FindTrial
Sign In

Clinical study on relief of pre-test anxiety syndrome with aurical acupressure

Clinical study on relief of pre-test anxiety syndrome with aurical acupressure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009173
Enrollment
Unknown
Registered
2016-09-08
Start date
2015-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Test anxiety

Interventions

All people:aurical acupressure

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1) Individuals suffered from mild, moderate or severe pre-test anxiety syndrome according to Sarason Test Anxiety Scale(TAS); 2) Individuals with consent form, TAS and questionnaire completed.

Exclusion criteria

Exclusion criteria: 1) Individuals suffering from secondary anxiety due to somatic disease(s) such as hyperthyroidism, hypertension, coronary heart disease; 2) Individuals suffering from heart disease(s), for instance, valvular heart disease, myocarditis, arrthymia. 3) Individuals with psychiatric history, or with current psychiatric treatments; 4) Individuals who are on medication modulating heartbeat.

Design outcomes

Primary

MeasureTime frame
Test Anxicty Scale, TAS;—

Secondary

MeasureTime frame
Self-Rating Anxiety Scale;Expectation and Treatment Credibility Scale;—

Countries

China

Contacts

Public ContactLU HUANYU

Guangdong Provincial Hospital of Chinese Medicine

sasangin@163.com+86 020-81887233

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026