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Web-based Cognitive-behavior Therapy (CBT) for Opioid-treated, Chronic Pain Patients With Aberrant Behavior

Web-based CBT for Opioid-treated, Chronic Pain Patients With Aberrant Behavior

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01498510
Acronym
WebCBTPain
Enrollment
110
Registered
2011-12-23
Start date
2012-02-29
Completion date
2015-01-31
Last updated
2017-05-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain

Keywords

chronic pain, cognitive behavior therapy, web-based intervention

Brief summary

The purpose of this study is to develop and evaluate an innovative, web-based self-management intervention for opioid-treated chronic pain patients who display aberrant drug-related behavior.

Detailed description

Within the past decade, there has been increasing recognition of the limitations and risks of opioid therapy for chronic pain, spurred by the U.S.' widespread epidemic of opioid misuse. Within the clinical context, concerns about long-term opioid therapy persist due to limited evidence of efficacy and the occurrence of medication misuse/abuse (termed aberrant drug-related behavior). Psychosocial approaches, particularly self-management strategies such as cognitive-behavior therapy (CBT), have been found to be efficacious for the treatment of chronic pain. However, most chronic pain patients are not exposed to comprehensive psychosocial interventions, due to factors including pain specialty physicians' lack of familiarity with and time to provide behavioral treatments and insufficient payer coverage for these therapies. To address these public health concerns, this study developed, implemented and evaluated an innovative, web-based CBT intervention for the treatment of chronic pain tailored to the specific needs of patients who are prescribed opioids and present with aberrant behavior. The development of this interactive, web-based intervention was informed by iterative feedback from pain experts and chronic pain patients. In a randomized, controlled trial, chronic pain patients receiving opioid therapy at a pain specialty practice were assigned to receive 12 weeks of either treatment-as-usual (TAU; n=55) or treatment-as-usual plus the web-based intervention (Web-CBT; n=55). The trial evaluated the relative effectiveness of these treatments on the primary outcomes of pain severity, pain interference and aberrant opioid-taking behavior, and the secondary outcomes of pain catastrophizing and pain-related Emergency Department visits. Additional analyses explored the impact of the intervention on several supplementary outcomes, such as various categories of activities, psychiatric distress and positive affect, and examined hypothesized mediators of treatment outcome, including quality of life, social support and expectations about the future.

Interventions

BEHAVIORALWeb-based CBT for chronic pain

An interactive, web-based intervention, based on principles of cognitive behavior therapy (CBT), that is designed to train chronic pain patients in self-management skills to reduce pain and aberrant behavior and improve functioning

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Beth Israel Medical Center
CollaboratorOTHER
National Development and Research Institutes, Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* moderate-to-severe pain for at least 3 months (score of 5 or greater on Brief Pain Inventory) * patient at pain treatment program study site * prescribed opioid analgesics * aberrant drug-related behavior within the past 30 days (endorsing 4 or more items on the Current Opioid Misuse Measure)

Exclusion criteria

* primary headache or cancer pain * scheduled for major surgery within the next 6 months * described by physician as likely to die within the next year * plans to move out of the area within the next 3 months * insufficient ability to provide informed consent or insufficient English to participate in consent process, assessments or computer intervention

Design outcomes

Primary

MeasureTime frame
pain severity, as measured by the Multidimensional Pain Inventory (MPI)6 months
pain interference, as measured by the Multidimensional Pain Inventory (MPI)6 months
aberrant drug-related behavior, assessed via the Current Opioid Misuse Measure (COMM)6 months

Secondary

MeasureTime frame
pain catastrophizing, measured by the Pain Catastrophizing Scale (PCS)6 months
Emergency Department visits for pain6 months

Other

MeasureTime frameDescription
General Activities, Social Activities, Activities Away from Home, Household Chores6 monthsactivity sub-scales of the Multidimensional Pain Inventory (MPI)
expectations about the future, assessed by the Future Scale6 months
psychiatric distress, assessed via the SCL-10R6 months
positive affect, assessed by the Positive Affect Negative Affect Scale (PANAS)6 months
quality of life, as measured by the World Health Organization Quality of Life-BREF6 months
social support, assessed by the MOS Social Support Scale6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026