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Mindfulness + tVNS for Chronic Kidney Disease (MIND-CKD Trial)
N/A
Recruiting
Led By Jeanie Park
Research Sponsored by Emory University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Stages III and IV CKD as defined by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) creatinine equation
Be older than 18 years old
Must not have
Carotid atherosclerosis
Uncontrolled hypertension (BP≥170/100 mm Hg)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 8 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial tests if mindfulness meditation and a device that sends electrical pulses to a nerve can help people with chronic kidney disease. These treatments aim to reduce stress and balance the nervous system, potentially improving heart health.
Who is the study for?
This trial is for adults with stable chronic kidney disease stages III and IV, without recent heart attacks or strokes, severe CKD, certain nerve conditions, extreme blood pressure levels, heavy substance use, or major surgeries in the past 3 months. Pregnant individuals or those on specific medications like MAO inhibitors are excluded.
What is being tested?
The study examines if mindfulness meditation can improve nervous system function in CKD patients and whether adding non-invasive vagus nerve stimulation enhances these benefits compared to a sham (fake) treatment.
What are the potential side effects?
Potential side effects may include discomfort at the stimulation site for tVNS users. Mindfulness programs are generally low-risk but could cause emotional distress or fatigue.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My kidney function is moderately to severely reduced.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have hardening of the arteries in my neck.
Select...
My blood pressure is not higher than 170/100 mm Hg.
Select...
I am currently taking central α-agonists or MAO inhibitors.
Select...
My kidney function is severely reduced.
Select...
I have nerve damage due to diabetes.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 8 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in mean Muscle Sympathetic Nerve Activity (MSNA) burst frequency (BF)
Secondary study objectives
Body Weight Changes
Change in baroreflex sensitivity (BRS)
Change in daytime burst frequency (BF)
+1 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: Mindfulness-Based Stress Reduction (MBSR)Experimental Treatment1 Intervention
Mindfulness-Based Stress Reduction (MBSR) tis designed to provide education about mindfulness and stress; experiential mindfulness practice, and discussion of participants' experiences with mindfulness practice. MBSR is delivered in 8 weekly 2.5-hour group sessions and one day-long retreat that occurs after the 6th session.
Group II: MBSR+tVNSExperimental Treatment2 Interventions
Mindfulness-Based Stress Reduction (MBSR) tis designed to provide education about mindfulness and stress; experiential mindfulness practice, and discussion of participants' experiences with mindfulness practice. MBSR is delivered in 8 weekly 2.5-hour group sessions and one day-long retreat that occurs after the 6th session.
Transcutaneous vagus nerve stimulation (tVNS) is a simple, noninvasive, self-administered adjunctive therapy, that may enhance the sympatho-inhibitory effects of mindfulness meditation (MM) in chronic kidney disease (CKD) .
Group III: HEP+tVNSExperimental Treatment2 Interventions
Health enhancement program (HEP) is designed to provide a structurally parallel, active control intervention to MBSR with health benefits in their own right, while omitting any components of mindfulness. HEP participants will meet with a health educator (a registered dietician) in a group setting for 8 weekly 2.5-hour sessions.
Transcutaneous vagus nerve stimulation (tVNS) is a simple, noninvasive, self-administered adjunctive therapy, that may enhance the sympatho-inhibitory effects of mindfulness meditation (MM) in chronic kidney disease (CKD).
Group IV: MBSR+sham-tVNSActive Control2 Interventions
Mindfulness-Based Stress Reduction (MBSR) tis designed to provide education about mindfulness and stress; experiential mindfulness practice, and discussion of participants' experiences with mindfulness practice. MBSR is delivered in 8 weekly 2.5-hour group sessions and one day-long retreat that occurs after the 6th session.
Sham stimulation will be delivered using a sham device that is identical in appearance and function to tVNS, but programmed to produce a lower frequency biphasic signal that can be felt by the participant without actually stimulating the vagus nerve.
