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Understanding and Restoring Dopaminergic Function in Fibromyalgia Patients (FIBRODOPA)

Primary Purpose

Fibromyalgia

Status
Not yet recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
Mindfulness oriented recovery enhancement
Sponsored by
University of Fribourg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Fibromyalgia focused on measuring dopamine, reward, F-DOPA, mindfulness

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Fibromyalgia syndrome
  • no psychiatric disorders
  • right handed
  • older than 18 years,

Exclusion Criteria:

  • male sex
  • history of neurological disorders
  • left handed
  • psychiatric disorders
  • current substance or tobacco abuse
  • current and past substance dependence
  • schizophrenia spectrum disorder
  • any other form of chronic pain apart from Fibromyalgia

Sites / Locations

  • University of Fribourg

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

MORE Mindfulness oriented recovery enhancement group

Control

Arm Description

MORE Mindfulness oriented recovery enhancement group

wait-list

Outcomes

Primary Outcome Measures

Dopamine response
Dopamine response measured with 18F-DOPA as percent Bold signal change Range 0.001 +/-0.009 ml g -1 per min

Secondary Outcome Measures

changes in pain and clinical related measures
measured with the brief pain inventory questionnaire (BPI, Cleeland, 1994) Range: 0-40. 0 corresponds to no interference with pain in daily life and 40 corresponds to maximal interference of pain in daily life

Full Information

First Posted
June 19, 2020
Last Updated
January 12, 2021
Sponsor
University of Fribourg
Collaborators
University of Lausanne, University of Zurich, University of Utah
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1. Study Identification

Unique Protocol Identification Number
NCT04451564
Brief Title
Understanding and Restoring Dopaminergic Function in Fibromyalgia Patients
Acronym
FIBRODOPA
Official Title
Understanding and Restoring Dopaminergic Function in Fibromyalgia Patients Using a Mindfulness-based Psychological Intervention: A [18F]-DOPA Positron Emissions Tomography (PET) Study Study Protocol for the FIBRODOPA Study- a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2021 (Anticipated)
Primary Completion Date
January 2023 (Anticipated)
Study Completion Date
January 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Fribourg
Collaborators
University of Lausanne, University of Zurich, University of Utah

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Fibromyalgia (FM) is a very prevalent and debilitating chronic pain disorder that is difficult to treat. Mindfulness-based techniques are regarded as a very promising approach for the treatment of chronic pain and in particular FM. The Mindfulness-Oriented Recovery Enhancement (MORE) intervention, a mindfulness-based group intervention, has shown beneficial effects in opioid-treated chronic pain patients, including reduced pain severity, functional interference, and opioid dosing, by restoring neurophysiological and behavioral responses to reward. First evidence for a hypodopaminergic state and impaired reward processing in FM have been reported. However, little is known about its impact on dopamine (DA) function and in particular with regard to DA responses to monetary reward in FM. The aim of the present study protocol is to evaluate if MORE is able to restore the DA function in FM patients, in particular with regard to the DA responses to reward, and to reduce pain and mood complaints in FM.
Detailed Description
the present study is a multi-center randomized controlled trial (RCT) with 3 time points: before the intervention, after completion of the intervention and 3-months after completion of the intervention. Eighty FM patients will be randomly assigned to either the MORE intervention (N=40) or to a wait-list control group (N=40). Additionally a comparison group of healthy women (N=20) will be enrolled. The MORE intervention consists of eight 2-hour long group sessions administered weekly over a period of 8 weeks. Before and after the intervention, FM participants will undergo [18F] DOPA Positron Emission Tomography (PET) and functional magnetic resonance (MR) imaging while performing a monetary reward task. The primary outcome will be endogeneous DA changes measured with [18F] DOPA PET at baseline, after the intervention (after 8 weeks for control group), and at 3 months' follow-up. Secondary outcomes will be (1) clinical pain measures and FM symptoms using standardized clinical scales 2) functional brain changes 3) measures of negative and positive affect, stress and reward experience in daily life using the Experience Sampling method (ESM) 4) biological measures of stress including cortisol and alpha-amylase. Design: If the findings of this study confirm the effectiveness of MORE in restoring DA function, reducing pain and improving mood symptoms, MORE can be judged to be a promising means to improve quality of life in FM patients. The findings of this trial may inform health care providers about the potential use of the MORE intervention as a possible non-pharmacological intervention for FM.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
dopamine, reward, F-DOPA, mindfulness

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MORE Mindfulness oriented recovery enhancement group
Arm Type
Experimental
Arm Description
MORE Mindfulness oriented recovery enhancement group
Arm Title
Control
Arm Type
No Intervention
Arm Description
wait-list
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness oriented recovery enhancement
Intervention Description
8- week psychological program based on mindfulness techniques
Primary Outcome Measure Information:
Title
Dopamine response
Description
Dopamine response measured with 18F-DOPA as percent Bold signal change Range 0.001 +/-0.009 ml g -1 per min
Time Frame
within the second year
Secondary Outcome Measure Information:
Title
changes in pain and clinical related measures
Description
measured with the brief pain inventory questionnaire (BPI, Cleeland, 1994) Range: 0-40. 0 corresponds to no interference with pain in daily life and 40 corresponds to maximal interference of pain in daily life
Time Frame
within the second year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Fibromyalgia syndrome no psychiatric disorders right handed older than 18 years, Exclusion Criteria: male sex history of neurological disorders left handed psychiatric disorders current substance or tobacco abuse current and past substance dependence schizophrenia spectrum disorder any other form of chronic pain apart from Fibromyalgia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
katharina Ledermann
Phone
+41765330316
Email
katharina.ledermann@unifr.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Maya Burckhard
Email
maya.burkhard@unifr.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chantal o Martin Sölch, PhD
Organizational Affiliation
University of Fribourg
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Fribourg
City
Fribourg
ZIP/Postal Code
1700
Country
Switzerland
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katharina ledermann
Phone
+41765330316
Ext
+41765330316
Email
katharina.ledermann@unifr.ch
First Name & Middle Initial & Last Name & Degree
Chantal martin Sölch
Email
chantal.martinsoelch@unifr.ch

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35078536
Citation
Ledermann K, von Kanel R, Berna C, Sprott H, Burckhardt M, Jenewein J, Garland EL, Martin-Solch C. Understanding and restoring dopaminergic function in fibromyalgia patients using a mindfulness-based psychological intervention: a [18F]-DOPA PET study. Study protocol for the FIBRODOPA study-a randomized controlled trial. Trials. 2021 Dec 1;22(1):864. doi: 10.1186/s13063-021-05798-1.
Results Reference
derived

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Understanding and Restoring Dopaminergic Function in Fibromyalgia Patients

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