4.4 Article

Self-Guided Online Cognitive Behavioral Strategies for Chemotherapy-Induced Peripheral Neuropathy: A Multicenter, Pilot, Randomized, Wait-List Controlled Trial

Journal

JOURNAL OF PAIN
Volume 19, Issue 4, Pages 382-394

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.jpain.2017.11.009

Keywords

Chronic pain; chemotherapy-induced peripheral neuropathy; cognitive-behavioral therapy; peripheral nervous system disease/chemically induced

Funding

  1. University of Michigan School of Nursing New Investigator Award and Rackham Graduate Student Research Grant
  2. Damon Runyon Cancer Research Foundation [CI-53-10]
  3. National Institute of Arthritis and Musculoskeletal and Skin Diseases/National Institutes of Health [R01-AR050044]
  4. Department of Defense [DAMD 17-00-2-0018]

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The purpose of this pilot, parallel, randomized controlled trial was to examine the efficacy of a self-guided online cognitive and behaviorally-based pain management intervention (Proactive Self-Management Program for Effects of Cancer Treatment [PROSPECT]) to reduce worst pain for individuals with chronic painful chemotherapy-induced peripheral neuropathy (CIPN). Secondary outcomes included average pain, nonpainful CIPN symptom severity, impression of change, and pain interference. Sixty patients with chronic painful CIPN were recruited from 5 outpatient academic and community cancer centers. Patients were randomized in a 1:1 ratio to receive either 8 weeks of PROSPECT or usual care. A 7-day electronic worst pain intensity diary and standardized measures of pain interference, nonpainful CIPN symptom severity, impression of change, and average pain were administered pre/post intervention. Postintervention mean scores were evaluated between groups using analysis of covariance adjusting for baseline. Individuals who received the PROSPECT intervention (n = 19) had significantly greater improvements in worst pain compared with individuals receiving usual care (n = 19; P = .046, d = .58). There were no significant differences in mean scores between groups for the secondary outcomes (n = 42). A larger, adequately powered study testing the PROSPECT intervention is needed to determine if improvements in pain may be sustained, evaluate the effect of the intervention on the secondary outcomes, and identify mediators of pain intensity related improvement. Perspective: This study explores the efficacy of an 8-week online cognitive behavioral pain management intervention for chronic painful CIPN. Intervention use resulted in greater improvements in worst pain than usual care alone. The findings provide preliminary support for the efficacy of a nonpharmacological intervention for chronic painful CIPN. (C) 2017 by the American Pain Society

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