Pain Clinical Trial
— NOPAINOfficial title:
Negating Opioid and Pain Actively Through Intervention
NCT number | NCT03306147 |
Other study ID # | 5170244 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 12, 2017 |
Est. completion date | May 17, 2018 |
Verified date | February 2019 |
Source | Loma Linda University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Chronic pain is one of the most prevalent and debilitating medical conditions and opioid analgesics are a commonly prescribed class of medications in the United States. Opioid efficacy has been proven in terms of managing acute and chronic pain; however, opioid overdose deaths, addictions, and diversions have all continued to increase over the years. The purpose of this study is to increase patient engagement in pain management and education, and to decrease opioid use by 10% over the study period. This study will also help present opportunities for future studies to obtain insight regarding the chronic use of opioids.
Status | Completed |
Enrollment | 33 |
Est. completion date | May 17, 2018 |
Est. primary completion date | May 17, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - at least 18 years of age - history of opioid use for 3 or more months or - currently prescribed and are using long-acting or extended release opioids Exclusion Criteria: - substance use - oncology patients - hematology patients |
Country | Name | City | State |
---|---|---|---|
United States | Loma Linda University | Loma Linda | California |
Lead Sponsor | Collaborator |
---|---|
Loma Linda University | Cardinal Health |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decrease in opioid prescription strength | Opioid usage will be measured by changes in prescription strength of morphine milligram equivalents | Change in prescription strength between date of subject enrollment and 90 days after subject enrollment date | |
Secondary | Reduction in pain as evidenced by decrease in opioid daily dose | Subject will keep a daily opioid calendar to track their opioid daily dose | Change in daily opioid use between date of subject enrollment and 90 days after subject enrollment date | |
Secondary | Improvement in quality of life score as measured by the PEG pain screening tool by units on a scale | Survey will be administered by investigators and completed by the patients before and after the interventions | Change in quality of life score as measured by the PEG pain screening tool by units on a scale between date of subject enrollment and 90 days after subject enrollment date |
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