Depression Clinical Trial
Official title:
Digital Tools for Coping With Chronic Pain
Chronic pain is becoming increasingly more prevalent worldwide. High rates of co-morbid psychological distress are also commonly found among individuals living with chronic pain. Often requiring a multi-modal treatment approach, a growing body of literature suggests that digital behavioral health interventions and tools may serve as promising complementary options to help individuals cope with the pain.
The research objective is to evaluate the effectiveness of the myStrength product offerings,
namely the chronic pain focus area, on study participants' functional well-being over time.
The research questions to be answered include the following:
1. Do study participants who are randomized to the myStrength intervention arm experience
change in their self-reported ability to function, outlook on pain, and/or perception of
prescription opioids.
2. Do study participants who are randomized to the myStrength intervention arm experience
change in terms of their behavioral health, such as anxiety and depression levels,
during the study period.
The study team hypothesizes that myStrength study participants will achieve a higher level of
functioning and adopt a more positive outlook toward their pain management as compared to the
waitlist control group. Self-assessments will be repeated throughout the study period to
capture the inflection point of change as well as the sustainability of these changes over
time.
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