Survey and Cognitive Behavior Therapy for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis
Not Applicable
Completed
- Conditions
- Chronic Fatigue SyndromeMyalgic EncephalomyelitisFatiguePain
- Interventions
- Behavioral: CBTBehavioral: Control group
- Registration Number
- NCT00920777
- Lead Sponsor
- Norwegian University of Science and Technology
- Brief Summary
The purpose of this study is to analyze income variables in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis, and to analyze the effect of short vs. long Cognitive Behaviour Therapy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 234
Inclusion Criteria
- Patients referred to St.Olav Hospital, Trondheim
- fulfil the FUKUDA criteria for CFS/ME.
Exclusion Criteria
- Pregnant patients
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- FACTORIAL
- Arm && Interventions
Group Intervention Description 8 weeks CBT CBT - 16 weeks CBT CBT - Control group Control group -
- Primary Outcome Measures
Name Time Method Mental and physical function 1 year Mental and physical function, measured by "SF 36". Success criteria are measured by \>10 point improvement of mental and/ or physical function.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
St.Olavs Hospital
🇳🇴Trondheim, Norway