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Clinical Trials/NCT02265029
NCT02265029
Completed
Not Applicable

Evaluation of Spa Therapy in the Treatment of Fibromyalgia : a Randomized, Controlled, Open Multicenter Study

Association Francaise pour la Recherche Thermale5 sites in 1 country220 target enrollmentSeptember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fibromyalgia
Sponsor
Association Francaise pour la Recherche Thermale
Enrollment
220
Locations
5
Primary Endpoint
Handicap in everyday life
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Fibromyalgia is a common health problem that causes widespread pain and tenderness (sensitive to touch). The pain and tenderness tend to come and go, and move about the body. There is no cure for fibromyalgia. Complementary and alternative therapy such as acupuncture, chiropractic and massage therapy, can be useful to manage fibromyalgia symptoms. Many of these treatments have not been well tested in patients with fibromyalgia. Fibromyalgia affect 3 to 4% of the general population and 14 % of patients with rheumatologic disease. Fibromyalgia is most common in women 90 % in many studies. It most often starts in middle adulthood. A chronic evolution occured for Fibromyalgic patients with a major alteration of quality of life.

Thermalgi is a randomized, multicentre, open label trial wich aims to evaluate the effects of spa therapy in rheumatologia on evolution of disability in daily life of patients with fibromyalgia.

Detailed Description

THERMALGI is a controlled, randomized, multicentre, open label trial wich aims to evaluate the effects of spa therapy in rheumatologia on evolution of disability in daily life of patients with fibromyalgia. Patients with fibromyalgia (American College of Rheumatology Criteria) and a FIQ score (Fibromyalgia Impact Questionnaire) \> 39 will be randomized.

Registry
clinicaltrials.gov
Start Date
September 2014
End Date
October 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Association Francaise pour la Recherche Thermale
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • both sexes, more than 18 years old patients
  • available for a spa treatment in rheumatology during 18 days (immediate or late spa) and a follow-up period of 12 months
  • with fibromyalgia ( ACR criteria 2010) for at least 1 year and with a stable treatment for at least 3 months
  • with a FIQ score \> or = 39 (fibromyalgia moderate to severe)
  • voluntary to participate to the study, informed consent form signed after appropriate information
  • affiliation to the social security system or equivalent

Exclusion Criteria

  • contra-indication of spa treatment (cancer in progress, psychiatrics disorders, immunodeficiency)
  • no previous spa treatment in rheumatology within 1 year prior to inclusion
  • substantial variation of the therapeutic coverage in the previous 3 months the inclusion (change of medicinal class, starting up of a réentrainement in the effort or a cognitivio-behavioral technique)
  • subject with an other chronic severe disease (severe asthma, severe cardiac insuffisiancy, respiratory, renal or liver failures, evolutive rheumatic disease, inflammatory colitis...)
  • subject participating to an other clinical study inerventionnal
  • pregnancy, parturient or breast feeding
  • no psychiatric illness or social situation that would preclude study compliance

Outcomes

Primary Outcomes

Handicap in everyday life

Time Frame: 6 months

Decrease of 14% (success rate) of FIQ questionnaire at 6 months compare to baseline

Secondary Outcomes

  • Fatigue(at baseline, 3, 6, 9 and 12 months)
  • Depression(at baseline, 3, 6, 9 and 12 months)
  • Ability to cope(at baseline, 6 and 12 months)
  • Physical activity(at baseline, 3, 6, 9 and 12 months)
  • Pain evolution(at baseline, 3, 6, 9 and 12 months)
  • Quality of life(at baseline, 3, 6, 9 and 12 months)
  • Sleep quality(at baseline, 3, 6, 9 and 12 months)
  • Objective sleep quality(at baseline, 3, and 6 months)
  • Medico economic impact(at baseline, 3, 6, 9 and 12 months)
  • Objective physical activity(at baseline, 3, and 6 months)

Study Sites (5)

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