Anxiety Clinical Trial
Official title:
Is Auriculotherapy Responsable for Improvements on Anxiety Students' Prior and After Examinations?
Verified date | October 2022 |
Source | Universidade do Porto |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
As the investigators have shown before, there was a tendency for a reduction of anxiety levels on university students after 30 minutes, with auriculotherapy treatment before examinations have started. However, the effect was effective and clinically significant after 48 hours comparing auriculotherapy with placebo and no treatment. In this sense, the investigators intend to perform a new study with a large sample and introduce a new hypothesis. So, this study aims to detect the clinical effect of two auriculotherapy techniques on the anxiety levels of university students.
Status | Completed |
Enrollment | 26 |
Est. completion date | December 3, 2021 |
Est. primary completion date | December 3, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - University students - Unfamiliar with auriculotherapy, - No psychological disorders measured through Brief Symptom Inventory scale. Exclusion Criteria: - Students having any neurological disease, cardiovascular disease, renal disease or any chronic disease, such as diabetes or hypertension. - Pregnants. - Under psychiatric medication. |
Country | Name | City | State |
---|---|---|---|
Portugal | ICBAS | Porto |
Lead Sponsor | Collaborator |
---|---|
Universidade do Porto | Escola Superior Saúde Santa Maria |
Portugal,
Vieira, A., Hinzmann, M., Silva, K., Santos, M., & Machado, J. (2018). Clinical effect of auricular acupuncture in anxiety levels of students prior to the exams: A randomized controlled trial. European Journal of Integrative Medicine, 20, 188-192. doi:https://doi.org/10.1016/j.eujim.2018.05.012
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change on Spielberger's State-Trait-Anxiety Inventory (STAI) | Was developed by Spielberger and colleagues in 1970, validated for the Portuguese population, with the aim of analyzing anxiety symptoms. STAI is an instrument for measuring the state and trait of anxiety, consisting of two auto-answer questionnaires, each consisting of 20 items. The score ranges from 20 to 80 points on both scales, where 20 to 35 points means not anxious, 36 to 50 points is considered little anxious; 51 to 65 points means moderately anxious; and finally, 66 to 80 points the participant is considered very anxious. | Change from baseline to after 8 and 24 hours. | |
Primary | Change on Salivary amylase (U/ml) | The method responds to both pancreatic and salivary amylase isoenzymes. Samples will be diluted prior to analysis and all measurements are going to be in compliance with the national legal requirements. | Change from baseline to after 16 hours. | |
Secondary | Change on Visual analogic scale (VAS) for anxiety | Consists of a horizontal or vertical line, 100 mm long, which has marked the classification "totally calm and relaxed" at one end and, at the other, the classification "Worst fear imaginable". The respondent should mark the point that represents the degree of intensity of his anxiety. The distance between the beginning of the line, which corresponds to zero and the marked location, is then measured in centimeters, thus obtaining a numerical classification. The scale is reliable and correlated with STAI-Y1 (p <0.0001) for the level of anxiety and was used on our previous study | Change from one week before baseline to after 8 and 24 hours. | |
Secondary | Change on quality of sleep | The participants will be asked about the quality of sleep during the night before as: 1-no change, 2-better or 3- worse than the quality of sleep during the previous week. | Change from one week before baseline to after 8 and 24 hours. | |
Secondary | Change on Blood Glucose levels | Cortisol acts on two distinct fronts that results in increased amounts of glucose in the bloodstream. It stimulates gluconeogenesis in the liver, and the glucose produced is released into the bloodstream and stored as glycogen. In addition, by potentiating the effects of epinephrine, it elevates glycogenolysis in the liver, thus releasing a large amount of glucose into the bloodstream within minutes. | Change from baseline to after 30 minutes and 24 hours. | |
Secondary | Test performance | After the exam, the test performance (pass or fail) will also be recorded. | one week after examinations | |
Secondary | Adverse effects | We will collect data related to auriculotherapy´ adverse effects (e.g, pain, presence of hematoma, vagal reaction, and infection), by replying the Adverse effect questionnaire after the procedure, as well as 1 week after completion of the experimental session. | up to one week after baseline |
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