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Clinical Trials/NCT01491269
NCT01491269
Completed
Not Applicable

Guided Internet-delivered Cognitive-behavioral Therapy for Former Chronic Pain Patients: Randomised Controlled Trial

Gerhard Andersson1 site in 1 country72 target enrollmentAugust 2009
ConditionsChronic Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
Gerhard Andersson
Enrollment
72
Locations
1
Primary Endpoint
The Coping Strategies Questionnaire (CSQ)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of the present study was to investigate if guided Internet-delivered Cognitive-behavioral Therapy (CBT) would help chronic pain patients who had previously undergone a multidisciplinary treatment but still have residual problems.

Detailed Description

The present study investigates Internet-delivered CBT as a tertiary intervention. This is motivated by the fact that many pain patients relapse after rehabilitation and some may be in need of additional treatment. The persons who fulfills the inclusion criteria undergoes a structured telephone interview. The study is a experimental design with a treatment and an active control group measured before and after a treatment period. The control group were invited to participate in a moderated online discussion forum. Follow up data was collected six months after the treatment.

Registry
clinicaltrials.gov
Start Date
August 2009
End Date
June 2010
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Gerhard Andersson

professor, Linkoeping University

Linkoeping University

Eligibility Criteria

Inclusion Criteria

  • to have been medically investigated (within one year)
  • completed the multidisciplinary rehabilitation program
  • have residual symptoms after the rehabilitation treatment (defined as functional impairment caused by their pain)
  • have Internet access

Exclusion Criteria

  • planned surgery
  • ongoing medical investigation that could impede participation in the study
  • suffering from acute physical or psychological conditions
  • people confined to wheelchairs
  • people not fluent with the Swedish language

Outcomes

Primary Outcomes

The Coping Strategies Questionnaire (CSQ)

Time Frame: One week pre treatment, one week post treatment

The CSQ contains 50 items divided in eight scales that measures different cognitive and behavioral coping strategies. The different coping strategies are: diverting attention, re-interpreting pain sensations, coping self-statements, ignoring sensations, praying and hoping, catastrophizing, increased behavioral activities and pain behavior (Rosenthiel \& Keefe, 1983). Change from baseline in the different subscales pre- and post treatment.

Secondary Outcomes

  • Quality of Life Inventory (QOLI)(One week pre treatment, one week post after treatment)
  • Chronic Pain Acceptance Questionnaire (CPAQ)(One week pre treatment, one week post treatment)
  • Multidimensional Pain Inventory, MPI(One week pre treatment, one week post treatment)
  • Pain and Impairment Relationship Scale (PAIRS)(One week pre treatment, one week post treatment)
  • Hospital Anxiety and Depression Scale, HADS(One week pre treatment, one week post treatment)

Study Sites (1)

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