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Auricular Stimulation for Relief of Stress and Anxiety (AA_COVID)

U

University Medicine Greifswald

Status

Unknown

Conditions

Stress and Anxiety

Treatments

Other: Auricular stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT04703907
BB 324/20

Details and patient eligibility

About

The aim of the study is to evaluate whether auricular stimulation (percutaneous sensory stimulation of cranial nerves) as compared vs. no intervention (waiting list) reduces stress and anxiety in health care providers, working at the time of COVID-19 pandemic at the University Medicine of Greifswald.

Enrollment

60 estimated patients

Sex

All

Ages

19 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Medical care workers at the University Medicine of Greifswald
  2. Experiencing stress and anxiety in connection with COVID-19 pandemic
  3. Participants without previous anxiolytic medication
  4. Ability to understand and fill in the structured questionnaire (Appendix D & E)
  5. Written informed consent

Exclusion criteria

  1. Recidivist alcoholics
  2. Local auricular skin infection
  3. Pregnant or lactating women
  4. Participants with prosthetic or damaged cardiac valves and mitral valve prolaps (risk of bacterial endocarditis according to guidelines of AHA)
  5. Participants who are unable to understand the consent form
  6. History of psychiatric disease

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Intervention group
Experimental group
Description:
This group is constituted from patients who will receive the intervention first within 15 weeks
Treatment:
Other: Auricular stimulation
Waiting list
No Intervention group
Description:
This group is constituted from patients who will receive the intervention after 15 weeks

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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