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NCT00920777 Clinical Trial

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

Pain Clinical Trial

Official title:
A RCT Study on the Effect of Short and Long Cognitive Behaviour Therapy (CBT) in CFS/ME Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00920777
Other study ID # 21592
Secondary ID 215924.2008.2586
Status Completed
Phase N/A
First received
Last updated
Start date May 2009
Est. completion date May 2015

Study information
Verified date June 2020
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Completed
Enrollment 234
Est. completion date May 2015
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 62 Years
Eligibility Inclusion Criteria:

- Patients referred to St.Olav Hospital, Trondheim

- fulfil the FUKUDA criteria for CFS/ME.

Exclusion Criteria:

- Pregnant patients

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• CBT
Individual Cognitive Behavior Therapy during 16 weeks
• CBT
Individual Cognitive Behavior Therapy during 8 weeks
• Control group
Waiting 16 weeks and receiving 8 weeks individual CBT after waiting period.

Locations
Country Name City State
Norway St.Olavs Hospital Trondheim

Sponsors (2)
Lead Sponsor Collaborator
Norwegian University of Science and Technology St. Olavs Hospital

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Rasouli O, Gotaas ME, Stensdotter AK, Skovlund E, Landrø NI, Dåstøl P, Fors EA. Neuropsychological dysfunction in chronic fatigue syndrome and the relation between objective and subjective findings. Neuropsychology. 2019 Jul;33(5):658-669. doi: 10.1037/ne — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Mental and physical function Mental and physical function, measured by "SF 36". Success criteria are measured by >10 point improvement of mental and/ or physical function. 1 year
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