Metabolism, Muscle Function and Psychological Factors in Fibromyalgia
Primary Purpose
Fibromyalgia
Status
Completed
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Mental distress and relaxation test
Glucose tolerance test
Exercise test
Sponsored by
About this trial
This is an interventional other trial for Fibromyalgia
Eligibility Criteria
Inclusion Criteria:
- fibromyalgia diagnosed by the researchers RM or TZ, based on the ACR criteria from 1990
- Finnish as native language
Exclusion Criteria:
- male sex
- muscular or neuromuscular diseases
- diabetes
- heart disease
- generalised atherosclerosis
- untreated hypertension
- neurological or other disease that systematically affects muscles
- a severe psychiatric disorder
- regular consumption of beta-blockers, bronchodilators, or statins
Sites / Locations
- HelsinkiUCH
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Fibromyalgia patients
Healthy controls
Arm Description
All study subjects, both patients and healthy controls, will attend all three interventions: Mental distress and relaxation test, Glucose tolerance test, and Exercise test
All study subjects, both patients and healthy controls, will attend all three interventions: Mental distress and relaxation test, Glucose tolerance test, and Exercise test
Outcomes
Primary Outcome Measures
metabolomics
the difference of value distribution in metabolics panel between groups
metabolomics (physical stress)
the difference of value distribution in metabolics panel between groups
metabolomics (metabolic stress)
the difference of value distribution in metabolics panel between groups
muscle function (raw)
sEMG signal amplitude
muscle function (normalized)
normalized signal amplitude (%sEMGmax)
muscle rest time
time of sEMG signal amplitude < 0.5% sEMGmax
Secondary Outcome Measures
Perceived distress during mental stress vs. relaxation (baseline)
reported distress intensity (NRS)
Perceived distress during mental stress vs. relaxation (relaxation I)
reported distress intensity (NRS)
Perceived distress during mental stress vs. relaxation (mental stress I)
reported distress intensity (NRS)
Perceived distress during mental stress vs. relaxation (relaxation II)
reported distress intensity (NRS)
Perceived distress during mental stress vs. relaxation (mental stress II)
reported distress intensity (NRS)
Perceived distress during mental stress vs. relaxation (relaxation III)
reported distress intensity (NRS)
Pain intensity during mental stress vs. relaxation (baseline)
reported pain intensity (NRS)
Pain intensity during mental stress vs. relaxation (relaxation I)
reported pain intensity (NRS)
Pain intensity during mental stress vs. relaxation (mental stress I)
reported pain intensity (NRS)
Pain intensity during mental stress vs. relaxation (relaxation II)
reported pain intensity (NRS)
Pain intensity during mental stress vs. relaxation (mental stress II)
reported pain intensity (NRS)
Pain intensity during mental stress vs. relaxation (relaxation III)
reported pain intensity (NRS)
heart rate variability
variability of heart beat interval evaluated as root mean square successive difference (RMSSD)
Full Information
NCT ID
NCT03300635
First Posted
September 12, 2017
Last Updated
December 12, 2019
Sponsor
Helsinki University Central Hospital
Collaborators
University of Helsinki
1. Study Identification
Unique Protocol Identification Number
NCT03300635
Brief Title
Metabolism, Muscle Function and Psychological Factors in Fibromyalgia
Official Title
Metaboliset Muutokset ja Lihastoiminta Fibromyalgiassa
Study Type
Interventional
2. Study Status
Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
September 5, 2015 (Actual)
Primary Completion Date
April 10, 2019 (Actual)
Study Completion Date
April 10, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Helsinki University Central Hospital
Collaborators
University of Helsinki
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Fibromyalgia (FM) is a world widely common syndrome, characterized by widespread pain, often accompanied by general fatigue, soreness, and abnormal sensations (like "pins and needles"). The reasons and the mechanisms (pathogenesis) of FM are still poorly understood. Efficacious therapies cannot be developed without understanding the pathophysiological mechanisms of the disease or syndrome.
