search
Back to results

Cost-utility and Biological Underpinnings of MBSR in Fibromyalgia Syndrome (EUDAIMON)

Primary Purpose

Fibromyalgia Syndrome

Status
Completed
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
MBSR
FibroQol
TAU
Sponsored by
Fundació Sant Joan de Déu
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia Syndrome focused on measuring Fibromyalgia syndrome, Mindfulness (MBSR), Neuroimaging, Cytokines, Randomized Controlled Trial, Cost-effectiveness, Psychoeducation (FibroQol)

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

General Inclusion Criteria:

  • Patients of both genders between 18-65 years old.
  • Verified diagnosis of FMS according to the American College of Rheumatology criteria (ACR 1990).
  • Ability to understand Spanish language.
  • Written informed consent.

General Exclusion Criteria:

  • Participation in other clinical trials
  • Cognitive impairment according to MINI (total score ≤ 24)
  • Receiving psychological treatment during the last or the current year
  • Previous experience with meditation or mind-body therapies.
  • Physical/psychiatric comorbidity that interferes with treatment (any severe medical illness, psychotic symptoms, substance abuse).
  • Not being able to attend to group sessions.
  • Being involved in ongoing litigation relating to the FMS.

Additional Inclusion Criteria for the biomarkers sub-study (90 participants in total):

  • Female gender
  • Right-handed

Additional Exclusion Criteria for the biomarkers sub-study:

  • Neoplastic illnesses (diagnosed from the medical history), infection, cardiopulmonary, vascular or other internal medical conditions
  • Use of oral or local corticosteroids or anti-cytokine therapy
  • Needle-phobia
  • Impossibility of being scanned in MRI (due to agoraphobia, metal implants, pace-marker…)
  • BMI> 36kg/m2 or >110Kg
  • Consuming > 8 caffeine units per day
  • Smoking > 5 cigarettes per day
  • Acute pain not related to the FMS at the day of biomarkers evaluation
  • Being pregnant or breastfeeding.

Sites / Locations

  • Teaching, Research & Innovation Unit - Parc Sanitari Sant Joan de Déu

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Other

Arm Label

Mindfulness-Based Stress Reduction

Psycho-educational Program

Treatment As Usual

Arm Description

Mindfulness-Based Stress Reduction (MBSR) The MBSR consists in eight 2-h group sessions and an all-day mindfulness retreat, and offers intensive and structured training in mindfulness meditation to help patients to relate to their physical and psychological conditions in more accepting and nonjudgmental ways. Participants will be encouraged to engage in home mindfulness practices. Sessions will be lead by 4 MBSR accredited instructors.

Psycho-educational Program (FibroQol) It consists of eight 2-h group sessions including information about FMS (4 sessions) based on a consensus document of the Health Department of Catalonia + autogenic relaxation (4 sessions).

Treatment As Usual.

Outcomes

Primary Outcome Measures

Effectiveness Evaluation: Revised Fibromyalgia Impact Questionnaire (FIQR)
Cost-utility: Client Service Receipt Inventory (CSRI)
Inflammatory markers: pro- and anti-inflammatory cytokines & hs-CRP
EuroQoL questionnaire (EQ-5D-5L)
Structural neuroimaging: Voxel-Based Morphometry (VBM)
Analysis of morphometric changes associated with participation in the three study arms voxel-by-voxel across the brain and in functionally-defined brain regions of interest relating to meta-awareness, body awareness, memory consolidation-reconsolidation, and emotion regulation.
Functional neuroimaging: pulsed continuous arterial spin labeling (pCASL)
Analysis of changes in regional cerebral blood flow representing response to treatment throughout the brain and in a priori-specified network of brain regions postulated to underpin the sensory-discriminative, cognitive-evaluative and affective-motivational aspects of the pain experience.

