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Clinical Trials/NCT01487473
NCT01487473
Completed
N/A

The Effects of Mindfulness-Based Stress Reduction on Attention and Pain-related Symptoms in Chronic Pain Patients: A Randomized Controlled Trial

York University1 site in 1 country49 target enrollmentDecember 2011
ConditionsPain

Overview

Phase
N/A
Intervention
Not specified
Conditions
Pain
Sponsor
York University
Enrollment
49
Locations
1
Primary Endpoint
Pain disability and Attention
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

The main purpose of this study is to determine the degree to which Mindfulness-Based Stress Reduction, a group-based psychological therapy that includes mindfulness meditation exercises, reduces depression, anxiety, stress, pain intensity, and interference of pain with daily life among adult chronic pain patients.

The second purpose is to examine the role of attention in improving psychological and physical health for chronic pain patients.

Registry
clinicaltrials.gov
Start Date
December 2011
End Date
November 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nicholas Cepeda

Associate Professor

York University

Eligibility Criteria

Inclusion Criteria

  • Adult chronic pain patients who are proficient in English
  • Capable of interacting with others in a group setting
  • Capable of working with a computer

Exclusion Criteria

  • Alcohol or drug abuse (past history is acceptable as long as their situation has been stable for at least 3 months)
  • Psychiatric psychosis (patients who have a past history of schizophrenia are eligible as long as they are currently stable)
  • Current major depressive disorder
  • Current severe social phobia
  • At immediate risk for suicide
  • Cerebral lesions or tumors (unless medically and cognitively stable)
  • Neurological disease
  • Medically unstable
  • Cognitively unstable
  • Previously participated in a mindfulness meditation program

Outcomes

Primary Outcomes

Pain disability and Attention

Time Frame: Baseline, immediately following treatment, and at 3 months follow up

Change in pain disability assessed by the Pain Disability Index (PDI). Change in attention assessed by an adapted version of the Change Blindness Task

Secondary Outcomes

  • Stress(Baseline, immediately following treatment, and at 3 months follow up)
  • Acceptance(Baseline, immediately following treatment, and at 3 months follow up)
  • Pain Intensity(Baseline, immediately following treatment, and at 3 months follow up)
  • Depression(Baseline, immediately following treatment, and at 3 months follow up)
  • Anxiety(Baseline, immediately following treatment, and at 3 months follow up)
  • Mindfulness(Baseline, immediately following treatment, and at 3 months follow up)

Study Sites (1)

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