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临床试验/NCT07731568
NCT07731568招募中不适用

Efficacy and Underlying Mechanisms of Group Natural Psychotherapy for Anxiety Symptoms In Chinese University Students

Beijing HuiLongGuan Hospital1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2026年7月10日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
55
试验地点
1
主要终点
Generalized Anxiety Disorder Assessment (GAD-7)

研究概览

简要总结

The goal of this clinical trial is to learn if Natural Psychotherapy(NPT) works to treat anxiety symptoms in university students. It will also learn about the efficacy of Natural Psychotherapy in comparison to CBT.

The main questions are: Does online group Natural Psychotherapy lower the participants' anxiety symptoms? Is there any difference between NPT and CBT? Researchers will compare online group Natural Psychotherapy to online group Cognitive Behavioral Therapy(CBT) to see if Natural Psychotherapy works better to lower anxiety symptoms.

Participants will:

Attend online groupNPT or group CBT once a week for 4 weeks; Complete online questionnaires before the intervention, after the first week, after four weeks and after eight weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Voluntarily signed the informed consent form
  • Generalized Anxiety Disorder-7 (GAD-7) total score≥4
  • Aged 18-30 years, currently enrolled as an undergraduate or postgraduate student.

排除标准

  • Severe depression or high risk of suicide
  • History of substance abuse, drug dependence, or psychotic disorders
  • Severe neurological diseases, severe somatic illnesses, or other conditions unsuitable for physical labor or physical activities
  • History of electroconvulsive therapy (ECT) within the past 6 months, or currently undergoing other pharmacological or systematic psychological treatments.

结局指标

主要结局

Generalized Anxiety Disorder Assessment (GAD-7)

时间窗: Baseline, After 1 Week, After 4 weeks, After 8 weeks

The GAD-7 is a 7-item, self-reported Likert scale used to assess the severity of participants' anxiety symptoms over the past two weeks. Each item is scored from 0 (not at all) to 3 (nearly every day), yielding a total score ranging from 0 to 21, with higher scores indicating greater anxiety severity. The primary endpoint will evaluate the mean change in GAD-7 scores from baseline (Pre-intervention) to post-intervention (Week 4) to determine the efficacy of the intervention.

次要结局

  • Beck Depression Inventory(BDI)(Baseline, After 1 week, After 4 weeks, After 8 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xiang Yang Zhang

Professor

Beijing HuiLongGuan Hospital

研究点 (1)

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