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Group Therapy for Fibromyalgia:the Effectiveness of Mindfulness -Based VS Cognitive-behavioral Therapy

Primary Purpose

Fibromyalgia, PTSD, Depression

Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
cognitive behavioral group therapy
Mindfulness-based group therapy
Sponsored by
Bar-Ilan University, Israel
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed with fibromyalgia
  • Hebrew speakers

Exclusion Criteria:

  • Patients who are actively suicidal
  • Patients who suffering from psychotic status
  • Patients who are chronically use addictive substances,
  • Patients who had unusual cognitive or physical disability that would prevent them from participating in mindfulness exercises

Sites / Locations

  • Bar Ilan University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

cognitive behavioral group therapy

Mindfulness-based group therapy

control group

Arm Description

A Cognitive Behavioral Therapy intervention is based on a unique protocol built in the light of previous research in the field and includes a 10-week treatment focused on coping with pain and stress.

A mindfulness-based group therapy intervention was built inspired by a mindfulness protocol that is effective in treating pain, and includes adjustments to the physical distress of fibromyalgia patients as well as an emphasis on coping with stress and pain.

A control group will wait for 3 months, during which the subjects will complete the questionnaires and only after the end of the period will they participate in the treatment so that it will serve as a control group without intervention.

Outcomes

Primary Outcome Measures

The Fibromyalgia Impact Questionnaire Revised (FIQR)
Self-report questionnaire, which includes 21 items and assesses symptoms and functioning of fibromyalgia patients, taking into account the frequency of symptoms, their intensity, and the degree of impairment of patient function
Perceived Stress Scale (PSS)
A 10-item questionnaire measuring the level at which events occurred in the individual's life in the past month is perceived as unpredictable, uncontrollable and overwhelming. A higher score indicates a higher level of perceived stress.
The Patient Health Questionnaire-9 (PHQ-9)
A self-reported 9-item questionnaire to measure symptoms of major depression. The items relate to the key aspects of DSM, including thoughts of death, loss of appetite, sadness and mental pain, and negative cognitions.
Pain (VAS)
Self-report questionnaire designed to measure pain intensity and unpleasantness caused by pain. This questionnaire is widely used in pain clinics. It includes one item that can be graded on a continuous scale that ranges from 0 (no pain) to 10 (the worst pain that can be).
Sleep Quality (Pittsburgh Sleep Quality Index)
A questionnaire developed to measure sleep quality and sleep disorder. The questionnaire includes 19 items measuring seven components of sleep (sleep quality, sleep onset, sleep duration, sleep efficiency, sleep disturbance, sleep medication use, and daily functioning impairment) over the past four weeks.

Secondary Outcome Measures

Mindfulness (Five Fact Mindfulness Questionnaire)
The questionnaire includes 5 scales, which relate to various mindfulness factors - observing / paying attention to internal and external stimuli , the ability to verbally describe or label stimuli, behavior, non-judgmental and non-reactivity
Psychological Inflexibility in Pain (PIPS)
A questionnaire designed to assess the extent to which a person is trying to control and struggle with physical pain, as opposed to trying and accepting it, and "making friends" with him. The questionnaire includes 12 items.
Body Vigilance (BVS)
Self-report questionnaire designed to examine attention regarding normal physical processes, periodic susceptibility / rhythm sensitivity, and ability to predict physical responses. Each item in the questionnaire is rated on a 7-rank Likert scale (1 = not at all true, 7 = very true), with a higher score representing a higher body awareness.
Meta-cognition (MCQ-30)
A self-report questionnaire designed to test metacognitive ability, with an emphasis on beliefs, judgment, and regulation.
Difficulties in emotion regulation (DERS)
Self-report questionnaire designed to test difficulties in the emotional regulation process. The questionnaire contains 36 items that relate to awareness of emotions and emotional reactions
Pain Catastrophizing (PCS)
A questionnaire examining the tendency to intensify the threat and sense of helplessness arising from pain, and the inability to prevent it
Trauma Exposure (The Life Events Checklist)
An index that examines exposure to traumatic life events. Exposure is rated at various levels (direct, indirect, experience)
Self- Compassion (SCS)
Self-report questionnaire that examines the participant's compassionate ability. The questionnaire refers to 3 components of compassion - Self-Kindness, Common Humanity and Mindfulness
Distress tolerance
Self-report questionnaire covering four different categories: perceived ability to bear emotional distress, subjective assessment of distress, attentiveness to negative emotions, and regulation efforts to reduce distress. A combination of categories allows for an overall measure of distress resistance
Alexithymia
Self-Reporting Questionnaire Examining three subscales: (1) difficulty identifying feelings and distinguishing between feelings and bodily sensations in emotional activation, (2) difficulty in the verbal expression of emotions, and (3) externally oriented thinking.