Secondary Outcome Measures

Hamilton Anxiety and Depression Scale (HADS)
Perceived Stress Scale (PSS-10)
Multidimensional Inventory of Subjective Cognitive Impairment (MISCI)
Pain Catastrophising Scale (PCS)
Fibromyalgia Survey Diagnostic Criteria (FSDC)

Full Information

First Posted
September 23, 2015
Last Updated
October 11, 2019
Sponsor
Fundació Sant Joan de Déu
Collaborators
Carlos III Health Institute, Preventive Services and Health Promotion Research Network, Parc Sanitari Sant Joan de Déu
search

1. Study Identification

Unique Protocol Identification Number
NCT02561416
Brief Title
Cost-utility and Biological Underpinnings of MBSR in Fibromyalgia Syndrome
Acronym
EUDAIMON
Official Title
Cost-utility and Biological Underpinnings of Mindfulness-Based Stress Reduction (MBSR) in Fibromyalgia Syndrome: A Three-arm Randomized, Controlled Trial (EUDAIMON Project)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
January 1, 2016 (Actual)
Primary Completion Date
June 30, 2018 (Actual)
Study Completion Date
December 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fundació Sant Joan de Déu
Collaborators
Carlos III Health Institute, Preventive Services and Health Promotion Research Network, Parc Sanitari Sant Joan de Déu

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Purpose: Fibromyalgia syndrome (FMS) is a disabling condition mainly characterized by chronic widespread pain, disturbed sleep, fatigue, and distress. The estimated overall prevalence of FMS in Europe is 2.9% and it incurs in high personal, social and healthcare costs. Available treatments in FMS are not curative and there is some evidence of positive effects of mindfulness-based stress reduction (MBSR) in patients with chronic pain and FMS. Nevertheless, although promising, the positive findings obtained in previous studies implementing mindfulness-based interventions in patients with FMS have to be interpreted with caution due to important methodological limitations (e.g. absence of randomization, high attrition rates, or small sample sizes). Therefore, further research in larger studies using more adequate methodologies is warranted. Furthermore, little is known about putative neurobiological processes underpinning the effects of mindfulness training in patients with chronic pain. Aims: The aim of this randomized, controlled trial (RCT) is two-fold: firstly, to assess the effectiveness and cost-utility of MBSR added to treatment as usual (TAU); and secondly, to evaluate the effects of the compared interventions on neurobiological parameters. Specifically, MBSR will be compared to an active control which was previously reported as a cost-effective intervention (TAU + FibroQol psycho-educational program; Luciano et al., 2013) and also vs. TAU alone (in a 12-month follow-up RCT). Brain structure and function of pain-relevant areas and levels of inflammation markers (cytokines) will be assessed pre-post interventions in half of the study participants. Methods: Design: RCT with three arms: TAU + MBSR, TAU + FibroQoL and TAU. Sample: 180 adults with FMS according to the ACR 1990 criteria (N=60 for each study arm) will be recruited from from the Parc Sanitari Sant Joan de Déu Rheumatology Service, Sant Boi de Llobregat, Spain. Half of the participants will be randomly selected to participate in the neurobiological pre-post evaluation (N= 30 each group). All patients will be assessed at baseline, post-intervention and 12-month follow-up for clinical variables, prep-post intervention for biomarkers study, and baseline and 12-month follow-up for cost-related variables.
Detailed Description
Detailed description of the study protocol has been published elsewhere (in an open-access journal): http://bmccomplementalternmed.biomedcentral.com/articles/10.1186/s12906-016-1068-2

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia Syndrome
Keywords
Fibromyalgia syndrome, Mindfulness (MBSR), Neuroimaging, Cytokines, Randomized Controlled Trial, Cost-effectiveness, Psychoeducation (FibroQol)

