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Auricular Vagus Stimulation in Obesity

Primary Purpose

Vagus Nerve Stimulation, Obesity

Status
Recruiting
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
Active TENS
Sham TENS
Sponsored by
National Medical Research Center for Therapy and Preventive Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vagus Nerve Stimulation focused on measuring auricular stimulation, auricular vagus nerve stimulation, blinding (masking), transcutaneous vagus nerve stimulation (TENS), vagus nerve stimulation (VNS), obesity abdominal, nutrition disorders, overweight, body weight, active TENS, sham TENS, heart rate, total fat, body mass index, waist circumference, hip circumference, Heart rate variability, quality of life

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Adult patients with grade 1-2 nutritional obesity who are willing and able to give informed written consent to participate in the study, are on sinus rhythm and are not taking any antiarrhythmic drugs, including beta-blockers.

Exclusion Criteria:

  • Cardiac arrhythmias: bradyarrhythmias, Atrioventricular blockades of any degree;
  • Taking beta blockers;
  • The endocrine nature of obesity;
  • Expected technical difficulties when using the device on the part of the patient;
  • Pregnant or plan on becoming pregnant or breastfeeding during the study period;
  • Presence of an electrically, magnetically or mechanically activated implant, an intracerebral vascular clip, or any other electrically sensitive support system.

Sites / Locations

  • National Medical Research Center for Therapy and Preventive MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Active TENS

Sham TENS

Arm Description

Active will be performed with using a TENS device with an ear clip attached to the tragus of the right ear (which is innervated by auricular branch of the vagus nerve) at 25 Hz, 200ms at a current just below discomfort threshold.

Sham TENS will be performed to the ear lobe, which is devoid of vagal innervation.

Outcomes

Primary Outcome Measures

Percentage of body fat
It is calculated using the body composition analyzer "In Body 910" in dynamics (at the start and at the end of the trial).
Body Mass Index
BMI will be determined by the equation (kg/m2) in dynamics (at the start and at the end of the trial).
Waist circumference
Waist circumference will be measured on bare skin midway between the lowest rib and the superior border of the iliac crest using an inelastic measuring tape to the nearest 0.1 cm following the World Health Organization guideline. Measurement will be performed at the start and at the end of the trial.

Secondary Outcome Measures

Total Weight Loss
The difference in weight in kilograms compared to the baseline value after 6 months observation within the trial.
Percentage of Total Weight Loss
The ratio of the difference between the weight at the start of the trial and at the end of the trial in relation to the total body weight.
Eating behavior questionnaire
The investigators will analyse changes in eating behavior using the Food Frequency Questionnaire (FFQ) and the 24-hour replay method.
Hip circumference
Hip circumference will be taken on bare skin around the widest portion of the buttocks using an inelastic measuring tape to the nearest 0.1 cm and the tape should be placed parallel to the floor.
Waist circumference/Hip circumference
The ratio of the two values (Waist Circumference/Hip circumference) will be performed at the start and at the end of the trial.
Lean Mass
Lean mass will be simultaneously determined during the bioimpedance "In Body 910" scan for total body fat mass. Measurement will be performed at the start and at the end of the trial.
Health-related Quality of Life
The validated short form survey measures health-related quality of life covering physical functioning, emotional and mental health, bodily pain, general health, vitality, and social functioning. A higher overall score indicates better quality of life.
Adherence
Adherence will be verified by evaluating the completeness of the patient's diary.
Adverse Events
Adverse events will be closely monitored regularly by research personnel, and by subjects' voluntary reports.

Full Information

First Posted
January 28, 2022
Last Updated
September 27, 2022
Sponsor
National Medical Research Center for Therapy and Preventive Medicine
Collaborators
Moscow State University of Medicine and Dentistry
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1. Study Identification

Unique Protocol Identification Number
NCT05230628
Brief Title
Auricular Vagus Stimulation in Obesity
Official Title
The Effectiveness of Transcutaneous Electrical Nerve Stimulation of the Auricular Branch of the Vagus Nerve in Loss Weight and Improving the Quality of Life in Patients With Obesity
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 4, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Medical Research Center for Therapy and Preventive Medicine
Collaborators
Moscow State University of Medicine and Dentistry

