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AcuTA: Acupuncture in Test Anxiety

Acupuncture Randomized Trial for Preventing Test Anxiety

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02142231
Acronym
AcuTA
Enrollment
25
Registered
2014-05-20
Start date
2014-04-30
Completion date
2014-06-30
Last updated
2015-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Experimental Setting (Trier Social Stress Test TSST), Test Anxiety

Keywords

acupuncture, test anxiety, neuroenhancer, placebo

Brief summary

Test anxiety is a well-known phenomenon in general population, but only few scientific advances have been made in order to fully understand and prevent this circumstance. The number of students which use neuro enhancement to improve their performance and to prevent test anxiety, is increasing. A US-survey estimated that almost 7% of students in US universities have used prescription stimulants against anxiety, and that on some campuses, up to 25% of students had used them in the past year. Acupuncture might act as an alternate. Several trials could demonstrate, that different forms of acupuncture could relieve symptoms of pre-exam anxiety syndrome significantly and that this therapy was highly safe. In special, the investigation of single point effects in test anxiety could be of general interest. The acupuncture point with the most convincing evidence up to date is Heart 7. Yet, its effectiveness has mainly been chosen in combination with other acupuncture points and not as single remedy in test anxiety. Therefore we establish a trial investigating the immediate needling effects at Heart 7 on the reduction of test anxiety. Therefore qe implemented a validated stress test, the Trier Social Stress Test TSST, which is known to provoke serious stress responses in healthy subjects. 24 medical students with test anxiety in there history will be randomised to two interventional groups (verum acupuncture and laser acupuncture), being treated and then pass this test. Main outcome is the increase of cortisol in saliva, which is the standardized measure of stress response used in this paradigm.

Interventions

DEVICEAcupuncture

Sterile Acupuncture Needles (Seirin (R) 0.15x0.2) will be used, Needles are inserted for approx. 0.5-1 cm until deqi response is elicited

DEVICELaser Acupuncture

Therefore a laser irradiation is faked, approaching a nonfunctioning laser pen, which has been deactivated by the manufacturer (3B Scientific GmbH, Hamburg, Germany). Only red light is emitted. To further emphasize the imaginary power of this sham procedure, visual and acoustic signals accompany the red light emission. Patients are treated at the same acupuncture points as in the acupuncture group for one minute without skin contact. The resting time after treatment is 18 minutes.

Sponsors

Ludwig-Maximilians - University of Munich
CollaboratorOTHER
Goethe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Test Anxiety in the clinical history * Male medical students 3rd to 5th year * Compliance * Age \> 18 years * Smoking cessation for 24 hours

Exclusion criteria

* Severe physical or psychical illness * Psychiatric record in medical history * Continuous uptake of antipsychiatric medication, tranquilizers or neuro-enhancers * Acupuncture treatment within the last 4 weeks * Hang-over * Drug consumption * Smoking (\> 5 cigarettes/ day)

Design outcomes

Primary

MeasureTime frameDescription
Cortisol in saliva8 timepoints (in minutes: -40;-10;+10;+20;+30;+40;+55;+70)Saliva samples will be obtained at above mentioned intervals for subsequent analysis of cortisol a in saliva. The stress model used in this trial is supposed to elevate cortisol in saliva 3-5 fold in controls.

Secondary

MeasureTime frameDescription
Test Anxiety on a Visual Analogue Scale4 timepoints (in minutes: -40;-10;+20;+55)Visual Analogue Scale (ranging 0 to 10, with 10 being most anxious)
Primary Appraisal Secondary Appraisal2 timepoints (-40 and +10 minutes)validated questionnaire
Multidimensional Mood State Questionnaire4 timepoints )in minutes: -40;-10;+10;+20)validated questionnaire
State Trait Anxiety Questionnaire3 timepoints (in minutes: -40;-10;+10)validated questionnaire
alpha amylase in saliva6 timepoints (in minutes: -40;-10;+10;+20;+30;+55)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026