Cognitive Behavioral Therapy Trial in Fibromyalgia ((FIBCOG))

This study has been completed.
Sponsor:
Collaborators:
Uppsala County Council, Sweden
National Social Insurance Board, Sweden
The Swedish Society of Medicine
Reumatikerförbundet
Information provided by:
Uppsala University
ClinicalTrials.gov Identifier:
NCT01004458
First received: October 29, 2009
Last updated: NA
Last verified: October 2009
History: No changes posted
  Purpose

Previous studies have shown that the disorder fibromyalgia often is preceded by long-term stress. Moreover, an association has been shown between stress, pain and co-morbidity in these patients. Cognitive behavioral therapy (CBT) has been shown effective in reducing stress, anxiety and pain in rheumatoid arthritis and fibromyalgia. The purpose of the present trial was to assess whether CBT may reduce pain and other symptoms and increase well-being and general function, affect biological markers for pain and long-term stress, to a larger extent than treatment "as usual".

Forty eight women with verified fibromyalgia were randomly allocated to an early treatment group or a waiting list group. The early treatment group received CBT group treatment during six months. Measurements of outcome and potential outcome affecting variables were made at baseline, after six months and one year after baseline. The waiting list group received the same CBT treatment as the early treatment group after six months on the waiting list.

The design is thus a traditional "waiting list design", allowing a two parallel group comparison during the first six months and a "before-after" analysis in both groups when the treatment was concluded.


Condition Intervention
Fibromyalgia
Behavioral: Cognitive behavioral therapy
Other: Waiting list

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Randomized Clinical Trial of Cognitive Behavioral Therapy in Women With the Fibromyalgia Disorder

Resource links provided by NLM:


Further study details as provided by Uppsala University:

Primary Outcome Measures:
  • Multidimensional Pain Inventory (MPI) score [ Time Frame: At baseline and at 6 and 12 months after baseline ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Type A behavior measures [ Time Frame: At baseline and at 6 and 12 months after baseline ] [ Designated as safety issue: No ]

Enrollment: 48
Study Start Date: January 2001
Study Completion Date: December 2008
Primary Completion Date: December 2003 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Early treatment group
The experimental group receiving CBT
Behavioral: Cognitive behavioral therapy
The treatment, adopted to reduce hostility and stress behavior, was given during group sessions once a week during six months with two follow-up occasions during the next six months
No Intervention: Waiting list group
The waiting list group served as referents during the trial
Other: Waiting list
The group served as referents during the trial and received no intervention other than measurements at the same points in time as the intervention group

Detailed Description:

Long-lasting pain is a common cause for disability. In several studies 30-40% of the adult general population suffer from pain. In this group of subjects the fibromyalgia syndrome (FMS) is common,. This is a well defined disorder with generalized pain, well defined tenderpoints according to the American Collage of Rheumatology (ACR) criteria, and a number of other associated symptoms. About 5-10% of the general female population suffers from fibromyalgia. The disorder is infrequent among men.

The etiology of the condition is unknown. However, a multi-factorial origin is postulated, where some form of stress is a contributing factor. Also neuro-endocrine disturbances have been observed. Cognitive behavioral therapy CBT) is an evidence based efficient treatment method in depression and panic disorder. In open studies it has proved to be an effective stress and pain reducer.

The purpose of the trial was to evaluate the effect of CBT in a group of female FMS patients regarding pain, stress, and well-being (outcome). A purpose was also to study mediating factors, such as biological markers for stress and pain, and psycho-social factors.

The study population consisted of 48 women, 27-62 years of age, living in Östhammar municipality, central Sweden, with a verified FMS according to the 1992 ACR criteria, and no other serious disorder. The were recruited by advertising in the local printed press and meetings with the local rheumatology patient association.

54 subjects were screened for participation. A physical examination was performed, a medical history was taken, blood samples and saliva specimens for biological markers regarding metabolic status, pain and stress were taken, and a questionnaire was filled out. 48 women fulfilled the inclusion criteria and gave informed consent to participation. A randomized block design was used by which the women were randomly allocated to two groups, an early treatment group and a waiting list group.

The early treatment group was subdivided into four treatment groups with six participants in each. The CBT treatment was given by certified therapists and supervised by the chief therapist, an experienced psychologist. Each group had the same therapist throughout the trial. The therapy was given as group sessions once a week for 20 weeks. When the therapy was completed the outcome variables were measured by means of questionnaire, and the same blood and saliva specimens as at baseline were taken. During the next six months two booster CBT sessions were performed. One year after baseline a final follow-up evaluation was made.

The waiting list group served as reference (or control) group to the early treatment group during the first six months from baseline. No CBT therapy was given, but otherwise exactly the same procedure was followed. When the control period was over the waiting list group got their CBT treatment and evaluations following the same protocol as the early treatment group.

The outcome evaluation are based on a number of questionnaire instruments, such as the Multidimensional Pain Inventory (MPI), the Type A behavior instrument (Everyday stress), The Maastricht Questionnaire ("Vital exhaustion"), and the self administered Montgomery Åsberg Depression Rating Scale (MADRS-S) instrument. The blood sampling aimed at analyzing the neuro-peptides substance P, Met-Enkephalin-Arginine-Phenylalanine (MEAP), beta-endorphin, and neuro-peptide Y, in addition to estrogen, testosterone, prolactin and dehydroepiandrosterone (DHEA). The saliva specimens were intended to measure diurnal variation of cortisol. To standardize the hormonal level all evaluations were done in ovulation phase of the menstrual cycle.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Fibromyalgia according to the American College of Rheumatology criteria
  • Women
  • Age 18-65
  • Living in Östhammar municipality, Sweden
  • Swedish speaking

Exclusion Criteria:

  • severe mental disease
  • drug or alcohol abuse
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01004458

Locations
Sweden
Dept of Public Health and Caring Sciences, Family Medicin and Clinical Epidemiology Section
Uppsala, Sweden, SE-75122
Sponsors and Collaborators
Uppsala University
Uppsala County Council, Sweden
National Social Insurance Board, Sweden
The Swedish Society of Medicine
Reumatikerförbundet
Investigators
Principal Investigator: Bo Karlsson, MD Uppsala University
  More Information

Additional Information:
No publications provided

Responsible Party: Bo Karlsson, MD, Uppsala University
ClinicalTrials.gov Identifier: NCT01004458     History of Changes
Other Study ID Numbers: UCC2000
Study First Received: October 29, 2009
Last Updated: October 29, 2009
Health Authority: Sweden: Swedish Research Council

Keywords provided by Uppsala University:
fibromyalgia
cognitive behavioral therapy
women
pain
stress
type A behavior

Additional relevant MeSH terms:
Fibromyalgia
Myofascial Pain Syndromes
Muscular Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Neuromuscular Diseases
Nervous System Diseases

ClinicalTrials.gov processed this record on July 31, 2014