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
Transcutaneous vagus nerve stimulation (TENS) involves stimulation of the left and/or right auricular branch of the vagus nerve with low-frequency electrical impulses. In recent years, the possibilities of using this technology in chronic conditions characterized by immune and metabolic dysregulation have been studied. The aim of this study is to investigate the effectiveness of TENS in reducing weight and improving quality of life in patients with various degrees of obesity.
Detailed Description
Obesity is one of the leading causes of disability and death worldwide. In 2016, more than 1.9 billion adults were overweight, according to the World Health Organization. According to current projections, by 2030, 60% of the world's population (that is, 3.3 billion people) may be overweight (2.2 billion) or obese (1.1 billion), if trends in obesity continue. In 2021, the journal Nature Communications published data on the effectiveness of the use of an invasive device that stimulates the efferent fibers of the vagus nerve of the stomach with light fluxes and thereby reduces the severity of hunger. In addition, in small clinical trials in patients with depression and epilepsy treated with transcutaneous vagus nerve stimulation, this procedure has been shown to lead to significant weight loss. Although the mechanisms are not fully understood, it is believed that a high-calorie diet contributes to the desensitization of the vagus afferent fibers to peripheral signals and leads to a decrease in the constitutive expression of orexigenic receptors and neuropeptides. Violation of signal transmission along the afferent fibers of the vagus nerve may be sufficient for the development of hyperphagia and obesity, and stimulation of the vagus nerve, respectively, can be used in the treatment of these conditions. Recent discoveries revealed a new and important role of the vagus nerve within a physiological mechanism that utilizes afferent and efferent signaling in controlling cytokine levels and inflammation - the inflammatory reflex. Afferent vagus nerve projections to the GI tract and the hepatic portal system play a major role in communicating alterations in peripheral metabolic homeostasis, including changes in cholecystokinin, lipids, leptin, insulin and glucose levels to the brain. In a reflex manner, efferent vagus nerve innervations of the heart, liver and pancreas provide cardio-metabolic regulatory output. Cholecystokinin- and leptin-induced afferent vagus nerve activity importantly mediates satiety and regulates feeding behavior. Cholecystokinin, released as a result of intestinal lipid accumulation also causes activation of afferent signaling and subsequent efferent vagus nerve output to liver that suppresses hepatic gluconeogenesis. Transcutaneous vagus nerve stimulation (TENS) involves the stimulation of the left and/or right auricular branch of the vagus nerve in the area of the cymba concha with low-frequency electrical impulses. The auricular branch of the vagus nerve runs superficially, which makes it a favorable target for non-invasive stimulation techniques to modulate vagal activity. It gained popularity due to minimal side effects and low cost. In recent years, the use of this technology in the treatment of various disorders, including headache, tinnitus, prosocial behavior, atrial fibrillation, associative memory, schizophrenia, traumatic pain, and Crohn's disease, has been explored - chronic conditions characterized by immune and metabolic dysregulation. For this reason, there have been many early-stage clinical trials on a diverse range of conditions. These trials often report conflicting results for the same indication. In this study, the investigators want to explore: will low-frequency transcutaneous electrical stimulation of the auricular branch of the vagus nerve contribute to weight loss in patients and improve their quality of life?

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vagus Nerve Stimulation, Obesity
Keywords
auricular stimulation, auricular vagus nerve stimulation, blinding (masking), transcutaneous vagus nerve stimulation (TENS), vagus nerve stimulation (VNS), obesity abdominal, nutrition disorders, overweight, body weight, active TENS, sham TENS, heart rate, total fat, body mass index, waist circumference, hip circumference, Heart rate variability, quality of life

