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
ConditionsBack Pain Lower Back Chronic
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.
Investigators
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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