跳至主要内容
临床试验/NCT05778994
NCT05778994
已完成
不适用

Use of the Intorus Device as a Therapeutic Tool for the Control of Anxiety Before the Exams in Occupational Therapy Students of the University of Extremadura

University of Extremadura1 个研究点 分布在 1 个国家目标入组 60 人2023年2月1日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
STUDENT
发起方
University of Extremadura
入组人数
60
试验地点
1
主要终点
Changes in the BECK anxiety questionnaire over 3 months
状态
已完成
最后更新
2年前

概览

简要总结

The goal of this clinical trial is to assess the possible efficacy of the INTORUS device as an element to reduce test anxiety in university students. The main question[s] it aims to answer are:

Can the INTORUS device be used as a tool to reduce anxiety? Once informed, those participants who meet the inclusion/exclusion criteria and sign the informed consent to participate in the study will be randomly divided into two groups. The randomization procedure will be carried out using the OxMaR (Oxford Minimization and Randomization) software.

All participants will be given the Sociodemographic Questionnaire, Self-efficacy Scale and anxiety questionnaire prior to the start of the study.

详细描述

The population is made up of students of the Degree in Occupational Therapy during the 2nd semester of the 2022-2023 academic year. The initial sample size will be approximately 70 participants. - Process Once informed, those participants who meet the inclusion/exclusion criteria and sign the informed consent to participate in the study will be randomly divided into two groups. The randomization procedure will be carried out using the Oxford Minimization and Randomization software. All participants will be given the Sociodemographic Questionnaire, Self-efficacy Scale and anxiety questionnaire prior to the start of the study. The participants of the experimental group will carry out a weekly exercise session with INTORUS aimed at reducing anxiety in the period between March 1, 2023 and May 10, 2023. On the day of the final exam for the subject, all students will repeat the anxiety measurement questionnaire and the perceived self-efficacy scale minutes before the final exam for the subject. Once the intervention period is over, a questionnaire will be passed to the professionals participating in the study to assess the usefulness of the device, the degree of satisfaction with it and the usefulness of the therapies applied.

注册库
clinicaltrials.gov
开始日期
2023年2月1日
结束日期
2023年7月31日
最后更新
2年前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
University of Extremadura
责任方
Principal Investigator
主要研究者

Blanca González Sanchez

DOCTOR. PRINCIPAL INVESTIGATOR

University of Extremadura

入排标准

入选标准

  • Students of the Degree in Occupational Therapy at the University of Extremadura.
  • Students who are going to study the Degree in Occupational Therapy in person.

排除标准

  • Not meeting the inclusion criteria
  • Not wanting to participate in the study

结局指标

主要结局

Changes in the BECK anxiety questionnaire over 3 months

时间窗: Measures before starting the intervention. through study completion, an average of 3 months.

Questionnaire to measure anxiety. The questionnaire consists of 21 questions, providing a range of scores between 0 and 63. The suggested cut-off points for interpreting the result obtained are as follows: 00-21 - Very low anxiety 22-35 - Moderate anxiety over 36 - Severe anxiety

次要结局

  • Changes in the questionnaire for the assessment of anxiety before exams(Measures before starting the intervention. through study completion, an average of 3 months.)
  • Changes in the Perceived self-efficacy scale in academic situations(Measures before starting the intervention. through study completion, an average of 3 months.)

研究点 (1)

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