Brain Injury Traumatic Mild Clinical Trial
— SMARTOfficial title:
Kids With mTBI Get SMART: Development and Pilot Trial of a Web-Based Self-Monitoring Activity-Restriction and Relaxation Training Program
Verified date | July 2023 |
Source | Children's Hospital Medical Center, Cincinnati |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
SMART is an interactive web-based program that will allow youth with mild traumatic brain injuries (mTBI) to monitor their symptoms and receive education on problem-solving and coping strategies. This study will evaluate the effectiveness of SMART as a means of improving symptom-management, coping skills, and general well-being during recovery from mTBI. Half of participants will receive the SMART intervention, while half will receive usual care.
Status | Completed |
Enrollment | 74 |
Est. completion date | August 31, 2020 |
Est. primary completion date | August 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 11 Years to 18 Years |
Eligibility | Inclusion Criteria: - 11-18 years old - Sustained mTBI within the past week Exclusion Criteria: - Patient and/or family do not speak and read English - Patient and/or family do not have Internet access - Patient experiencing more severe brain injury (Glasgow coma score <13) - Patient with more than one moderate extracranial injury - Patients with non-mTBI reasons for altered mental status - Patients with severe pre-existing neurologic or cognitive disorders or other disorders that may impair ability to participate in the intervention. |
Country | Name | City | State |
---|---|---|---|
United States | Cincinnati Children's Hospital Medical Center | Cincinnati | Ohio |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital Medical Center, Cincinnati | University of Cincinnati |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in quality of life, as measured by the Pediatric Quality of Life Inventory (PedsQL) | The PedsQL includes 23 items measuring physical, emotional, social, and school functioning. | From baseline to 4 weeks post-injury | |
Secondary | Change in coping strategies, as measured by the Coping Strategies Inventory (CSI-S: Short Form) | The CSI-S is a coping styles measure and has been used with other pediatric TBI samples. Adolescents rate how much they agree with 32-statements regarding different ways of coping with difficult situations on a 5-point Likert scale. Responses are then grouped into primary subscales reflecting eight different coping strategies (e.g., problem-solving, problem avoidance, social withdrawal, etc.). | From baseline to 4 weeks post-injury | |
Secondary | Change in self-efficacy for symptom management, as measured by the Self-Efficacy Scale (S-eS) | This 2-item measure will be developed by the research team based on Bandura's self-efficacy theory. Adolescents will rate their level of confidence that they are able to maintain a plan to manage their symptoms each week | From baseline to 4 weeks post-injury | |
Secondary | Change in general functioning, as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) | PROMIS collects data from the adolescent participant and the parent about the impact a condition has on the adolescent's functioning. | From baseline to 4 weeks post-injury | |
Secondary | Change in health and behavioral symptoms, as measured by the Health and Behavior Inventory (HBI) | The HBI is a 20-item questionnaire which includes a variety of cognitive, somatic, emotional, and behavioral symptoms requiring parents and adolescents to rate the frequency of occurrence of each symptom over the past week on a 4-point scale, ranging from "never" to "often." | From baseline to 4 weeks post-injury |
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