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Auricular Acupuncture to Facilitate Outpatient Opioid Weaning

A Randomized Controlled Trial of Auricular Acupuncture to Facilitate Outpatient Opioid Weaning

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02882048
Enrollment
16
Registered
2016-08-29
Start date
2016-09-30
Completion date
2019-02-25
Last updated
2019-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Narcotic Addiction

Keywords

Opioid addiction, Opioid weaning

Brief summary

This study is to compare two groups undergoing opioid weaning as ordered by their referring physicians. One group will undergo the standard opioid weaning process and the other group will have the addition of the NADA Protocol to the weaning process.

Detailed description

The NADA (National Acupuncture Detoxification Association) Protocol is a standardized acupuncture technique in which five designated points in the ear are needled (+/-beads/seeds at points for home acupressure therapy in between treatments). The NADA Protocol is indicated for treatment of the following conditions: detoxification, withdrawal, emotional trauma, craving, stress syndromes, relapse prevention, rehabilitation & recovery maintenance. It is also commonly used for PTSD and addiction; however it has not been studied as an adjunct to outpatient opioid weaning protocols for pain. It is cited in the literature as yielding improvements in engagement, retention, decreased cravings, anxiety, and physical symptoms. Given these documented results, it seems feasible the outpatient opioid weaning patient would likely benefit from this procedure.

Interventions

PROCEDURENADA Protocol

NADA Protocol is a standardized acupuncture technique in which five designated points in the ear are needled.

Standard of care medication management defined by an opioid weaning protocol with specific, symptomatic medication regimens.

Sponsors

Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged 18 and older * Referral to the VUMC Interventional Pain Clinic for opioid weaning and discontinuation.

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
Change from baseline in clinical institute narcotic assessment scale (CINA) for withdrawaltime from beginning of opioid withdrawal intervention to opioid cessation(approximately 6 months)

Secondary

MeasureTime frame
Off-opioids ratetime from beginning of opioid withdrawal intervention to opioid cessation(approximately 6 months)
Change from baseline assessment of psychological distress of weaning, assessed using the Hospital Anxiety and Depression Scale (HADS)9 months
Time to cessation of opioidstime from of beginning of opioid withdrawal intervention to opioid cessation (approximately 6 months)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026