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Vagus Stimulation in Female Long COVID Patients. (Vagus)

Primary Purpose

Vagus Nerve Diseases, Long COVID, Long Covid19

Status
Recruiting
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
transcutaneous electrical vagal neurostimulation
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vagus Nerve Diseases focused on measuring auricular transcutaneous electrical vagal nerve stimulation, TENS

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Female patients with Long COVID (history, physical examination, findings) age 18-70 years signed informed consent Exclusion Criteria: Hearing aid implants (cochlear implants) surgical transection of the vagus nerve Malignancies autoimmune diseases orthopedic diseases rheumatological diseases neurological diseases postoperative, fresh injuries to the ear febrile diseases inflammations psychiatric diseases pacemakers implanted cardioverter and defibrillators (ICDs) seizure disorders Meniere's disease negative experience with electrotherapy insufficient knowledge of the German language

Sites / Locations

  • Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University of ViennaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Experimental

Arm Label

Vagus Nerve Stimulation with 10 Hertz

Vagus Nerve Stimulation with 25 Hertz

Vagus Nerve Stimulation with 2 Hertz

Arm Description

Twelve weeks home therapy with transcutaneous electrical neurostimulation (TENSeco®, CE197, Schwa-Medico Gmbh), transcutaneous 2-channel nerve stimulator. Matching ear electrode 3 DTS. Stimulation frequency: 10 Hertz Intensity: sensitive threshold; clearly perceptible, but pleasant Form of stimulation: biphasic Duration: 30 min Position: left ear Frequency: daily, in the evening, when all daily activities are done

Twelve weeks home therapy with transcutaneous electrical neurostimulation (TENSeco®, CE197, Schwa-Medico Gmbh), transcutaneous 2-channel nerve stimulator. Matching ear electrode 3 DTS. Stimulation frequency: 25 Hertz Intensity: sensitive threshold; clearly perceptible, but pleasant Form of stimulation: biphasic Duration: 30 min Position: left ear Frequency: daily, in the evening, when all daily activities are done

Twelve weeks home therapy with transcutaneous electrical neurostimulation (TENSeco®, CE197, Schwa-Medico Gmbh), transcutaneous 2-channel nerve stimulator. Matching ear electrode 3 DTS. Stimulation frequency: 2 Hertz Intensity: sensitive threshold; clearly perceptible, but pleasant Form of stimulation: biphasic Duration: 30 min Position: left ear Frequency: daily, in the evening, when all daily activities are done

Outcomes

Primary Outcome Measures

Heart rate variability
20-minute documentation of the heart rate variability with a 24-hour-elektrocardiography

Secondary Outcome Measures

blood pressure and pulse
via Boso Medicus plus their mutiplication for the rate-pressure-product
Saliva cortisol
in the morning until the latest 10am
Questionnaire Brief Fatigue Inventory (BFI)
Fatigue evaluation
Questionnaire Short form (SF)-36
Health related quality of life evaluation
Questionnaire Borg-Scale
Dyspnea evaluation
Questionnaire Insomnia Severity Index (ISI)
Sleep evaluation
Post-COVID-19 Functional Status scale (PCFS)
Grade 0-4

