BRAVE: Building Resilience and Values Through E-health
Not Applicable
Completed
- Conditions
- Survivorship
- Interventions
- Other: Online survey questionnaire
- Registration Number
- NCT05227599
- Lead Sponsor
- Stanford University
- Brief Summary
The purpose of this study is to determine the feasibility and acceptability of tracking survivors' and their caregivers, stressors, affect, and symptoms using an electronic diary method, in the time period surrounding their routine check- up with their oncologist.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 56
Inclusion Criteria
- 11-25 years old
- previously received a pediatric cancer diagnosis and treatment for such
- completed cancer treatment <5 years ago, in remission
- Own a smart phone or tablet
- are English proficient
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Exclusion Criteria
- no cognitive, motor, or sensory deficits that could preclude completion of study measures.
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Daily Diary Method Cohort Online survey questionnaire Participants will be asked to complete a self-report questionnaire that has been validated to assess daily affect. There are 5 items assessing positive affect (joyful, cheerful, happy, lively, proud) and 5 items assessing negative affect (miserable, mad, afraid, scared sad). The respondent is asked to rate these 10 different feelings on a 5-point Likert scale from 1, "not much or not at all" to 5, "a lot."
- Primary Outcome Measures
Name Time Method Online survey questionnaire 21 days participants will complete a brief online survey every morning and evening within 1 hour of waking and 1 hour of going to sleep
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Stanford University
🇺🇸San Francisco, California, United States