FM patients suffer from pain and sense of weakness and fatigue in the muscles, and often report difficulty in relaxing their muscles. So far, the studies on muscle activation in fibromyalgia (mostly using surface electromyography) have shown some unusual functioning, a kind of overuse, but the results have been somewhat contradictory.
FM symptoms share some features with small fibre neuropathy, which is a disease or abnormality of small nerve fibres with a diverse aetiology. Recently, several research groups have shown (studying both the electrical function of superficial nerves and nerve endings of skin samples) that up to 50% of the FM patients with severe symptoms have small fibre neuropathy: their small nerves do not function properly and small nerve fibre density in their skin is reduced. However, as this phenomenon is common but not a rule, it might be rather a consequence of some underlying mechanisms of the syndrome, creating even more symptoms.
The aim is to investigate whether there would exist metabolic changes in FM patients that would create pain and lead to functional changes and damage in small nerve fibres. The investigators also aim to explore the muscle function particularly in distressed situations and at rest. The hypothesis is that a towards-overuse-altered function would create unfavourable metabolic changes. Third, the aim is to investigate some psychological factors (such as tendency to get anxious or distressed) to find out, if there is any association between them and muscle function.
The FM patients as well as healthy control subjects will be recruited at Helsinki University Hospital Pain Clinic and from primary care at Vantaa Health Care Centre. The voluntary test subjects will attend
A muscle function examination of 30 minutes with electromyography using surface electrodes, including mentally distressing tasks and relaxing periods. At the same session, the subject will reply to some questionnaires regarding their symptoms and measuring some psychological factors. Actual pain level will be assessed.
A glucose tolerance test, with other blood samples
A bicycle ergometer exercise test of 20 - 30 minutes, with both physiological and chemical (blood samples) recordings. Actual pain level will be assessed as well.
At this stage, 40 patients and 20 healthy control subjects will be recruited.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients and healthy control subjects will attend the same interventions: a) muscle function test (distressing task vs. relaxing) with e.g. psychological questionnaires, b) glucose tolerance test and other blood analyses including metabolomics, and c) bicycle ergometry with physiological measurements and blood analyses including metabolomics.
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
81 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Fibromyalgia patients
Arm Type
Other
Arm Description
All study subjects, both patients and healthy controls, will attend all three interventions: Mental distress and relaxation test, Glucose tolerance test, and Exercise test
Arm Title
Healthy controls
Arm Type
Other
Arm Description
All study subjects, both patients and healthy controls, will attend all three interventions: Mental distress and relaxation test, Glucose tolerance test, and Exercise test
Intervention Type
Other
Intervention Name(s)
Mental distress and relaxation test
Intervention Type
Other
Intervention Name(s)
Glucose tolerance test
Intervention Type
Other
Intervention Name(s)
Exercise test
Primary Outcome Measure Information:
Title
metabolomics
Description
the difference of value distribution in metabolics panel between groups
Time Frame
up to day 3
Title
metabolomics (physical stress)
Description
the difference of value distribution in metabolics panel between groups
Time Frame
Day 3 (at the end of Exercise test)
Title
metabolomics (metabolic stress)
Description
the difference of value distribution in metabolics panel between groups
Time Frame
Day 2 ( at the end of Glucose test)
Title
muscle function (raw)
Description
sEMG signal amplitude
Time Frame
Day 1
Title
muscle function (normalized)
Description
normalized signal amplitude (%sEMGmax)
Time Frame
Day 1
Title
muscle rest time
Description
time of sEMG signal amplitude < 0.5% sEMGmax
Time Frame
Day 1
Secondary Outcome Measure Information:
Title
Perceived distress during mental stress vs. relaxation (baseline)
Description
reported distress intensity (NRS)
Time Frame
Day 1 ( at the beginning of the recording during the Mental distress and relaxation test)
Title
Perceived distress during mental stress vs. relaxation (relaxation I)
