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Behavioural Intervention
EMG Biofeedback for Chronic Pain (BEAT-Pain Trial)
N/A
Recruiting
Led By Asimina Lazaridou, PhD
Research Sponsored by Brigham and Women's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 6 months
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a device that helps people relax their muscles. It targets patients with chronic low back pain, those undergoing mastectomy or lumpectomy, and those with episodic migraines. The goal is to see if this device can help reduce their pain and improve their overall well-being.
Who is the study for?
This trial is for English-speaking adults aged 18-65 with chronic low back pain, recent mastectomy or lumpectomy patients, and those with episodic migraines. Participants must have access to a computer or tablet, not be pregnant, and should not have had any changes in certain medications recently. They cannot have serious psychiatric conditions, active addiction disorders, implanted medical devices affecting the spine or nerves, severe sensory impairments, unstable medical conditions that could affect participation or require urgent surgery.
What is being tested?
The study tests EMG biofeedback (EMG-BF) using JOGO Digital Therapeutics devices on pain outcomes for people with chronic low back pain, post-mastectomy/lumpectomy pain and migraines. It involves weekly sessions where participants learn to use the device aimed at muscle relaxation and neuromuscular retraining. The control group receives no active treatment but undergoes baseline testing.
What are the potential side effects?
Since this trial uses non-invasive biofeedback therapy through a device connected to a smartphone or tablet rather than medication or invasive procedures, side effects are minimal but may include skin irritation from electrode placement and potential frustration if difficulties arise while learning to use the technology.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Pain intensity after treatment period
Secondary study objectives
Negative affect (anxiety, depression)
Pain catastrophizing
Pain sensitivity in kPa (pain threshold)
+3 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
6Treatment groups
Experimental Treatment
Active Control
Group I: EMG-Biofeedback for Persistent Post-Mastectomy PainExperimental Treatment1 Intervention
Participants will receive a JOGO Digital Therapeutics EMG Biofeedback device and a software installed on a tablet or smart phone. During the 4 weekly sessions participants will be instructed on how to use the device by a trained biofeedback instructor ahead of their mastectomy.
Group II: EMG-Biofeedback for MigraineExperimental Treatment1 Intervention
Participants will receive a JOGO Digital Therapeutics EMG Biofeedback device and a software installed on a tablet or smart phone. During the 6 weekly sessions participants will be instructed on how to use the device by a trained biofeedback instructor.
Group III: EMG-Biofeedback for Lower Back PainExperimental Treatment1 Intervention
Participants will receive a JOGO Digital Therapeutics EMG Biofeedback device and a software installed on a tablet or smart phone. During the 8 weekly sessions participants will be instructed on how to use the device by a trained biofeedback instructor.
Group IV: Treatment as usual (Lower Back Pain)Active Control1 Intervention
Participants in this group will receive no active treatment.
Group V: Treatment as usual (Migraine)Active Control1 Intervention
Participants in this group will receive no active treatment.
Group VI: Treatment as usual (Persistent Post-Mastectomy Pain)Active Control1 Intervention
Participants in this group will receive no active treatment.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Chronic Lower Back Pain (CLBP) include EMG-Biofeedback, cognitive-behavioral therapy (CBT), mindfulness-based stress reduction (MBSR), and various exercise therapies. EMG-Biofeedback works by facilitating neuromuscular retraining and muscle relaxation through audio and visual stimuli, helping patients gain control over muscle tension and reduce pain.
CBT helps patients manage pain by changing negative thought patterns and behaviors, leading to reduced distress and improved coping strategies. MBSR focuses on mindfulness and meditation techniques to reduce stress and enhance pain management.
Exercise therapies, including core stabilization and directional preference exercises, improve physical function and reduce pain by strengthening muscles and promoting proper movement patterns. These treatments are important for CLBP patients as they offer non-pharmacological options that address both the physical and psychological components of chronic pain, leading to better overall pain management and quality of life.
The use of EMG feedback and progressive relaxation in the treatment of a woman with chronic back pain.Effectiveness of CAM therapy: understanding the evidence.Effects of electromyography biofeedback-assisted relaxation on pain in patients with advanced cancer in a palliative care unit.
The use of EMG feedback and progressive relaxation in the treatment of a woman with chronic back pain.Effectiveness of CAM therapy: understanding the evidence.Effects of electromyography biofeedback-assisted relaxation on pain in patients with advanced cancer in a palliative care unit.
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Who is running the clinical trial?
Brigham and Women's HospitalLead Sponsor
1,664 Previous Clinical Trials
11,834,656 Total Patients Enrolled
Asimina Lazaridou, PhD5.01 ReviewsPrincipal Investigator - Brigham and Women's Hospital
Brigham and Women's Hospital
1 Previous Clinical Trials
135 Total Patients Enrolled
5Patient Review
Dr. Mina was very kind and easy to talk to. She was also clearly very experienced in the field of pain psychology, and was able to provide me with helpful strategies and tools that I could use to manage my chronic pain. Overall, she helped me to feel more confident and hopeful, and I am very grateful to her for that.
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have a severe mental health condition like schizophrenia, delusional disorder, or psychotic disorder that has required hospitalization in the past year and could affect your ability to take part in the study.You have had an allergic skin reaction to tapes and plasters in the past.You are between 18 and 65 years old.You have another ongoing pain condition that you find more painful than chronic lower back pain.Your lower back pain is caused by something other than a physical injury, like a tumor, infection, or inflammation.You are currently receiving treatment for cancer such as chemotherapy or radiation.You have a serious problem with your vision or hearing.You have a medical device implanted in your body, such as a spinal cord stimulator or nerve stimulator.You have been diagnosed with mild memory problems or dementia.You have thoughts about hurting yourself and the doctor knows about it.You have moderate or severe depression, or you scored 3 or higher on the PHQ-2 questionnaire.You have been hospitalized for a mental health condition in the past year, as reported by yourself.You have a painful condition that you feel is worse than migraine.You start a new treatment for migraines during the study.You have a medical condition that affects your ability to feel pain or take part in the EMG treatment. For example, HIV, peripheral neuropathy, or Raynaud's syndrome.You have had ongoing low back pain for at least 6 months but not longer than 10 years.Your pain level is higher than 3 on a pain scale at the beginning of the sessions.You have had significant pain in your body recently, rated as more than 1 on a pain scale.Women between 18 and 65 years old.You have been diagnosed with episodic migraine, with or without aura, according to specific medical guidelines.You have had migraines for 4 to 14 days in the last month.You have experienced migraines for more than a year, based on your own reports.You had surgery on your lower back in the last year.You have a painful condition that needs immediate surgery.You are currently addicted to drugs like cocaine or heroin that could make it hard for you to take part in the study.
Research Study Groups:
This trial has the following groups:- Group 1: EMG-Biofeedback for Lower Back Pain
- Group 2: Treatment as usual (Lower Back Pain)
- Group 3: EMG-Biofeedback for Persistent Post-Mastectomy Pain
- Group 4: EMG-Biofeedback for Migraine
- Group 5: Treatment as usual (Migraine)
- Group 6: Treatment as usual (Persistent Post-Mastectomy Pain)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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