Full Information

First Posted
June 20, 2023
Last Updated
June 23, 2023
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT05918965
Brief Title
Vagus Stimulation in Female Long COVID Patients.
Acronym
Vagus
Official Title
Effects of Transcutaneous Electrical Neurostimulation on Female Patients With Long COVID - a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 22, 2023 (Actual)
Primary Completion Date
March 1, 2025 (Anticipated)
Study Completion Date
March 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of the present pilot study is to investigate the acceptance, feasibility and implementation of the vagus nerv stimulation in Long COVID patients. Additionally, the effects on parameters of the autonomic nervous system as well as on symptoms of Long COVID will be described in a pre/post comparison. For this purpose, a total of 45 female Long COVID patients will participate in the randomized controlled pilot study. Patients will perform auricular vagus stimulation daily for 12 weeks. The patient collective will be randomized into three groups (A: 10 hertz, B: 25 hertz, C: 2 hertz=control group). If appropriate results are obtained, further adequately powered intervention studies are planned.
Detailed Description
Patients start on day 0, when the first assessment takes place. This consists of a medical diagnostic interview and sociodemographic, anthropometric, medical and functional data are collected (for a detailed description, see chapter 5. Statistics). Subsequently, the patients fill out the given questionnaires (paper/pencil version), which are then evaluated. Subsequently, the test persons are trained by a doctor how the electrical stimulation works with a demo device. Finally, the device is taken over by the company Schwa-Medico. The whole first assessment lasts about 2 hours and always takes place from 8 a.m. at constant room temperature (22-23 C°). The outcome parameters are recorded before the start of the vagus nerve stimulation (T0), during the treatment after 4 weeks (T0+4Wo) and after a total of 12 weeks (T0+12Wo) after the end of the therapy. Which assessments are collected at the different time points is listed in the biometry section. The assessments are performed by physicians of the Department of Physical Medicine, Rehabilitation and Occupational Medicine. All assessments take place at relatively the same time, at constant room temperature (22-23 C°). The patients have to appear fasting. T0: Medical history, examination, randomization, pre-tests, enrollment. T0+4Wo: Intermediate examination T0+12Wo: final examination, post-tests, return of device This pilot study investigates the acceptability, feasibility, and implementation of the VNS measure in Long COVID patients. In addition, effects on autonomic nervous system parameters (heart rate, blood pressure, rate pressure product, heart rate variability = HRV, cortisol in saliva), on symptoms fatigue, dyspnea as well as health-related quality of life (HRQOL) are described: Time points: T0, T0+4wk, T0+12wk. Parameters - collected at relatively the same time each day, at constant room temperature (22-23 C°): Documentation of blood pressure and pulse rate: by means of Boso Medicus (Bosch + Sohn GmbH u. Co. KG, Jungingen, Germany), calculation of the so-called "rate pressure-product" (syst. blood pressure x heart rate) Heart rate variability Salivary cortisol Fatigue: Brief Fatigue Inventory (BFI) Health-related quality of life (HRQOL): SF-36 (short form) questionnaire instrument Dyspnea: Modified Borg Scale Sleep: Insomnia Severity Index (ISI)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vagus Nerve Diseases, Long COVID, Long Covid19, Post-COVID-19 Syndrome, Post-COVID Syndrome, Post COVID-19 Condition, Post COVID Condition
Keywords
auricular transcutaneous electrical vagal nerve stimulation, TENS

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vagus Nerve Stimulation with 10 Hertz
Arm Type
Active Comparator
Arm Description
Twelve weeks home therapy with transcutaneous electrical neurostimulation (TENSeco®, CE197, Schwa-Medico Gmbh), transcutaneous 2-channel nerve stimulator. Matching ear electrode 3 DTS. Stimulation frequency: 10 Hertz Intensity: sensitive threshold; clearly perceptible, but pleasant Form of stimulation: biphasic Duration: 30 min Position: left ear Frequency: daily, in the evening, when all daily activities are done
Arm Title
Vagus Nerve Stimulation with 25 Hertz
Arm Type
Active Comparator
Arm Description
Twelve weeks home therapy with transcutaneous electrical neurostimulation (TENSeco®, CE197, Schwa-Medico Gmbh), transcutaneous 2-channel nerve stimulator. Matching ear electrode 3 DTS. Stimulation frequency: 25 Hertz Intensity: sensitive threshold; clearly perceptible, but pleasant Form of stimulation: biphasic Duration: 30 min Position: left ear Frequency: daily, in the evening, when all daily activities are done
Arm Title
Vagus Nerve Stimulation with 2 Hertz
Arm Type
Experimental
Arm Description
Twelve weeks home therapy with transcutaneous electrical neurostimulation (TENSeco®, CE197, Schwa-Medico Gmbh), transcutaneous 2-channel nerve stimulator. Matching ear electrode 3 DTS. Stimulation frequency: 2 Hertz Intensity: sensitive threshold; clearly perceptible, but pleasant Form of stimulation: biphasic Duration: 30 min Position: left ear Frequency: daily, in the evening, when all daily activities are done
Intervention Type
Device
Intervention Name(s)
transcutaneous electrical vagal neurostimulation
Intervention Description
daily for 12 weeks
Primary Outcome Measure Information:
Title
Heart rate variability
Description
20-minute documentation of the heart rate variability with a 24-hour-elektrocardiography
Time Frame
3 times for 12 weeks
Secondary Outcome Measure Information:
Title
blood pressure and pulse
Description
via Boso Medicus plus their mutiplication for the rate-pressure-product
Time Frame
3 times for 12 weeks
Title
Saliva cortisol
Description
in the morning until the latest 10am
Time Frame
3 times for 12 weeks
Title
Questionnaire Brief Fatigue Inventory (BFI)
Description
Fatigue evaluation
Time Frame
3 times for 12 weeks
Title
Questionnaire Short form (SF)-36
Description
Health related quality of life evaluation
Time Frame
3 times for 12 weeks
Title
Questionnaire Borg-Scale
Description
Dyspnea evaluation
Time Frame
3 times for 12 weeks
Title
Questionnaire Insomnia Severity Index (ISI)
Description
Sleep evaluation
Time Frame
3 times for 12 weeks
Title
Post-COVID-19 Functional Status scale (PCFS)
Description
Grade 0-4
Time Frame
3 times for 12 weeks

