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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
University of California, Los Angeles
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Non-Cancer Chronic Pain

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

First Posted
February 5, 2016
Last Updated
December 28, 2017
Sponsor
University of California, Los Angeles
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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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