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Chronic Pain and Conditioned Pain Modulation After on Line-behavioral Approach (Be-Home-Pain)

Primary Purpose

Migraine

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Mindfullness
treatment as usual (TAU) (pharmacological)
Sponsored by
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Migraine focused on measuring Chronic Pain;, Chronic Migraine;, Conditioned Pain Modulation;, Mindfulness;

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of chronic Migraine and Chronic Neuropathic Pain
  • Written informed consent

Exclusion Criteria:

  • Co-existent severe medical or psychiatric illnesses
  • Use of opioids during the 3 months before the inclusion into the protocol
  • Practice of mindfulness in the last 12 months

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Other

    Arm Label

    Treatment as usual (TAU)

    TAU plus behavioral approach

    Arm Description

    Any pharmacological therapy used for managing chronic pain or chronic migraine

    Any pharmacological therapy used for managing chronic pain or chronic migraine added with behavioral approach (mindfulness) delivered on line and smart phone for 6 weekly sessions

    Outcomes

    Primary Outcome Measures

    Change of pain intensity
    Mean NRS (Numerical Rating Scale evaluation from the Daily diary card ) difference of at least 2 points on the scale(the scale range is from 0=no pain to 10 =maximum pain perceived) between MIND/TAU and TAU groups assessed by the daily diary card.

    Secondary Outcome Measures

    Change of pain frequency
    Decrease in pain frequency, (days of pain per month) assessed by Daily Diary Card.
    Change of medication intake
    Decrease of number of symptomatic medications per month assessed by Daily Diary Card.
    Neurophysiological indexes
    Changes in neurophysiological indexes evaluated by quantitative sensory test for conditioned pain modulation analysis.
    Psychological measures - coping strategies
    Pain Catastrophizing Scale-Italian, PCS-I (Monticone et al., 2012) cut-off: 0 - 30 normal ranges > 30 abnormal
    Psychological measures - Quality of life
    General Self-Efficacy Scale, GSE ( (Schwarzer et al., 1995) cut off: 0 - 10 abnormal 10 - 40 normal ranges
    Psychological measures - Mood
    Hospital Anxiety and Depression Scale, HADS (Costantini et al., 1999) cut-off: total score 0 -7 = normal total score > 7 = impairment
    Psychological measures - Mindfulness specific tests
    Mindful Awareness Attention Scale, MAAS (Veneziani et al., 2015) for mindfulness attitude for patients randomized in the MIND/TAU group cut-off: 15 - 90 normal ranges

    Full Information

    First Posted
    March 31, 2021
    Last Updated
    July 28, 2021
    Sponsor
    Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04859374
    Brief Title
    Chronic Pain and Conditioned Pain Modulation After on Line-behavioral Approach
    Acronym
    Be-Home-Pain
    Official Title
    Effectiveness of Home- Behavioral Approach by Mindfulness Added to Pharmacological Treatment on Endogenous Pain Modulation in Patients With Chronic Pain: Results at Long-term (Be-Home-Pain)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 2021 (Anticipated)
    Primary Completion Date
    May 2022 (Anticipated)
    Study Completion Date
    May 2022 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta

    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
    Chronic pain is a disabling condition associated with progressive changes and decline in psychological wellbeing. According with a modern conceptualization, pain has to be considered a biopsychosocial disorder where biological, affective, social and psychological aspects are strictly connected. Although this new conceptualization, the implementation of an integral systems approach of psychological tenets into treatments for chronic pain are limited. Concerning treatments of chronic pain condition, the literature of the last years has demonstrated how clinical benefit can be improved when traditional therapies are combined with behavioral approaches in particular mindfulness. Systemic quantitative-somatosensory testing of Conditioned Pain Modulation (CPM) can be considered a measure of endogenous modulation of pain and it has been used in different clinical experiences to evaluate the effectiveness of different pain treatments even if non pharmacological approaches.
    Detailed Description
    Chronic pain is a disabling condition associated with progressive changes and decline in psychological wellbeing. The burden of this condition is significant and also the epidemiological impact. According with a modern conceptualization, pain has to be considered a biopsychosocial disorder where biological, affective, social and psychological aspects are strictly connected. Although this new conceptualization, the implementation of an integral systems approach of psychological tenets into treatments for chronic pain are limited. Concerning treatment of chronic pain condition, the literature of the last years has demonstrated how clinical benefit can be improved when traditional therapies are combined with behavioral approaches in particular mindfulness, that help patients to become more conscious about their symptoms and able to manage pain without medication. Systemic quantitative-somatosensory testing of Conditioned Pain Modulation (CPM) can be considered a measure of endogenous modulation of pain and it has been used in different clinical experiences to evaluate the effectiveness of different pain treatments even if non pharmacological approaches Aim of this study: A group of patients suffering from Chronic Migraine and Chronic Neuropathic Pain will be studied and followed with a specific mindfulness protocol, added to traditional pharmacological therapy, performed on-line for 8 weeks. In order to determine if the behavioral approach can improve their clinical condition patients will be followed for 12 months after treatments with regular visits every 3 months. Also, in order to assess the integrity and improvement of the endogenous pain inhibitory control a conditioned pain modulation paradigm will be performed at baseline and at 3, 6, 12 months. Patients will perform a baseline evaluation of thermal pain and mechanical pain tresholds using the quantitative sensory methods, including the determination of heat-generated temporal summation. Then, at baseline and at 3, 6, 12 months follow up, the CPM paradigm will be performed using two heat painful stimuli, a tonic heat stimulus as conditioning stimulus and a phasic heat stimulus as test stimuli. Patients will be treated by traditional pharmacological therapies added to behavioral approach (mindfulness on line by using a specific platform (STARLEAF)) (TAU/MIND) Eight weekly one-hour video-sessions of mindfulness practice will be scheduled for patients; instructions to manage pain and to encourage the use of strategies for pain management will be given. Moreover, instructions for behavioral approach and mindfulness, to practice every day will be given: daily standardized mindfulness sessions of 12 minutes, by smartphone, recorded by the expert who generally manages their sessions at the hospital will be scheduled for patients Neuropsychological assessment will be provided at baseline and at every follow up Clinical, neurophysiological and neuropsychological results will be compared to those obtained from another group of patients treated by traditional pharmacological treatment (TAU) This preliminary study will be conducted on 35 patients with diagnosis of CM and Chronic Neuropathic Pain performed at our center. Specific questionnaires for cognitive assessment and disability, catastrophizing attitude, anxiety, depression, acceptance, pain coping will be performed at baseline and repeated at every follow up ( PCS; GSE; HADS; CPAQ; AAQ; MAAS). The pain diary will be checked too with scheduled NSR evaluation. The questionnaires will be repeated at every follow up and the pain diary will be evaluated. Results will be collected at baseline up to 12 months after treatment for both groups.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Migraine
    Keywords
    Chronic Pain;, Chronic Migraine;, Conditioned Pain Modulation;, Mindfulness;