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
225 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mindfulness-Based Stress Reduction
Arm Type
Experimental
Arm Description
Mindfulness-Based Stress Reduction (MBSR) The MBSR consists in eight 2-h group sessions and an all-day mindfulness retreat, and offers intensive and structured training in mindfulness meditation to help patients to relate to their physical and psychological conditions in more accepting and nonjudgmental ways. Participants will be encouraged to engage in home mindfulness practices. Sessions will be lead by 4 MBSR accredited instructors.
Arm Title
Psycho-educational Program
Arm Type
Active Comparator
Arm Description
Psycho-educational Program (FibroQol) It consists of eight 2-h group sessions including information about FMS (4 sessions) based on a consensus document of the Health Department of Catalonia + autogenic relaxation (4 sessions).
Arm Title
Treatment As Usual
Arm Type
Other
Arm Description
Treatment As Usual.
Intervention Type
Behavioral
Intervention Name(s)
MBSR
Intervention Description
Session 1: Recognising the present moment Session 2: Engaging with the breath Session 3: Practice, practice, practice Session 4: Stress and the flow of emotions Session 5: Stress and thoughts: finding another place to stand Session 6: Interpersonal mindfulness / mindful communication. Session 7: Applying mindfulness Session 8: Making mindfulness a part of your life
Intervention Type
Behavioral
Intervention Name(s)
FibroQol
Intervention Description
Session 1: General information. Expectations of the patients. History of the illness. Principal and secondary symptoms in FM. Physiological mechanisms involved in the genesis of pain. Session 2: Relaxation training-I. Session 3: Diagnosis. Pharmacological and non-pharmacological treatments. Prognosis. Current model of health care in Catalonia. Units specialized in the treatment of FM. Session 4: Relaxation training-II. Session 5: Strategies to increase self-esteem and regulate emotions. Pain experience and recurrent invalidation. Social support (family and friends). Session 6: Relaxation training-III Session 7: Benefits of physical exercise in FM. Session 8: Relaxation training-IV.
Intervention Type
Drug
Intervention Name(s)
TAU
Other Intervention Name(s)
Usual care
Intervention Description
In Spain the treatment as usual provided in FMS is mainly pharmacological and adjusted to the symptomatic profile of the patient. Counselling about aerobic exercise adjusted to patients' physical limitations is usually also provided.
Primary Outcome Measure Information:
Title
Effectiveness Evaluation: Revised Fibromyalgia Impact Questionnaire (FIQR)
Time Frame
Change from baseline scores at 12 months
Title
Cost-utility: Client Service Receipt Inventory (CSRI)
Time Frame
Change from baseline scores at 12 months
Title
Inflammatory markers: pro- and anti-inflammatory cytokines & hs-CRP
Time Frame
Change from baseline values at 2 months
Title
EuroQoL questionnaire (EQ-5D-5L)
Time Frame
Change from baseline scores at 12 months
Title
Structural neuroimaging: Voxel-Based Morphometry (VBM)
Description
Analysis of morphometric changes associated with participation in the three study arms voxel-by-voxel across the brain and in functionally-defined brain regions of interest relating to meta-awareness, body awareness, memory consolidation-reconsolidation, and emotion regulation.
Time Frame
Change from baseline brain gray matter concentration at 2 months
Title
Functional neuroimaging: pulsed continuous arterial spin labeling (pCASL)
Description
Analysis of changes in regional cerebral blood flow representing response to treatment throughout the brain and in a priori-specified network of brain regions postulated to underpin the sensory-discriminative, cognitive-evaluative and affective-motivational aspects of the pain experience.
Time Frame
Change from baseline regional cerebral blood flow at 2 months
Secondary Outcome Measure Information:
Title
Hamilton Anxiety and Depression Scale (HADS)
Time Frame
Baseline, 2-month & 12-month follow-up
Title
Perceived Stress Scale (PSS-10)
Time Frame
Baseline, 2-month & 12-month follow-up
Title
Multidimensional Inventory of Subjective Cognitive Impairment (MISCI)
Time Frame
Baseline, 2-month & 12-month follow-up
Title
Pain Catastrophising Scale (PCS)
Time Frame
