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Mindfulness-oriented recovery enhancement for chronic pain and prescription opioid misuse: results from an early-stage randomized controlled trial.

Journal of consulting and clinical psychology
June 1, 2014
Eric L Garland et al. (6 authors)
Journal ArticleRandomized Controlled TrialResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to evaluate the feasibility and efficacy of Mindfulness-Oriented Recovery Enhancement (MORE) as a treatment for chronic pain and prescription opioid misuse.

Results Summary

MORE participants showed significant reductions in pain severity and interference, decreased stress arousal and desire for opioids, and were more likely to no longer meet criteria for opioid use disorder post-treatment, though some effects were not sustained at follow-up.

Population

Chronic pain patients (N = 115; mean age = 48 ± 14 years; 68% female) with prescription opioid misuse.

Effective Dosage

Not specified

Duration

8 weeks

Interactions

None mentioned

Extracted Claims (7)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Mindfulness-Oriented Recovery Enhancement (MORE)
decrease
pain severity
Chronic pain patients
-
significantly greater reductions
#1
Mindfulness-Oriented Recovery Enhancement (MORE)
decrease
pain interference
Chronic pain patients
-
significantly greater reductions
#2
Mindfulness-Oriented Recovery Enhancement (MORE)
increase
nonreactivity
Chronic pain patients
-
increased
#3
Mindfulness-Oriented Recovery Enhancement (MORE)
increase
reinterpretation of pain sensations
Chronic pain patients
-
increased
#4
Mindfulness-Oriented Recovery Enhancement (MORE)
decrease
stress arousal
Chronic pain patients
-
significantly less
#5
Mindfulness-Oriented Recovery Enhancement (MORE)
decrease
desire for opioids
Chronic pain patients
-
significantly less
#6
Mindfulness-Oriented Recovery Enhancement (MORE)
decrease
opioid use disorder status
Chronic pain patients
-
significantly more likely to no longer meet criteria
#7
Abstract

OBJECTIVE: Opioid pharmacotherapy is now the leading treatment for chronic pain, a problem that affects nearly one third of the U.S. population. Given the dramatic rise in prescription opioid misuse and opioid-related mortality, novel behavioral interventions are needed. The purpose of this study was to conduct an early-stage randomized controlled trial of Mindfulness-Oriented Recovery Enhancement (MORE), a multimodal intervention designed to simultaneously target mechanisms underpinning chronic pain and opioid misuse. METHOD: Chronic pain patients (N = 115; mean age = 48 ± 14 years; 68% female) were randomized to 8 weeks of MORE or a support group (SG). Outcomes were measured at pre- and posttreatment, and at 3-month follow-up. The Brief Pain Inventory was used to assess changes in pain severity and interference. Changes in opioid use disorder status were measured by the Current Opioid Misuse Measure. Desire for opioids, stress, nonreactivity, reinterpretation of pain sensations, and reappraisal were also evaluated. RESULTS: MORE participants reported significantly greater reductions in pain severity (p = .038) and interference (p = .003) than SG participants, which were maintained by 3-month follow-up and mediated by increased nonreactivity and reinterpretation of pain sensations. Compared with SG participants, participants in MORE evidenced significantly less stress arousal (p = .034) and desire for opioids (p = .027), and were significantly more likely to no longer meet criteria for opioid use disorder immediately following treatment (p = .05); however, these effects were not sustained at follow-up. CONCLUSIONS: Findings demonstrate preliminary feasibility and efficacy of MORE as a treatment for co-occurring prescription opioid misuse and chronic pain. (PsycINFO Database Record (c) 2014 APA, all rights reserved).

Medical Subject Headings (MeSH)
AdultAgedAnalgesics, OpioidArousalChronic PainCombined Modality TherapyFeasibility StudiesFemaleHumansMaleMiddle AgedMindfulnessOpioid-Related DisordersTreatment OutcomeUnited StatesVeterans
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality80/10
Citation Metrics
Total Citations235
Citations/Year21.4
Relative Citation Ratio11.10
NIH Percentile98.2%
Research Impact Scores
APT Score0.95
Weight Score1.93
Normalized Score0.70
Related Supplements
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