Using Ecological Momentary Assessment to Develop an Adaptive Psychological Intervention for Young Adults With Chronic Pain
- Conditions
- Chronic Pain
- Registration Number
- NCT06932432
- Lead Sponsor
- Seattle Children's Hospital
- Brief Summary
The goal of this observational study is to determine real-time contextual vulnerabilities associated with pain in young adults to inform ideal treatment targets for a just-in-time adaptive intervention (JITAI). The main question it aims to answer is:
-What contextual factors and vulnerabilities will predict momentary, next-day, and weekly pain severity? 50 young adults, ages 18-25 with a diagnosis of childhood-onset primary chronic pain, will complete 1) baseline questionnaires on REDCap to collect data on sociodemographics, medical history and treatment, psychological health (i.e., current mood symptoms and previous psychiatric conditions/treatment), and pain (e.g., duration, location) and 2) a 28-day EMA via mobile app to collect survey data on dynamic factors.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 50
- ages 18-25
- diagnosis of childhood-onset chronic pain who were seen for an initial evaluation at Seattle Children's Hospital outpatient specialty clinics.
- not fluent in English
- does not have regular access to the internet and access to a smartphone device (to complete EMA questions)
- presence of chronic disease or serious medical illness (e.g., arthritis, cancer, diabetes)
- serious cognitive impairment or developmental disorder (e.g., autism, intellectual disability)
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Momentary Pain intensity Three times a day for 28 days One item from the Brief Pain Inventory will assess momentary pain intensity (yes/no), followed by "How much pain do you feel on average?" (11-point NRS)
Momentary Pain interference Three times a day for 28 days Two items from the Brief Pain Inventory will assess pain interference with enjoyment in life, and general activity. Higher scores indicate more interference.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Seattle Children's Hospital
🇺🇸Seattle, Washington, United States
Seattle Children's Hospital🇺🇸Seattle, Washington, United StatesCaitlin Murray, PhDContact206-884-0147caitlin.murray@seattlechildrens.org