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Masking Description
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    35 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Treatment as usual (TAU)
    Arm Type
    Other
    Arm Description
    Any pharmacological therapy used for managing chronic pain or chronic migraine
    Arm Title
    TAU plus behavioral approach
    Arm Type
    Other
    Arm Description
    Any pharmacological therapy used for managing chronic pain or chronic migraine added with behavioral approach (mindfulness) delivered on line and smart phone for 6 weekly sessions
    Intervention Type
    Behavioral
    Intervention Name(s)
    Mindfullness
    Intervention Description
    Behavioral approach (mindfulness) delivered on line and smart phone for 6 weekly sessions
    Intervention Type
    Drug
    Intervention Name(s)
    treatment as usual (TAU) (pharmacological)
    Intervention Description
    Any pharmacological therapy used for managing chronic pain or chronic migraine
    Primary Outcome Measure Information:
    Title
    Change of pain intensity
    Description
    Mean NRS (Numerical Rating Scale evaluation from the Daily diary card ) difference of at least 2 points on the scale(the scale range is from 0=no pain to 10 =maximum pain perceived) between MIND/TAU and TAU groups assessed by the daily diary card.
    Time Frame
    From the first visit to the first follow up at 3 months till the last follow up at 12 months
    Secondary Outcome Measure Information:
    Title
    Change of pain frequency
    Description
    Decrease in pain frequency, (days of pain per month) assessed by Daily Diary Card.
    Time Frame
    6 and 12 months
    Title
    Change of medication intake
    Description
    Decrease of number of symptomatic medications per month assessed by Daily Diary Card.
    Time Frame
    6 and 12 months
    Title
    Neurophysiological indexes
    Description
    Changes in neurophysiological indexes evaluated by quantitative sensory test for conditioned pain modulation analysis.
    Time Frame
    3, 6 and 12 months
    Title
    Psychological measures - coping strategies
    Description
    Pain Catastrophizing Scale-Italian, PCS-I (Monticone et al., 2012) cut-off: 0 - 30 normal ranges > 30 abnormal
    Time Frame
    6 and 12 months
    Title
    Psychological measures - Quality of life
    Description
    General Self-Efficacy Scale, GSE ( (Schwarzer et al., 1995) cut off: 0 - 10 abnormal 10 - 40 normal ranges
    Time Frame
    6 and 12 months
    Title
    Psychological measures - Mood
    Description
    Hospital Anxiety and Depression Scale, HADS (Costantini et al., 1999) cut-off: total score 0 -7 = normal total score > 7 = impairment
    Time Frame
    6 and 12 months
    Title
    Psychological measures - Mindfulness specific tests
    Description
    Mindful Awareness Attention Scale, MAAS (Veneziani et al., 2015) for mindfulness attitude for patients randomized in the MIND/TAU group cut-off: 15 - 90 normal ranges
    Time Frame
    6 and 12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of chronic Migraine and Chronic Neuropathic Pain Written informed consent Exclusion Criteria: Co-existent severe medical or psychiatric illnesses Use of opioids during the 3 months before the inclusion into the protocol Practice of mindfulness in the last 12 months
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Licia Grazzi, MD
    Phone
    +39022394
    Ext
    2366
    Email
    licia.grazzi@istituto-besta.it
    First Name & Middle Initial & Last Name or Official Title & Degree
    Renato Mantegazza, MD
    Phone
    +39022394
    Ext
    2321
    Email
    crc@istituto-besta.it

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Chronic Pain and Conditioned Pain Modulation After on Line-behavioral Approach

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