Full Information

First Posted
February 2, 2020
Last Updated
October 1, 2022
Sponsor
Bar-Ilan University, Israel
Collaborators
Maccabi Healthcare Services, Israel
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1. Study Identification

Unique Protocol Identification Number
NCT04265196
Brief Title
Group Therapy for Fibromyalgia:the Effectiveness of Mindfulness -Based VS Cognitive-behavioral Therapy
Official Title
Group Therapy for Fibromyalgia: RCT Testing the Effectiveness of Mindfulness -Based Therapy Versus Cognitive-behavioral Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
April 4, 2019 (Actual)
Primary Completion Date
October 1, 2021 (Actual)
Study Completion Date
August 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bar-Ilan University, Israel
Collaborators
Maccabi Healthcare Services, Israel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study was conducted as part of a collaboration between the Maccabi Health Fund and Bar Ilan University. Fibromyalgia is a chronic pain disorder, highly co-morbid with depression, stress, and anxiety. the investigators aim to examine the effect of group cognitive-behavioral therapy (CBT) and mindfulness-based intervention (MBI) among fibromyalgia patients. the investigators will also examine which intervention fits which patient, according to one's individual characteristics, in hope that this would enable Maccabi to offer personalized treatment. Furthermore, the investigators wish to identify the underlying cognitive and psychopathological mechanisms (measured during treatment) by which each intervention works.
Detailed Description
Fibromyalgia is a chronic pain disorder, highly co-morbid with depression, stress, and anxiety. the investigators aim to examine the effect of group cognitive-behavioral therapy (CBT) and mindfulness-based intervention (MBI) among fibromyalgia patients. the investigators will also examine which intervention fits which patient, according to one's individual characteristics, in hope that this would enable Maccabi to offer personalized treatment. Furthermore, the investigators wish to identify the underlying cognitive and psychopathological mechanisms (measured during treatment) by which each intervention works. First, the investigators expect that CBT and MBI will lead to greater improvement in physical, psychological, and behavioral measures among fibromyalgia patients compared to waitlist controls. Second, the investigators expect that MBI and CBT will have a differential effect, so that some outcome variables will show greater improvement following one intervention, but not the other. Furthermore, factors such as age, illness duration, symptom severity, and initial psychopathology levels will affect one's level of improvement following these interventions. Finally, the investigators expect to identify differential mechanisms driving each intervention. The study is a randomized controlled trial (RCT), including 90 fibromyalgia patients, randomly assigned to 3 conditions: (1) Group CBT (n=30), (2) MBI (n=30), (3) Waitlist control group, subsequently assigned to treatment (n=30). Participants will complete selfreport questionnaires tapping psychological (depression, stress), cognitive (observing negative experiences "from afar", cognitive flexibility towards pain) and physical (pain, body awareness) aspects, at 4 assessments: pre-/during/post- treatment, and 3 months after treatment. To date, no RCT comparing CBT and MBI for fibromyalgia was conducted. Comparing them would be highly important, as they are the two most notable psychological interventions for chronic pain conditions. This study would enable Maccabi to offer improved psychological services for fibromyalgia. Furthermore, group therapy may serve as an effective treatment meeting both Maccabi's needs (a short, economic intervention) and patients' needs (a condition-specific treatment, offering group support and stigma reduction).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia, PTSD, Depression, Stress, Sleep Disturbance

