Ignite Creation Date:
2024-05-06 @ 10:21 AM
Last Modification Date:
2024-10-26 @ 12:28 PM
Study NCT ID:
NCT03234439
Status:
COMPLETED
Last Update Posted:
2019-01-04
First Post:
2017-07-24
Brief Title:
Digital Tools for Coping With Chronic Pain
Sponsor:
MyStrength Inc
Organization:
MyStrength Inc
Study Overview
Official Title:
Digital Tools for Coping With Chronic Pain
Status:
COMPLETED
Status Verified Date:
2019-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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
Detailed Description:
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 andor 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
1 Do study participants who are randomized to the myStrength intervention arm experience change in their self-reported ability to function outlook on pain andor 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None