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Anti-inflammatory Nutritional Intervention in Patients With Fibromyalgia

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Anti-inflammatory and low FODMAPs diet
General healthy eating
Sponsored by
Universidade do Porto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Fibromyalgia focused on measuring Antiinflammatory diet, Low FODMAPs diet, Gluten, casein, sugar and processed-foods free diet, Nutrition

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of FM performed by the physician, according to the Rome III criteria of the American College of Rheumatology, revised in 2010;
  • Ability to read and sign the Informed Consent;
  • Stable dose therapy within 4 weeks before study start.

Exclusion Criteria:

  • Patients with pathologies that prevent the follow-up of the given dietary protocol;
  • Patients currently undergoing lactation or pregnancy;
  • Prior or current clinical history of abuse of drug or other substances;
  • Change of therapy during the intervention period;
  • Presence of other inflammatory diseases;
  • Uncontrolled medical conditions (eg. Diabetes Mellitus, decompensated heart disease, renal failure, neoplastic diseases, liver diseases).

Sites / Locations

  • Instituto Português de Reumatologia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Anti-inflammatory and low FODMAPs diet

Control

Arm Description

The anti-inflammatory diet is characterized by the exclusion of potential inflammatory foods, such as gluten, dairy and processed food, for three months. During the first month, a low FODMAPs diet will be implemented, followed by the reintroduction of all fruits and vegetables over a consecutive period of 2 months. Additionally, some potentially anti-inflammatory foods will be promoted: Omega-3 through specific fish (tuna fish, salmon, sardine, horse mackerel) and nuts, antioxidant rich foods, such as fruit and vegetables, and the maintenance of glycemic index.

Dietary counselling based on general recommendations for healthy eating according to the World Health Organization

Outcomes

Primary Outcome Measures

Change in pain, accessed by Visual Analogue Pain Scale
Accessed by Visual Analogue Pain Scale (1 question about pain intensity over the last month, score: 0-10, with 0 = a total pain relief and 10=the greatest pain ever felt).
Change in pain, accessed by Brief Pain Inventory
Accessed by Brief Pain Inventory (12 questions about pain severity and pain interference; presented with 0-10 scales, with 0=no interference and 10=interferes completely; scale range from 0 to 120 - higher range represent a worst result).
Change in quality of life accessed by Revised Fibromyalgia Impact Questionnaire
Accessed by Revised Fibromyalgia Impact Questionnaire (20 questions about physical functioning (score 0-3, with 0 = optimal and 3 = worst), and about work difficulty, pain, fatigue, morning tiredness, stiffness, anxiety and depression (score 1-10, with 1 = optimal and 10 = worst; scale range from 0 to 117 - higher range represent a worst result).
Change in quality of life accessed by Short-form 36
Accessed by Short-form 36 (36 questions related to the last month, distributed in 8 dimensions: physical function (Score 1-3, with 1 = very limited and 3 = not limited), physical performance, pain, general health, vitality, social function, emotional performance and mental health (score 1-5, with 1 = bad and 5-optimal); scale range from 36 to 142 - higher range represent a worst result).
Change in inflammatory parameters accessed by serum C-reactive protein measurement
Measurement of serum C-reactive protein (mg/L).
Change in inflammatory parameters accessed by serum erythrocyte sedimentation rate measurement
Measurement of serum erythrocyte sedimentation rate (mm/h).
Change in inflammatory parameters accessed by serum interleukin-8 measurement
Measurement of serum and interleukin-8 (pg/mL).

Secondary Outcome Measures

Change in fatigue accessed by Fatigue Severity Survey
Accessed by 1 questionnaire: Fatigue Severity Survey (7 questions with scale from 1 to 7, with 1 = fully disagree and 7 = fully agree; scale range from 7 to 49 - higher range represent a worst result).
Change in gastrointestinal symptoms accessed by Visual Analog Scale from a list of common gastrointestinal symptoms
Accessed by questionnaire: Visual Analog Scale from a list of common gastrointestinal symptoms (10 questions about gastrointestinal discomfort over the last month, score: 0-10, with 0 = none and 10 = a big discomfort; scale range from 0 to 100 - higher range represent a worst result).
Change in quality of sleep accessed by Pittsburgh Sleep Quality Index
Accessed by 1 questionnaire: Pittsburgh Sleep Quality Index (18 questions with a scale from 1 to 4, with 1=no sleep disturbance and 4=to much sleep disturbance; scale range from 18 to 72 - higher range represent a worst result).
Change in weight
Measurement of weight in Kilograms.
Change in waist circumference
Measurement of waist circumference in centimeters.
Change in body fat mass
Measurement by bio-impedance of body fat mass in percentage.

