This pilot trial will include 30-40 participants with a diagnosis of fibromyalgia. The purpose of the study is to evaluate an internet-based treatment protocol based on cognitive behavioral therapeutic principles. Participants are required to have a previous diagnosis of fibromyalgia before entering into the trial. The treatment will be 10 weeks long and all included participants will be given treatment, i.e. there is no randomization to a comparison group.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
41
10 weeks of internet-based CBT with online therapist contact
Karolinska Institutet, Department of Clinical Neuroscience, Section of psychiatry, Karolinska Hospital Solna R5
Stockholm, Sweden
The Fibromyalgia Impact Questionnaire
Time frame: Once, 1 week before start of treatment
The Fibromyalgia Impact Questionnaire
Time frame: Once, immediately after treatment
The Fibromyalgia Impact Questionnaire
Time frame: Once, 6 months after treatment
Short form 12-item Questionnaire
Time frame: Once, 1 week before start of treatment
Short form 12-item Questionnaire
Time frame: Once, immediately after treatment
Short form 12-item Questionnaire
Time frame: Once, 6 months after treatment
Hospital Anxiety and Depression Scale
Time frame: Once, 1 week before start of treatment
Hospital Anxiety and Depression Scale
Time frame: Once, immediately after treatment
Hospital Anxiety and Depression Scale
Time frame: Once, 6 months after treatment
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