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Clinical Trials/NCT01329861
NCT01329861
Completed
Not Applicable

Guided Internet-based Cognitive Behavioural Treatment for Chronic Back Pain Reduces Catastrophizing:a Randomized Controlled Trial

Linkoeping University1 site in 1 country54 target enrollmentJune 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Back Pain Lower Back Chronic
Sponsor
Linkoeping University
Enrollment
54
Locations
1
Primary Endpoint
Coping Strategies Questionnaire - catastrophizing subscale (CSQ)
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

The aim of this study was to investigate whether an Internet-based cognitive behavioural intervention would have an effect on the symptoms of chronic back pain.

Detailed Description

All participants were screened in a live, structured interview before inclusion. It´s a experimental design with a treatment and a control group measured before and after a treatment period.

Registry
clinicaltrials.gov
Start Date
June 2004
End Date
August 2005
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Linkoeping University

Eligibility Criteria

Inclusion Criteria

  • age between 18-65 years
  • access to the Internet
  • having been in contact with a physician
  • back pain of chronic nature
  • in current employment or on short-term sick leave(not longer than 6 months)

Exclusion Criteria

  • wheelchair user
  • surgical treatment planned
  • history of cardiovascular treatment
  • severe depression

Outcomes

Primary Outcomes

Coping Strategies Questionnaire - catastrophizing subscale (CSQ)

Time Frame: Two weeks pre treatment to two weeks post treatment

Change from baseline in the catastrophizing subscale to two weeks post treatment.

Secondary Outcomes

  • Pain and Impairment Relationship Scale (PAIRS)(Change from baseline Two weeks pre treatment to two weeks post treatment.)
  • Multidimensional Pain Inventory (MPI)(Change from baseline Two weeks pre treatment to two weeks post treatment)
  • Hospital Anxiety and Depression Scale(HADS).(Change from baseline Two weeks pre treatment to two weeks post treatment.)
  • Quality of Life Inventory (QOLI)(Change from baseline Two weeks pre treatment to two weeks post treatment.)

Study Sites (1)

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