Full Information

First Posted
June 4, 2019
Last Updated
November 12, 2021
Sponsor
Universidade do Porto
Collaborators
Portuguese Institute of Rheumatology, Centro de Investigação Interdisciplinar Egas Moniz
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1. Study Identification

Unique Protocol Identification Number
NCT04007705
Brief Title
Anti-inflammatory Nutritional Intervention in Patients With Fibromyalgia
Official Title
Effects of an Anti-inflammatory Nutritional Intervention in Disease Assessment Parameters, Inflammatory Markers, and Quality of Life of Patients With Fibromyalgia
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Completed
Study Start Date
April 9, 2019 (Actual)
Primary Completion Date
June 4, 2020 (Actual)
Study Completion Date
June 4, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universidade do Porto
Collaborators
Portuguese Institute of Rheumatology, Centro de Investigação Interdisciplinar Egas Moniz

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
This is a randomized clinical trial, aimed to analyse the effects of a potentially anti-inflammatory nutritional intervention in disease assessment parameters, inflammatory markers, and quality of life of Fibromyalgia patients. Patients in the intervention group will adopt an anti-inflammatory diet and a diet with a low ingestion of fermentable oligo-, di- and monosaccharides, and polyols (FODMAPs), for a 3 months period. Group control will adopt a diet based on general recommendations for healthy eating in accordance with the World Health Organization.
Detailed Description
The presence of low grade intestinal inflammation has been reported in Fibromyalgia (FM) patients. Other studies associate the persistence of symptoms described in FM to possible alterations of the intestinal microbiota composition, i.e. dysbiosis, with consequent existence of Small Intestinal Bacterial Overgrowth (SIBO). A sample of 100 female patients diagnosed with FM, followed-up at Portuguese Rheumathology Institute in Lisbon, will be distributed randomly in two groups. Group 1 will adopt an anti-inflammatory diet, which is characterized by the exemption of the intake of potentially inflammatory foods, namely gluten, dairy and ultra-processed foods, over a consecutive period of 3 months. During the first month, a low FODMAPs diet will be implemented, along with the anti-inflammatory diet, followed by the reintroduction of all fruits and vegetables over a consecutive period of 2 months, for a total of 3 months of intervention. Group 2 will adopt a diet based on general recommendations for healthy eating in accordance with the World Health Organization. The Ethics Committee of the Portuguese Institute of Rheumathology approved this intervention study. The results of this study are expected to determine whether a change in patient nutrition helps to alleviate symptoms, which would optimize medical intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
Antiinflammatory diet, Low FODMAPs diet, Gluten, casein, sugar and processed-foods free diet, Nutrition

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Anti-inflammatory and low FODMAPs diet
Arm Type
Experimental
Arm Description
The anti-inflammatory diet is characterized by the exclusion of potential inflammatory foods, such as gluten, dairy and processed food, for three months. During the first month, a low FODMAPs diet will be implemented, followed by the reintroduction of all fruits and vegetables over a consecutive period of 2 months. Additionally, some potentially anti-inflammatory foods will be promoted: Omega-3 through specific fish (tuna fish, salmon, sardine, horse mackerel) and nuts, antioxidant rich foods, such as fruit and vegetables, and the maintenance of glycemic index.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Dietary counselling based on general recommendations for healthy eating according to the World Health Organization
Intervention Type
Behavioral
Intervention Name(s)
Anti-inflammatory and low FODMAPs diet
Intervention Description
Exemption of the intake of potentially inflammatory foods, namely gluten, dairy and processed foods, over a consecutive period of 3 months. During the first month, a low FODMAPs diet will be implemented, along with the anti-inflammatory diet, followed by the reintroduction of all fruits and vegetables over a consecutive period of 2 months.
Intervention Type
Behavioral
Intervention Name(s)
General healthy eating
Intervention Description
Healthy eating counseling according to the World Health Organization
Primary Outcome Measure Information:
Title
Change in pain, accessed by Visual Analogue Pain Scale
Description
Accessed by Visual Analogue Pain Scale (1 question about pain intensity over the last month, score: 0-10, with 0 = a total pain relief and 10=the greatest pain ever felt).
Time Frame
1 and 3 months after baseline
Title
Change in pain, accessed by Brief Pain Inventory
Description
Accessed by Brief Pain Inventory (12 questions about pain severity and pain interference; presented with 0-10 scales, with 0=no interference and 10=interferes completely; scale range from 0 to 120 - higher range represent a worst result).
Time Frame
1 and 3 months after baseline
Title
Change in quality of life accessed by Revised Fibromyalgia Impact Questionnaire
Description
Accessed by Revised Fibromyalgia Impact Questionnaire (20 questions about physical functioning (score 0-3, with 0 = optimal and 3 = worst), and about work difficulty, pain, fatigue, morning tiredness, stiffness, anxiety and depression (score 1-10, with 1 = optimal and 10 = worst; scale range from 0 to 117 - higher range represent a worst result).
Time Frame
1 and 3 months after baseline
Title
Change in quality of life accessed by Short-form 36
Description
Accessed by Short-form 36 (36 questions related to the last month, distributed in 8 dimensions: physical function (Score 1-3, with 1 = very limited and 3 = not limited), physical performance, pain, general health, vitality, social function, emotional performance and mental health (score 1-5, with 1 = bad and 5-optimal); scale range from 36 to 142 - higher range represent a worst result).
Time Frame
1 and 3 months after baseline
Title
Change in inflammatory parameters accessed by serum C-reactive protein measurement
Description
Measurement of serum C-reactive protein (mg/L).
Time Frame
3 months after baseline
Title
Change in inflammatory parameters accessed by serum erythrocyte sedimentation rate measurement
Description
Measurement of serum erythrocyte sedimentation rate (mm/h).
Time Frame
3 months after baseline
Title
Change in inflammatory parameters accessed by serum interleukin-8 measurement
Description
Measurement of serum and interleukin-8 (pg/mL).
Time Frame
3 months after baseline
Secondary Outcome Measure Information:
Title
Change in fatigue accessed by Fatigue Severity Survey
Description
Accessed by 1 questionnaire: Fatigue Severity Survey (7 questions with scale from 1 to 7, with 1 = fully disagree and 7 = fully agree; scale range from 7 to 49 - higher range represent a worst result).
Time Frame
1 and 3 months after baseline
Title
Change in gastrointestinal symptoms accessed by Visual Analog Scale from a list of common gastrointestinal symptoms
Description
Accessed by questionnaire: Visual Analog Scale from a list of common gastrointestinal symptoms (10 questions about gastrointestinal discomfort over the last month, score: 0-10, with 0 = none and 10 = a big discomfort; scale range from 0 to 100 - higher range represent a worst result).
Time Frame
1 and 3 months after baseline
Title
Change in quality of sleep accessed by Pittsburgh Sleep Quality Index
Description
Accessed by 1 questionnaire: Pittsburgh Sleep Quality Index (18 questions with a scale from 1 to 4, with 1=no sleep disturbance and 4=to much sleep disturbance; scale range from 18 to 72 - higher range represent a worst result).
Time Frame
1 and 3 months after baseline
Title
Change in weight
Description
Measurement of weight in Kilograms.
Time Frame
3 months after baseline
Title
Change in waist circumference
Description
Measurement of waist circumference in centimeters.
Time Frame
3 months after baseline
Title
Change in body fat mass
Description
Measurement by bio-impedance of body fat mass in percentage.
Time Frame
3 months after baseline