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
More women are affected by Long Covid, also the homogeneity is granted in a small study population.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female patients with Long COVID (history, physical examination, findings) age 18-70 years signed informed consent Exclusion Criteria: Hearing aid implants (cochlear implants) surgical transection of the vagus nerve Malignancies autoimmune diseases orthopedic diseases rheumatological diseases neurological diseases postoperative, fresh injuries to the ear febrile diseases inflammations psychiatric diseases pacemakers implanted cardioverter and defibrillators (ICDs) seizure disorders Meniere's disease negative experience with electrotherapy insufficient knowledge of the German language
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Veronika Helbich-Poschacher, M.D.
Phone
+4314040043300
Email
veronika.helbich-poschacher@meduniwien.ac.at
First Name & Middle Initial & Last Name or Official Title & Degree
Mohammad Keilani, M.D.
Phone
+4314040043300
Email
mohammad.keilani@meduniwien.ac.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard Crevenna, M.D.
Organizational Affiliation
PMR&O
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University of Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Veronika Helbich-Poschacher, M.D.
Phone
+4314040043300
Email
veronika.helbich-poschacher@meduniwien.ac.at

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33892403
Citation
Raveendran AV, Jayadevan R, Sashidharan S. Long COVID: An overview. Diabetes Metab Syndr. 2021 May-Jun;15(3):869-875. doi: 10.1016/j.dsx.2021.04.007. Epub 2021 Apr 20. Erratum In: Diabetes Metab Syndr. 2022 May;16(5):102504. Diabetes Metab Syndr. 2022 Dec;16(12):102660.
Results Reference
background
PubMed Identifier
33483331
Citation
Shah W, Hillman T, Playford ED, Hishmeh L. Managing the long term effects of covid-19: summary of NICE, SIGN, and RCGP rapid guideline. BMJ. 2021 Jan 22;372:n136. doi: 10.1136/bmj.n136. No abstract available. Erratum In: BMJ. 2022 Jan 19;376:o126.
Results Reference
background
PubMed Identifier
35726132
Citation
Sylvester SV, Rusu R, Chan B, Bellows M, O'Keefe C, Nicholson S. Sex differences in sequelae from COVID-19 infection and in long COVID syndrome: a review. Curr Med Res Opin. 2022 Aug;38(8):1391-1399. doi: 10.1080/03007995.2022.2081454. Epub 2022 Jun 20.
Results Reference
background
PubMed Identifier
33243837
Citation
Dani M, Dirksen A, Taraborrelli P, Torocastro M, Panagopoulos D, Sutton R, Lim PB. Autonomic dysfunction in 'long COVID': rationale, physiology and management strategies. Clin Med (Lond). 2021 Jan;21(1):e63-e67. doi: 10.7861/clinmed.2020-0896. Epub 2020 Nov 26.
Results Reference
background
PubMed Identifier
32458400
Citation
Fudim M, Qadri YJ, Ghadimi K, MacLeod DB, Molinger J, Piccini JP, Whittle J, Wischmeyer PE, Patel MR, Ulloa L. Implications for Neuromodulation Therapy to Control Inflammation and Related Organ Dysfunction in COVID-19. J Cardiovasc Transl Res. 2020 Dec;13(6):894-899. doi: 10.1007/s12265-020-10031-6. Epub 2020 May 26.
Results Reference
background

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Vagus Stimulation in Female Long COVID Patients.

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