Adapting the HOPE Social Media Intervention to Reduce Prescription Drug Abuse
Primary Purpose
Non-Cancer Chronic Pain
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Harnessing Online Peer Education (HOPE) Social Media Intervention
Sponsored by
About this trial
This is an interventional prevention trial for Non-Cancer Chronic Pain
Eligibility Criteria
Inclusion Criteria:
- (a) UCLA health system patient,
- (b) ≥ 18 years of age,
- (c) on chronic opioid therapy (> 3 and < 12 months) for chronic non-cancer pain as reported by their physician who referred them.
Exclusion Criteria:
° Does not satisfy inclusion criteria
Sites / Locations
- UCLA
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
intervention
control
Arm Description
behavioral intervention
control
Outcomes
Primary Outcome Measures
Reduction in Current Opioid Misuse Measure (COMM) Score
Secondary Outcome Measures
Full Information
NCT ID
NCT02735785
First Posted
February 5, 2016
Last Updated
December 28, 2017
Sponsor
University of California, Los Angeles
1. Study Identification
Unique Protocol Identification Number
NCT02735785
Brief Title
Adapting the HOPE Social Media Intervention to Reduce Prescription Drug Abuse
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2014 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
4. Oversight
5. Study Description
Brief Summary
The Harnessing Online Peer Education (HOPE) intervention combines social media with a psychology-based interventions to change behavior. This intervention is being applied to reduce prescription drug abuse among patients with chronic pain.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Cancer Chronic Pain
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
51 (Actual)
8. Arms, Groups, and Interventions
Arm Title
intervention
Arm Type
Experimental
Arm Description
behavioral intervention
Arm Title
control
Arm Type
No Intervention
Arm Description
control
Intervention Type
Behavioral
Intervention Name(s)
Harnessing Online Peer Education (HOPE) Social Media Intervention
Primary Outcome Measure Information:
Title
Reduction in Current Opioid Misuse Measure (COMM) Score
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
(a) UCLA health system patient,
(b) ≥ 18 years of age,
(c) on chronic opioid therapy (> 3 and < 12 months) for chronic non-cancer pain as reported by their physician who referred them.
Exclusion Criteria:
° Does not satisfy inclusion criteria
Facility Information:
Facility Name
UCLA
City
Los Angeles
State/Province
California
ZIP/Postal Code
90024
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Adapting the HOPE Social Media Intervention to Reduce Prescription Drug Abuse
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