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of FM performed by the physician, according to the Rome III criteria of the American College of Rheumatology, revised in 2010; Ability to read and sign the Informed Consent; Stable dose therapy within 4 weeks before study start. Exclusion Criteria: Patients with pathologies that prevent the follow-up of the given dietary protocol; Patients currently undergoing lactation or pregnancy; Prior or current clinical history of abuse of drug or other substances; Change of therapy during the intervention period; Presence of other inflammatory diseases; Uncontrolled medical conditions (eg. Diabetes Mellitus, decompensated heart disease, renal failure, neoplastic diseases, liver diseases).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ana Rita Silva, MD
Organizational Affiliation
Universidade do Porto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto Português de Reumatologia
City
Lisboa
Country
Portugal

12. IPD Sharing Statement

Citations:
PubMed Identifier
22034969
Citation
Uceyler N, Hauser W, Sommer C. Systematic review with meta-analysis: cytokines in fibromyalgia syndrome. BMC Musculoskelet Disord. 2011 Oct 28;12:245. doi: 10.1186/1471-2474-12-245.
Results Reference
result
PubMed Identifier
30735059
Citation
Silva AR, Bernardo A, Costa J, Cardoso A, Santos P, de Mesquita MF, Vaz Patto J, Moreira P, Silva ML, Padrao P. Dietary interventions in fibromyalgia: a systematic review. Ann Med. 2019;51(sup1):2-14. doi: 10.1080/07853890.2018.1564360.
Results Reference
result
PubMed Identifier
28804483
Citation
Statovci D, Aguilera M, MacSharry J, Melgar S. The Impact of Western Diet and Nutrients on the Microbiota and Immune Response at Mucosal Interfaces. Front Immunol. 2017 Jul 28;8:838. doi: 10.3389/fimmu.2017.00838. eCollection 2017.
Results Reference
result
PubMed Identifier
23941862
Citation
Shivappa N, Steck SE, Hurley TG, Hussey JR, Hebert JR. Designing and developing a literature-derived, population-based dietary inflammatory index. Public Health Nutr. 2014 Aug;17(8):1689-96. doi: 10.1017/S1368980013002115. Epub 2013 Aug 14.
Results Reference
result
PubMed Identifier
36091254
Citation
Silva AR, Bernardo A, de Mesquita MF, Vaz-Patto J, Moreira P, Silva ML, Padrao P. An anti-inflammatory and low fermentable oligo, di, and monosaccharides and polyols diet improved patient reported outcomes in fibromyalgia: A randomized controlled trial. Front Nutr. 2022 Aug 15;9:856216. doi: 10.3389/fnut.2022.856216. eCollection 2022.
Results Reference
derived
PubMed Identifier
33743794
Citation
Silva AR, Bernardo A, de Mesquita MF, Vaz Patto J, Moreira P, Silva ML, Padrao P. A study protocol for a randomized controlled trial of an anti-inflammatory nutritional intervention in patients with fibromyalgia. Trials. 2021 Mar 9;22(1):198. doi: 10.1186/s13063-021-05146-3.
Results Reference
derived

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Anti-inflammatory Nutritional Intervention in Patients With Fibromyalgia

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