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AnxietyAA_EW_AnxiNCT03093584

Auricular Stimulation vs. Expressive Writing for Exam Anxiety

A study testing Auricular acupuncture and Expressive writing in people with Anxiety, run by University Medicine Greifswald.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Title of the study: Auricular acupuncture (AA) vs. expressive writing for pre-exam anxiety - a randomised crossover study Study period: 04 / 2014 - 07 / 2014 Principal Investigator: Prof. Dr. T. Read more about this study

Who is it for?
Ages 19 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Anxiety
What is being tested?
Auricular acupuncture and Expressive writing
Could I receive a placebo?
No, everyone receives an active treatment
How many people
37 participants
Where
No sites listed yet
Study dates
Apr 2014to Jul 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 19 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Medical students at the University of Greifswald
  • Going to take part in oral exams of human anatomy
  • Participants without previous anxiolytic medication
  • Ability to express the thoughts and emotions ("expressive writing")
  • Written informed consent

Who cannot join

  • Recidivist alcoholics
  • Local auricular skin infection
  • Pregnant or lactating women
  • Participants with prosthetic or damaged cardiac valves, intracardiac and intravascular shunts, hypertrophic cardiomyopathy and mitral valve prolaps (risk of bacterial endocarditis according to guidelines of AHA)
  • Participants who are unable to understand the consent form
  • History of psychiatric disease

About this study

Official title: Auricular Acupuncture (AA) vs. Expressive Writing in Treatment of Pre-exam Anxiety - Randomised Crossover Study in Medical Students

Title of the study: Auricular acupuncture (AA) vs. expressive writing for pre-exam anxiety - a randomised crossover study

Study period: 04 / 2014 - 07 / 2014

Read more

Principal Investigator: Prof. Dr. T. Usichenko Department of Anaesthesiology and Intensive Care Medicine University Medicine of Greifswald

Aim of the study: To investigate the anxiolytic effect of AA vs. expressive writing and vs. no intervention in students, passing the oral exams in anatomy at the University of Greifswald

Design: Prospective randomised crossover trial

Interventions: 1. AA using indwelling fixed needles, retained 24 h in situ 2. Expressive writing

Number of volunteers: N = 40

Healthy medical students at the University of Greifswald Participants of the anatomy exams in spring/summer 2014 Without previous anxiolytic, sedative and analgesic medication No pregnancy or lactating Informed consent

Outcome measures: Anxiety level Heart rate, blood pressure Salivary α-amylase

Conditions
Anxiety
Being tested
Auricular acupuncture, Expressive writing
Medical subject headings
Anxiety Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Auricular acupunctureDevice

    Auricular acupuncture with indwelling fixed auricular acupuncture needles

  • Expressive writingBehavioural

    Expressive writing is a standard psychological method in treatment of exam anxiety

Study groups in NCT03093584
Study groupRoleWhat they receive
Auricular stimulationActive comparatorAuricular acupuncture with indwelling fixed auricular acupuncture needles
Receives: Device: Auricular acupuncture
Expressive writingExperimentalExpressive writing - sharing the emotional expectations in front of forthcoming exam
Receives: Behavioral: Expressive writing
No interventionNo interventionNo intervention, just observation and monitoring of outcome measures

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Intensity of anxiety

    State-trait-Anxiety Inventory

    Measured: 2 days

Secondary outcomes (3)
  1. salivary alpha-amylase

    enzymatic activity of salivary alpha-amylase

    Measured: 1 day

  2. heart rate

    heart rate

    Measured: 1 day

  3. blood pressure

    blood pressure

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Mar 2017
  2. Study startApr 2014
  3. Primary completionJul 2014
  4. Study completionJul 2014

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
37 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03093584
Sponsor's protocol ID
BB 037/14
Acronym
AA_EW_Anxi
Status last verified
Mar 2017
First submitted
23 Mar 2017
Last updated
29 Mar 2017
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Auricular acupuncture and Expressive writing in people with Anxiety, run by University Medicine Greifswald.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Mar 2017. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Intensity of anxiety (time frame: 2 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Mar 2017.

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