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Survey and Cognitive Behavior Therapy for Chronic Fatigue Syndrome/Myalgic Encephalomyelitis

Not Applicable
Completed
Conditions
Chronic Fatigue Syndrome
Myalgic Encephalomyelitis
Fatigue
Pain
Interventions
Behavioral: CBT
Behavioral: 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
GroupInterventionDescription
8 weeks CBTCBT-
16 weeks CBTCBT-
Control groupControl group-
Primary Outcome Measures
NameTimeMethod
Mental and physical function1 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
NameTimeMethod

Trial Locations

Locations (1)

St.Olavs Hospital

🇳🇴

Trondheim, Norway

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