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Participant
Masking Description
Subjects will be assigned to the different treatment groups randomly and without receiving information about the different treatment options included in the study.
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
cognitive behavioral group therapy
Arm Type
Experimental
Arm Description
A Cognitive Behavioral Therapy intervention is based on a unique protocol built in the light of previous research in the field and includes a 10-week treatment focused on coping with pain and stress.
Arm Title
Mindfulness-based group therapy
Arm Type
Experimental
Arm Description
A mindfulness-based group therapy intervention was built inspired by a mindfulness protocol that is effective in treating pain, and includes adjustments to the physical distress of fibromyalgia patients as well as an emphasis on coping with stress and pain.
Arm Title
control group
Arm Type
No Intervention
Arm Description
A control group will wait for 3 months, during which the subjects will complete the questionnaires and only after the end of the period will they participate in the treatment so that it will serve as a control group without intervention.
Intervention Type
Other
Intervention Name(s)
cognitive behavioral group therapy
Intervention Description
A unique protocol that includes cognitive-behavioral psychological therapy with emphasis on coping with pain
Intervention Type
Other
Intervention Name(s)
Mindfulness-based group therapy
Intervention Description
Unique protocol that includes mindfulness-based psychological therapy with emphasis on coping with pain
Primary Outcome Measure Information:
Title
The Fibromyalgia Impact Questionnaire Revised (FIQR)
Description
Self-report questionnaire, which includes 21 items and assesses symptoms and functioning of fibromyalgia patients, taking into account the frequency of symptoms, their intensity, and the degree of impairment of patient function
Time Frame
change through study completion, an average of 6 month
Title
Perceived Stress Scale (PSS)
Description
A 10-item questionnaire measuring the level at which events occurred in the individual's life in the past month is perceived as unpredictable, uncontrollable and overwhelming. A higher score indicates a higher level of perceived stress.
Time Frame
change through study completion, an average of 6 month
Title
The Patient Health Questionnaire-9 (PHQ-9)
Description
A self-reported 9-item questionnaire to measure symptoms of major depression. The items relate to the key aspects of DSM, including thoughts of death, loss of appetite, sadness and mental pain, and negative cognitions.
Time Frame
change through study completion, an average of 6 month
Title
Pain (VAS)
Description
Self-report questionnaire designed to measure pain intensity and unpleasantness caused by pain. This questionnaire is widely used in pain clinics. It includes one item that can be graded on a continuous scale that ranges from 0 (no pain) to 10 (the worst pain that can be).
Time Frame
change through study completion, an average of 6 month
Title
Sleep Quality (Pittsburgh Sleep Quality Index)
Description
A questionnaire developed to measure sleep quality and sleep disorder. The questionnaire includes 19 items measuring seven components of sleep (sleep quality, sleep onset, sleep duration, sleep efficiency, sleep disturbance, sleep medication use, and daily functioning impairment) over the past four weeks.
Time Frame
change through study completion, an average of 6 month
Secondary Outcome Measure Information:
Title
Mindfulness (Five Fact Mindfulness Questionnaire)
Description
The questionnaire includes 5 scales, which relate to various mindfulness factors - observing / paying attention to internal and external stimuli , the ability to verbally describe or label stimuli, behavior, non-judgmental and non-reactivity
Time Frame
change through study completion, an average of 6 month
Title
Psychological Inflexibility in Pain (PIPS)
Description
A questionnaire designed to assess the extent to which a person is trying to control and struggle with physical pain, as opposed to trying and accepting it, and "making friends" with him. The questionnaire includes 12 items.
Time Frame
change through study completion, an average of 6 month
Title
Body Vigilance (BVS)
Description
Self-report questionnaire designed to examine attention regarding normal physical processes, periodic susceptibility / rhythm sensitivity, and ability to predict physical responses. Each item in the questionnaire is rated on a 7-rank Likert scale (1 = not at all true, 7 = very true), with a higher score representing a higher body awareness.
Time Frame
change through study completion, an average of 6 month
Title
Meta-cognition (MCQ-30)
Description
A self-report questionnaire designed to test metacognitive ability, with an emphasis on beliefs, judgment, and regulation.
Time Frame
change through study completion, an average of 6 month
Title
Difficulties in emotion regulation (DERS)
Description
Self-report questionnaire designed to test difficulties in the emotional regulation process. The questionnaire contains 36 items that relate to awareness of emotions and emotional reactions
Time Frame
change through study completion, an average of 6 month
Title
Pain Catastrophizing (PCS)
Description
A questionnaire examining the tendency to intensify the threat and sense of helplessness arising from pain, and the inability to prevent it
Time Frame
change through study completion, an average of 6 month
Title
Trauma Exposure (The Life Events Checklist)
Description
An index that examines exposure to traumatic life events. Exposure is rated at various levels (direct, indirect, experience)
Time Frame
Pre-treatment
Title
Self- Compassion (SCS)
Description
Self-report questionnaire that examines the participant's compassionate ability. The questionnaire refers to 3 components of compassion - Self-Kindness, Common Humanity and Mindfulness
Time Frame
change through study completion, an average of 6 month
Title
Distress tolerance
Description
Self-report questionnaire covering four different categories: perceived ability to bear emotional distress, subjective assessment of distress, attentiveness to negative emotions, and regulation efforts to reduce distress. A combination of categories allows for an overall measure of distress resistance
Time Frame
change through study completion, an average of 6 month
Title
Alexithymia
Description
Self-Reporting Questionnaire Examining three subscales: (1) difficulty identifying feelings and distinguishing between feelings and bodily sensations in emotional activation, (2) difficulty in the verbal expression of emotions, and (3) externally oriented thinking.
Time Frame
change through study completion, an average of 6 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with fibromyalgia Hebrew speakers Exclusion Criteria: Patients who are actively suicidal Patients who suffering from psychotic status Patients who are chronically use addictive substances, Patients who had unusual cognitive or physical disability that would prevent them from participating in mindfulness exercises
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danny Horesh, Phd
Organizational Affiliation
Bar Ilan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bar Ilan University
City
Ramat Gan
Country
Israel

12. IPD Sharing Statement

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Group Therapy for Fibromyalgia:the Effectiveness of Mindfulness -Based VS Cognitive-behavioral Therapy

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