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Model: 1:1 randomization of active stimulation vs. no stimulation for 6 months post randomization.
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Active TENS
Arm Type
Experimental
Arm Description
Active will be performed with using a TENS device with an ear clip attached to the tragus of the right ear (which is innervated by auricular branch of the vagus nerve) at 25 Hz, 200ms at a current just below discomfort threshold.
Arm Title
Sham TENS
Arm Type
Sham Comparator
Arm Description
Sham TENS will be performed to the ear lobe, which is devoid of vagal innervation.
Intervention Type
Device
Intervention Name(s)
Active TENS
Intervention Description
Active TENS stimulation will occur daily for 10 minutes, 3-4 times a day, 30 minutes before the main meals. The duration will be 6 months for each patient.
Intervention Type
Device
Intervention Name(s)
Sham TENS
Intervention Description
Sham TENS stimulation will occur daily for 10 minutes, 3-4 times a day, 30 minutes before the main meals. The duration will be 6 months for each patient.
Primary Outcome Measure Information:
Title
Percentage of body fat
Description
It is calculated using the body composition analyzer "In Body 910" in dynamics (at the start and at the end of the trial).
Time Frame
6-month follow-up
Title
Body Mass Index
Description
BMI will be determined by the equation (kg/m2) in dynamics (at the start and at the end of the trial).
Time Frame
6-month follow-up
Title
Waist circumference
Description
Waist circumference will be measured on bare skin midway between the lowest rib and the superior border of the iliac crest using an inelastic measuring tape to the nearest 0.1 cm following the World Health Organization guideline. Measurement will be performed at the start and at the end of the trial.
Time Frame
6-month follow-up
Secondary Outcome Measure Information:
Title
Total Weight Loss
Description
The difference in weight in kilograms compared to the baseline value after 6 months observation within the trial.
Time Frame
6-month follow-up
Title
Percentage of Total Weight Loss
Description
The ratio of the difference between the weight at the start of the trial and at the end of the trial in relation to the total body weight.
Time Frame
6-month follow-up
Title
Eating behavior questionnaire
Description
The investigators will analyse changes in eating behavior using the Food Frequency Questionnaire (FFQ) and the 24-hour replay method.
Time Frame
6-month follow-up
Title
Hip circumference
Description
Hip circumference will be taken on bare skin around the widest portion of the buttocks using an inelastic measuring tape to the nearest 0.1 cm and the tape should be placed parallel to the floor.
Time Frame
6-month follow-up
Title
Waist circumference/Hip circumference
Description
The ratio of the two values (Waist Circumference/Hip circumference) will be performed at the start and at the end of the trial.
Time Frame
6-month follow-up
Title
Lean Mass
Description
Lean mass will be simultaneously determined during the bioimpedance "In Body 910" scan for total body fat mass. Measurement will be performed at the start and at the end of the trial.
Time Frame
6-month follow-up
Title
Health-related Quality of Life
Description
The validated short form survey measures health-related quality of life covering physical functioning, emotional and mental health, bodily pain, general health, vitality, and social functioning. A higher overall score indicates better quality of life.
Time Frame
6-month follow-up
Title
Adherence
Description
Adherence will be verified by evaluating the completeness of the patient's diary.
Time Frame
6-month follow-up
Title
Adverse Events
Description
Adverse events will be closely monitored regularly by research personnel, and by subjects' voluntary reports.
Time Frame
6-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients with grade 1-2 nutritional obesity who are willing and able to give informed written consent to participate in the study, are on sinus rhythm and are not taking any antiarrhythmic drugs, including beta-blockers. Exclusion Criteria: Cardiac arrhythmias: bradyarrhythmias, Atrioventricular blockades of any degree; Taking beta blockers; The endocrine nature of obesity; Expected technical difficulties when using the device on the part of the patient; Pregnant or plan on becoming pregnant or breastfeeding during the study period; Presence of an electrically, magnetically or mechanically activated implant, an intracerebral vascular clip, or any other electrically sensitive support system.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Olga Dzhioeva
Phone
+7 (916) 614-18-21
Email
odzhioeva@gnicpm.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oxana Drapkina
Organizational Affiliation
National Medical Research Center for Therapy and Preventive Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Medical Research Center for Therapy and Preventive Medicine
City
Moscow
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Olga Dzhioeva
Phone
+79166141821
Email
odzhioeva@gnicpm.ru

12. IPD Sharing Statement

Citations:
PubMed Identifier
33420038
Citation
Kim WS, Hong S, Gamero M, Jeevakumar V, Smithhart CM, Price TJ, Palmiter RD, Campos C, Park SI. Organ-specific, multimodal, wireless optoelectronics for high-throughput phenotyping of peripheral neural pathways. Nat Commun. 2021 Jan 8;12(1):157. doi: 10.1038/s41467-020-20421-8.
Results Reference
background
PubMed Identifier
33994937
Citation
Verma N, Mudge JD, Kasole M, Chen RC, Blanz SL, Trevathan JK, Lovett EG, Williams JC, Ludwig KA. Auricular Vagus Neuromodulation-A Systematic Review on Quality of Evidence and Clinical Effects. Front Neurosci. 2021 Apr 30;15:664740. doi: 10.3389/fnins.2021.664740. eCollection 2021.
Results Reference
background
PubMed Identifier
32192678
Citation
Stavrakis S, Stoner JA, Humphrey MB, Morris L, Filiberti A, Reynolds JC, Elkholey K, Javed I, Twidale N, Riha P, Varahan S, Scherlag BJ, Jackman WM, Dasari TW, Po SS. TREAT AF (Transcutaneous Electrical Vagus Nerve Stimulation to Suppress Atrial Fibrillation): A Randomized Clinical Trial. JACC Clin Electrophysiol. 2020 Mar;6(3):282-291. doi: 10.1016/j.jacep.2019.11.008. Epub 2020 Jan 29.
Results Reference
background
PubMed Identifier
34473846
Citation
Wolf V, Kuhnel A, Teckentrup V, Koenig J, Kroemer NB. Does transcutaneous auricular vagus nerve stimulation affect vagally mediated heart rate variability? A living and interactive Bayesian meta-analysis. Psychophysiology. 2021 Nov;58(11):e13933. doi: 10.1111/psyp.13933. Epub 2021 Sep 2.
Results Reference
background
PubMed Identifier
32410932
Citation
Yap JYY, Keatch C, Lambert E, Woods W, Stoddart PR, Kameneva T. Critical Review of Transcutaneous Vagus Nerve Stimulation: Challenges for Translation to Clinical Practice. Front Neurosci. 2020 Apr 28;14:284. doi: 10.3389/fnins.2020.00284. eCollection 2020.
Results Reference
background

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Auricular Vagus Stimulation in Obesity

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