physical and academic function. Previous recommendations for treating PPCS focused on cognitive and physical rest, but in 2016 guidelines shifted based on new research suggesting the benefit of rehabilitative exercise. The rationale behind the use of exercise is that gradual increases in the intensity of physical activity facilitates return to full function. Rehabilitative exercise has since become one of the most common approaches to treating youth with PPCS. However, most programs require weekly centralized visits with a concussion specialist, creating barriers to care. To bridge this gap, we developed an mHealth approach to treat PPCS, utilizing physical activity trackers (Fitbits) and weekly video conferences with trained research staff to eliminate the need for frequent clinical visits. We conducted a series of pilot studies with this approach, finding excellent feasibility, acceptability, and evidence for more rapid declines in concussive symptoms compared to controls. We also found preliminary evidence that mechanisms behind this intervention may stem from both physiologic processes due to increased moderate-to-vigorous physical activity (MVPA) and psychologic processes such as reducing fear- avoidance of concussive symptoms. We thus propose a fully powered, randomized controlled trial (RCT) to rigorously examine the ?Mobile Subthreshold Exercise Program? (M-STEP) for youth with PPCS. We will recruit n=250 youth ages 11-18 years with PPCS lasting 1 to 6 months, and randomize them to 6 weeks of either usual care plus M-STEP (intervention) or usual care plus stretching (control). Youth in M-STEP will be coached through gradual increases in intensity and duration of rehabilitative exercise via weekly video conferencing (Zoom) and will use Fitbits to guide their progress. Youth in the stretching group will act as attention controls, with equivalent study contacts. All youth will complete research-grade measures of MVPA using actigraphy and standardized surveys at multiple time points. Youth will be followed for a total of 6 months. We will use mixed effects models to examine differences between experimental groups in the primary outcome, trajectory of concussive symptoms, and the secondary outcome, changes over time in health-related quality of life, on an intention-to-treat basis. The proposed transdisciplinary R01 RCT will provide definitive information regarding the efficacy of M-STEP for youth with PPCS, examine potential mediators including MVPA and fear-avoidance, and explore the impact of biopsychosocial factors (patient sex and parental protective behaviors).

IC Name
EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT
  • Activity
    R01
  • Administering IC
    HD
  • Application Type
    5
  • Direct Cost Amount
    438890
  • Indirect Cost Amount
    202788
  • Total Cost
    641678
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    865
  • Ed Inst. Type
  • Funding ICs
    NICHD:641678\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    BMIO
  • Study Section Name
    Behavioral Medicine, Interventions and Outcomes Study Section
  • Organization Name
    SEATTLE CHILDREN'S HOSPITAL
  • Organization Department
  • Organization DUNS
    048682157
  • Organization City
    SEATTLE
  • Organization State
    WA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    981053901
  • Organization District
    UNITED STATES