Auricular Acupuncture for Chronic Pain and Insomnia
CompletedNot applicableNCT03503695
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Background: In the U.S. approximately 1.6 million adults use complementary and alternative or integrative medicine therapy for pain and insomnia. However, very few studies have tested the use of auricular acupuncture (AA) using a standard protocol for participants with chronic pain and insomnia. Objective: To assess the feasibility and acceptability of AA and to evaluate the effectiveness of AA on pain severity score, pain interference score, and insomnia over an 8-day study period. Subjects: 45 participants who met the eligibility criteria and signed the consent were randomized to either the AA group (AAG) or the usual care control group (CG) on day 4. Intervention: A standard AA protocol using penetrating semi-permanent acupuncture needles and in-place for up to four days. Main Outcome Measures: Brief Pain Inventory pain severity and interference scores for pain and Insomnia Severity Index (ISI) for insomnia. Results: The use of the standard AA protocol in the AAG led to significant within- and between-group reduction in pain severity and interference scores when compared to the CG. Both groups showed within-group decrease in ISI. However, the AAG showed significant between-group reduction in ISI severity and from moderate to sub-threshold insomnia. Conclusions: AA was found to show effectiveness in the treatment of chronic pain and insomnia. With a heightened focus on the opioid crisis in the U.S., this easy-to-administer protocol can be an option for treatment modality for military beneficiaries with chronic pain and insomnia.
Study details
- Official title
- Auricular Acupuncture for Chronic Pain and Insomnia: a Randomized Clinical Trial
- Conditions
- Interventions
- Device: Sterile acupuncture semi-permanent (ASP) gold needles
- Sponsor
- Landstuhl Regional Medical Center
- Start date
- 2014-11-01
- Primary completion
- 2017-10
- Sex
- All
- Age range
- from 18 Years to 65 Years
- Results posted
- No results posted in this snapshot
- Countries
- Germany
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * military beneficiary - active duty, retiree, or dependents * between the ages of 18 - 65 years * fall under the care of LRMC footprint * self-report of insomnia based on established research criteria * sleep-onset latency (SOL) or wakefulness after sleep onset of ≥30 minutes; * frequency of at least three times a week; * duration of ≥3 months; * with unrestorative or unrefreshing sleep * NRS Pain rating ≥3 (mild to severe level) * pain for ≥3 months * able to read and understand English * for active duty military, an agreement of supervisor Exclusion Criteria: * hypersensitivity or allergy to gold. * pregnancy or plan for future pregnancy during the duration of the study (since the safety of AA in pregnant women has not been established; based on self-report rather than requiring a pregnancy test) * ear trauma or unhealed wounds on the ear * participation in any other research protocol with a device or drugs * piercing or scar tissue in any of the AA point areas * working in jobs with variable hours (e.g., shift work) * acupuncture treatment within the last 3 months * individuals with valvular prosthetics, hemophilia, or currently receiving an anticoagulant.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03503695