Description
reported distress intensity (NRS)
Time Frame
Day 1 (after the first relaxation phase of the Mental distress and relaxation test)
Title
Perceived distress during mental stress vs. relaxation (mental stress I)
Description
reported distress intensity (NRS)
Time Frame
Day 1 (after the first mental stress phase of the Mental distress and relaxation test)
Title
Perceived distress during mental stress vs. relaxation (relaxation II)
Description
reported distress intensity (NRS)
Time Frame
Day 1 (after the second relaxation phase of the Mental distress and relaxation test)
Title
Perceived distress during mental stress vs. relaxation (mental stress II)
Description
reported distress intensity (NRS)
Time Frame
Day 1 (after the second mental stress phase of the Mental distress and relaxation test)
Title
Perceived distress during mental stress vs. relaxation (relaxation III)
Description
reported distress intensity (NRS)
Time Frame
Day 1 ( after the third relaxation phase of the Mental distress and relaxation test)
Title
Pain intensity during mental stress vs. relaxation (baseline)
Description
reported pain intensity (NRS)
Time Frame
Day 1 ( at the beginning of the recording during the Mental distress and relaxation test)
Title
Pain intensity during mental stress vs. relaxation (relaxation I)
Description
reported pain intensity (NRS)
Time Frame
Day 1 ( after the first relaxation phase of the Mental distress and relaxation test)
Title
Pain intensity during mental stress vs. relaxation (mental stress I)
Description
reported pain intensity (NRS)
Time Frame
Day 1 ( after the first mental stress phase of the Mental distress and relaxation test)
Title
Pain intensity during mental stress vs. relaxation (relaxation II)
Description
reported pain intensity (NRS)
Time Frame
Day 1 (after the second relaxation phase of the Mental distress and relaxation test)
Title
Pain intensity during mental stress vs. relaxation (mental stress II)
Description
reported pain intensity (NRS)
Time Frame
Day 1 (after the second mental stress phase of the Mental distress and relaxation test)
Title
Pain intensity during mental stress vs. relaxation (relaxation III)
Description
reported pain intensity (NRS)
Time Frame
Day 1 (after the third relaxation phase of the Mental distress and relaxation test)
Title
heart rate variability
Description
variability of heart beat interval evaluated as root mean square successive difference (RMSSD)
Time Frame
Day 1
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
The Finnish personal ID system includes identification of gender. As most of clinical FM patients are women, we exclude men to create as much homogenity as possible in our sample.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
fibromyalgia diagnosed by the researchers RM or TZ, based on the ACR criteria from 1990
Finnish as native language
Exclusion Criteria:
male sex
muscular or neuromuscular diseases
diabetes
heart disease
generalised atherosclerosis
untreated hypertension
neurological or other disease that systematically affects muscles
a severe psychiatric disorder
regular consumption of beta-blockers, bronchodilators, or statins
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eija A Kalso, MD, PhD
Organizational Affiliation
Helsinki University Hospital and Helsinki University
Official's Role
Study Chair
Facility Information:
Facility Name
HelsinkiUCH
City
Helsinki
Country
Finland
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data are available for only two of the researchers, Ritva Markkula and Teemu Zetterman, who are recruiting the subjects and collecting and coding their personal data to an unidentified mode.
Citations:
PubMed Identifier
35832286
Citation
Zetterman T, Markkula R, Kalso E. Elevated highly sensitive C-reactive protein in fibromyalgia associates with symptom severity. Rheumatol Adv Pract. 2022 Jun 25;6(2):rkac053. doi: 10.1093/rap/rkac053. eCollection 2022.
Results Reference
derived
PubMed Identifier
34797307
Citation
Zetterman T, Markkula R, Kalso E. Glucose tolerance in fibromyalgia. Medicine (Baltimore). 2021 Nov 19;100(46):e27803. doi: 10.1097/MD.0000000000027803.
Results Reference
derived
PubMed Identifier
33583408
Citation
Zetterman T, Markkula R, Partanen JV, Miettinen T, Estlander AM, Kalso E. Muscle activity and acute stress in fibromyalgia. BMC Musculoskelet Disord. 2021 Feb 14;22(1):183. doi: 10.1186/s12891-021-04013-1.
Results Reference
derived
Learn more about this trial
Metabolism, Muscle Function and Psychological Factors in Fibromyalgia
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