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

Depression Clinical Trial

Official title:

Group Therapy for Fibromyalgia: RCT Testing the Effectiveness of Mindfulness -Based Therapy Versus Cognitive-behavioral Therapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04265196
• Other study ID #: 10112019
• Status: Completed
• Phase: N/A
• Start date: April 4, 2019
• Est. completion date: August 31, 2022

Study information

• Verified date: October 2022
• Source: Bar-Ilan University, Israel
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 90
• Est. completion date: August 31, 2022
• Est. primary completion date: October 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

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

Related Conditions & MeSH terms

• Depression
• Dyssomnias
• Fibromyalgia
• Myofascial Pain Syndromes
• Parasomnias
• PTSD
• Sleep Disturbance
• Stress

Intervention

Other:
• cognitive behavioral group therapy
A unique protocol that includes cognitive-behavioral psychological therapy with emphasis on coping with pain
• Mindfulness-based group therapy
Unique protocol that includes mindfulness-based psychological therapy with emphasis on coping with pain

Locations

Country	Name	City	State
Israel	Bar Ilan University	Ramat Gan

Sponsors (2)

Lead Sponsor	Collaborator
Bar-Ilan University, Israel	Maccabi Healthcare Services, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	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	change through study completion, an average of 6 month
Primary	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.	change through study completion, an average of 6 month
Primary	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.	change through study completion, an average of 6 month
Primary	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).	change through study completion, an average of 6 month
Primary	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.	change through study completion, an average of 6 month
Secondary	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	change through study completion, an average of 6 month
Secondary	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.	change through study completion, an average of 6 month
Secondary	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.	change through study completion, an average of 6 month
Secondary	Meta-cognition (MCQ-30)	A self-report questionnaire designed to test metacognitive ability, with an emphasis on beliefs, judgment, and regulation.	change through study completion, an average of 6 month
Secondary	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	change through study completion, an average of 6 month
Secondary	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	change through study completion, an average of 6 month
Secondary	Trauma Exposure (The Life Events Checklist)	An index that examines exposure to traumatic life events. Exposure is rated at various levels (direct, indirect, experience)	Pre-treatment
Secondary	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	change through study completion, an average of 6 month
Secondary	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	change through study completion, an average of 6 month
Secondary	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.	change through study completion, an average of 6 month