Baseline, 2-month & 12-month follow-up
Title
Fibromyalgia Survey Diagnostic Criteria (FSDC)
Time Frame
Baseline, 2-month & 12-month follow-up
Other Pre-specified Outcome Measures:
Title
Five Facets Mindfulness Questionnaire (FFMQ)
Description
Process variable
Time Frame
Baseline, 2-month & 12-month follow-up
Title
Self-Compassion Scale (SCS-12)
Description
Process variable
Time Frame
Baseline, 2-month & 12-month follow-up
Title
Psychological Inflexibility in Pain Scale (PIPS)
Description
Process variable
Time Frame
Baseline, 2-month & 12-month follow-up
Title
Checklist - Adverse events of the interventions
Description
Control variable
Time Frame
2-month
Title
Credibility/Expectancy Questionnaire (CEQ)
Description
Control variable
Time Frame
Baseline (MBSR & FibroQol groups)
Title
Mini-Mental State Examination (MMSE)
Description
Screening measure
Time Frame
Baseline
Title
Structured Clinical Interview for DSM Axis I Disorders (SCID-I)
Description
Screening measure
Time Frame
Baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
General Inclusion Criteria: Patients of both genders between 18-65 years old. Verified diagnosis of FMS according to the American College of Rheumatology criteria (ACR 1990). Ability to understand Spanish language. Written informed consent. General Exclusion Criteria: Participation in other clinical trials Cognitive impairment according to MINI (total score ≤ 24) Receiving psychological treatment during the last or the current year Previous experience with meditation or mind-body therapies. Physical/psychiatric comorbidity that interferes with treatment (any severe medical illness, psychotic symptoms, substance abuse). Not being able to attend to group sessions. Being involved in ongoing litigation relating to the FMS. Additional Inclusion Criteria for the biomarkers sub-study (90 participants in total): Female gender Right-handed Additional Exclusion Criteria for the biomarkers sub-study: Neoplastic illnesses (diagnosed from the medical history), infection, cardiopulmonary, vascular or other internal medical conditions Use of oral or local corticosteroids or anti-cytokine therapy Needle-phobia Impossibility of being scanned in MRI (due to agoraphobia, metal implants, pace-marker…) BMI> 36kg/m2 or >110Kg Consuming > 8 caffeine units per day Smoking > 5 cigarettes per day Acute pain not related to the FMS at the day of biomarkers evaluation Being pregnant or breastfeeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan V. Luciano, PhD
Organizational Affiliation
Teaching, Research & Innovation Unit - Parc Sanitari Sant Joan de Déu
Official's Role
Principal Investigator
Facility Information:
Facility Name
Teaching, Research & Innovation Unit - Parc Sanitari Sant Joan de Déu
City
Sant Boi de Llobregat
State/Province
Barcelona
ZIP/Postal Code
08830
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35222735
Citation
Medina S, O'Daly OG, Howard MA, Feliu-Soler A, Luciano JV. Differential Brain Perfusion Changes Following Two Mind-Body Interventions for Fibromyalgia Patients: an Arterial Spin Labelling fMRI Study. Mindfulness (N Y). 2022;13(2):449-461. doi: 10.1007/s12671-021-01806-2. Epub 2022 Jan 5.
Results Reference
derived
PubMed Identifier
31356450
Citation
Perez-Aranda A, Feliu-Soler A, Montero-Marin J, Garcia-Campayo J, Andres-Rodriguez L, Borras X, Rozadilla-Sacanell A, Penarrubia-Maria MT, Angarita-Osorio N, McCracken LM, Luciano JV. A randomized controlled efficacy trial of mindfulness-based stress reduction compared with an active control group and usual care for fibromyalgia: the EUDAIMON study. Pain. 2019 Nov;160(11):2508-2523. doi: 10.1097/j.pain.0000000000001655.
Results Reference
derived
PubMed Identifier
26921267
Citation
Feliu-Soler A, Borras X, Penarrubia-Maria MT, Rozadilla-Sacanell A, D'Amico F, Moss-Morris R, Howard MA, Fayed N, Soriano-Mas C, Puebla-Guedea M, Serrano-Blanco A, Perez-Aranda A, Tuccillo R, Luciano JV. Cost-utility and biological underpinnings of Mindfulness-Based Stress Reduction (MBSR) versus a psychoeducational programme (FibroQoL) for fibromyalgia: a 12-month randomised controlled trial (EUDAIMON study). BMC Complement Altern Med. 2016 Feb 27;16:81. doi: 10.1186/s12906-016-1068-2.
Results Reference
derived

Learn more about this trial

Cost-utility and Biological Underpinnings of MBSR in Fibromyalgia Syndrome

We'll reach out to this number within 24 hrs