Mindfulness-Oriented Recovery Enhancement for Chronic Pain Patients Receiving Opioid Therapy

Sponsor
Florida State University (Other)
Overall Status
Completed
CT.gov ID
NCT01505101
Collaborator
National Institute on Drug Abuse (NIDA) (NIH), Fahs Beck Fund for Research and Experimentation (Other)
115
1
2
21
5.5

Study Details

Study Description

Brief Summary

Persons suffering from chronic pain who are treated with long-term opioid therapy are at risk of misusing prescription opioids and developing opioid addiction. Moreover, long-term use of opioids may result in hyperalgesia, which exacerbates opioid craving and consumption. Mindfulness interventions have been shown reduce chronic pain symptoms, addictive processes, and substance use. The investigators hypothesize that relative to a support group control condition, participation in a novel mindfulness-oriented cognitive intervention, Mindfulness-Oriented Recovery Enhancement (MORE), will result in improved well-being and decreased pain, opioid craving, and opioid misuse behaviors among chronic pain patients receiving opioid therapy.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness-Oriented Recovery Enhancement
  • Behavioral: Conventional Support Group (SG)
Phase 1

Detailed Description

Few behavioral treatments target the cognitive-affective mediators of opioid misuse and addiction in chronic pain patients. As such, novel, multimodal interventions are needed to effectively target key mechanisms in the risk chain from chronic pain to opioid misuse and addiction. The secondary aim of this study is to explore possible cognitive, affective, and psychophysiological mediators of intervention effects on pain, opioid craving, opioid misuse behaviors, and well-being.

Study Design

Study Type:
Interventional
Actual Enrollment :
115 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Mindfulness-Oriented Recovery Enhancement for Chronic Pain Patients Receiving Opioid Therapy: Exploration of Cognitive, Affective, and Physiological Mechanisms
Study Start Date :
Oct 1, 2011
Actual Primary Completion Date :
Jul 1, 2013
Actual Study Completion Date :
Jul 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mindfulness-Oriented Recovery Enhancement

Behavioral: Mindfulness-Oriented Recovery Enhancement
MORE is a multimodal, dual-process group intervention involving mindfulness training, cognitive restructuring, and positive emotion induction. MORE consists of eight, weekly, two-hour group sessions led by a trained therapist.

Active Comparator: Conventional Support Group (SG)

Behavioral: Conventional Support Group (SG)
The control arm will participate in a time-matched, conventional SG led by a Master's level therapist, discussing topics pertinent to chronic pain and opioid misuse. The SG format is adapted from the support group detailed in the evidence-based, Matrix Intensive Outpatient Treatment manual. The SG consists of eight, weekly, two-hour sessions.

Outcome Measures

Primary Outcome Measures

  1. Pain severity, pain functional interference [Baseline, immediately following treatment, and at 3 month follow-up]

    Change in pain severity, functional interference, and relief from pain treatments measured on the Brief Pain Inventory-Short Form.

  2. Opioid craving [Baseline, immediately following treatment, and at 3 month follow-up]

    Change in opioid craving as measured by the Obsessive-Compulsive Drug Use Scale and a single-item measure of instantaneous craving.

  3. Opioid misuse behaviors [Baseline, immediately following treatment, and at 3 month follow-up]

    Change in opioid misuse behaviors as measured by the Current Opioid Misuse Measure

  4. Well-being [Baseline, immediately following treatment, and at 3 month follow-up]

    Change in well-being as measured by the WHO-5

Secondary Outcome Measures

  1. Attentional bias [Baseline and immediately following treatment]

    Change in attentional bias as measured by a dot probe task

  2. Psychophysiological cue-reactivity [Baseline and immediately following treatment]

    Change in psychophysiological cue-reactivity

  3. Emotional response inhibition [Baseline and immediately following treatment]

    Change in emotional response inhibition

  4. Pain coping strategies [Baseline, intervention midpoint, and immediately following treatment]

    Change in reinterpretation of pain sensations, catastrophizing, and suppression.

  5. Anhedonia [Baseline and immediately following treatment]

    Change in anhedonia

  6. Fear of pain [Baseline and immediately following treatment]

    Change in fear of pain

  7. Mindfulness [Baseline, intervention midpoint, and immediately following treatment]

    Change in mindfulness measured by the Five-Facet Mindfulness Questionnaire and the Toronto Mindfulness Scale

  8. Positive reappraisal [Baseline and immediately following treatment]

    Change in positive reappraisal

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • chronic pain diagnosis (ICD-9 diagnoses 338.xx)

  • treatment with prescription opioids for > 3 months

Exclusion Criteria:
  • prior mindfulness training

  • persons who are experiencing acute opioid withdrawal

  • suicidal ideation

  • psychosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 FSU College of Social Work Tallahassee Florida United States 32306-2570

Sponsors and Collaborators

  • Florida State University
  • National Institute on Drug Abuse (NIDA)
  • Fahs Beck Fund for Research and Experimentation

Investigators

  • Principal Investigator: Eric L Garland, PhD, Florida State University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Eric Garland, Assistant Professor, Florida State University
ClinicalTrials.gov Identifier:
NCT01505101
Other Study ID Numbers:
  • DA032517-01
  • R03DA032517
First Posted:
Jan 6, 2012
Last Update Posted:
Aug 6, 2014
Last Verified:
Aug 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 6, 2014