Group V: Health enhancement program (HEP)Active Control1 Intervention
Health enhancement program (HEP) is designed to provide a structurally parallel, active control intervention to MBSR with health benefits in their own right, while omitting any components of mindfulness. HEP participants will meet with a health educator in a group setting for 8 weekly 2.5-hour sessions with a day-long retreat.
Group VI: HEP+sham-tVNSActive Control2 Interventions
Health enhancement program (HEP) is designed to provide a structurally parallel, active control intervention to MBSR with health benefits in their own right, while omitting any components of mindfulness. HEP participants will meet with a health educator in a group setting for 8 weekly 2.5-hour sessions.
Sham stimulation is be delivered using a sham device that is identical in appearance and function to tVNS, but programmed to produce a lower frequency (0.1 Hz) biphasic signal that can be felt by the participant without actually stimulating the vagus nerve.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Mindfulness-based stress reduction (MBSR)
2014
N/A
~250
Transcutaneous Vagus Nerve Stimulation (tVNS)
2018
Completed Phase 2
~40
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
Mindfulness Meditation (MM) and Transcutaneous Vagus Nerve Stimulation (tVNS) are emerging treatments for Chronic Kidney Disease (CKD) that focus on modulating the autonomic nervous system. MM improves sympathetic function by reducing stress and promoting relaxation, which can lower blood pressure and improve kidney function. tVNS stimulates the vagus nerve to enhance its inhibitory effects on the sympathetic nervous system, restoring autonomic balance.
This can reduce inflammation, lower blood pressure, and improve heart rate variability, all of which are beneficial for slowing the progression of CKD.
Hemodynamic theory of progressive renal disease: a 10-year update in brief review.Current therapeutic strategies in cardiorenal syndrome.Rapidly deteriorating renal function with membranoproliferative glomerulonephritis Type 1 associated with hepatitis C treated successfully with steroids and antiviral therapy: a case report and review of literature.
Hemodynamic theory of progressive renal disease: a 10-year update in brief review.Current therapeutic strategies in cardiorenal syndrome.Rapidly deteriorating renal function with membranoproliferative glomerulonephritis Type 1 associated with hepatitis C treated successfully with steroids and antiviral therapy: a case report and review of literature.
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Who is running the clinical trial?
Emory UniversityLead Sponsor
1,697 Previous Clinical Trials
2,603,768 Total Patients Enrolled
National Center for Complementary and Integrative Health (NCCIH)NIH
854 Previous Clinical Trials
671,610 Total Patients Enrolled
Jeanie ParkPrincipal Investigator - Emory University
Emory University Hospital, Emory University Hospital Midtown, Select Specialty Hospital-Atlanta
University Of Alabama School Of Medicine (Medical School)
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You regularly drink more than two drinks a day if you're a man, or more than one drink a day if you're a woman.Your hemoglobin level is less than 10 grams per deciliter, which means you have severe anemia.Your heart beats too slowly, less than 55 times per minute.Your blood pressure is lower than 100/50 mm Hg.You are using another device that stimulates your nerves, like a TENS unit.You have a pacemaker or other implanted electronic or metal device.I have had surgery in the last 3 months.I have not had a heart attack or stroke in the last 6 months.You have a severe mental disorder that can cause you to lose touch with reality.I do not have any serious illnesses that could affect my survival.Problems with your body's automatic functions.You have thoughts of wanting to harm yourself.I have not changed my blood pressure medicine in the last month.I have hardening of the arteries in my neck.My blood pressure is not higher than 170/100 mm Hg.My kidney function is moderately to severely reduced.You have a hearing aid or any metal implant near your neck.My kidney function has been stable for the last 3 months.I am currently taking central α-agonists or MAO inhibitors.My kidney function is severely reduced.I have nerve damage due to diabetes.
Research Study Groups:
This trial has the following groups:- Group 1: MBSR+sham-tVNS
- Group 2: MBSR+tVNS
- Group 3: HEP+tVNS
- Group 4: Health enhancement program (HEP)
- Group 5: Mindfulness-Based Stress Reduction (MBSR)
- Group 6: HEP+sham-tVNS
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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