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临床试验/NCT06107777
NCT06107777已完成不适用

The Efficacy of Pharmacopuncture on Inpatients With Psychological Stress Caused by Traffic Accidents: A Practical Randomized Control Pilot Study

Jaseng Medical Foundation2 个研究点 分布在 2 个国家目标入组 50 人开始时间: 2023年11月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
2
主要终点
Hospital Anxiety and Depression Scale(HADS)

研究概览

简要总结

This study is a double blind, randomized controlled trail. Condition/disease: Psychological Stress treatment Intervention:Pharmacopuncture

详细描述

"Pharmacopuncture is a treatment that combines 2 of the most frequented Korean medicine treatment methods - traditional acupuncture and herbal medicine - by injecting herbal medicine extract at acupoints.

This treatment is known to be an important part of Korean medicine treatment. However, there has been no specific value for the effect of this treatment.

Therefore, the investigators are going to conduct a practical randomized controlled trials to verify the efficacy and safety of Pharmacopuncture on Psychological Stress. From October 2023 to December 2024, the investigators are going to collect 50 inpatients who are suffering from Psychological Stress with the HADS-A(Hospital Anxiety and Depression Scale-anxiety) or HADS-D(Hospital Anxiety and Depression Scale-Depression) over 8 after injury by traffic accident(TA). For experimental group(n=25), the investigators will conduct Pharamacopuncture on 5 mandatory acupoints and 3 additional acupoints if needed durling the hospitalization and other Korean medical treatment. For control group(n=25), just Korean medical treatment except Pharamacopuncture on mandatory acupoints and additional acupoints will be conducted.

For these two groups, the investigators will compare Psychological stress intensity scale: Hospital Anxiety and Depression Scale (HADS), NRS of Anxiety, NRS of Depression, NRS of Physical pain, Sleeping disorder intensity scale: Korean version of the Insomnia Severity Index(ISI-K), subjective stress scale caused by traumatic events: Revised Version of the Impact of Event Scale of Korea(IES-R-K), EuroQol 5-Dimension (EQ-5D-5L) and Patient Global Impression of Change (PGIC)."

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
19 Years 至 69 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged 19-69 years on the date they sign the consent form.
  • Patients who are suffered by Psychological Stress that occurred within 3 days after traffic accident.
  • Patients who are hospitalized due to traffic accident.
  • Patients with HADS-A ≥ 8 or HADS-D ≥
  • Patients who provide consent to participate in the trial and return the informed consent form.

排除标准

  • Patients with progressive neurological deficit or with serious neurological symptoms.
  • Patients with a specific serious disease that may interfere with the interpretation of the therapeutic effects or results: malignancy, spondylitis, inflammatory spondylitis, etc.
  • Patients who are taking steroids, immunosuppressants, mental illness drugs, or other drugs that may affect the results of the study.
  • Patients with medical history of brain disease or surgery due to trauma.
  • Patients who are addicted by drug or alcohol within the year.
  • If acupuncture is inadequate or unsafe: patients with hemorrhagic, receiving anticoagulants, severe diabetes and cardiovascular disease.
  • Patients who are pregnant or planning to become pregnant
  • Patients who are participated in clinical trials other than observational studies without therapeutic intervention.
  • Patients who are difficult to complete the research participation agreement
  • Other patients whose participation in the trial is judged by a researcher to be problematic

结局指标

主要结局

Hospital Anxiety and Depression Scale(HADS)

时间窗: Screeing day (day 1), Baseline (day2), Discharge 1 day, 15 days after admission day, 2 months after admission day

Hospital Anxiety and Depression Scale aims to measure symptoms of anxiety and depression. It is a self-rating scale developed to assess psychological distress in non-psychiatric patients. The HADS consists of 14 questions and each question is scored on a 4-point Likert scale(0=no problems, 3=severe problems) The odd numbers ask anxiety(HADS-A) and even number ask Depression(HADS-D). HADS-A (or HADS-D) cut-off score is 8 or above.

次要结局

  • Numeric Rating Scale of Depression(NRS of Depression)(From baseline(Day2) up to Discharge 1 day, Discharge 1 day, 15 days after admission day, 2 months after admission day)
  • EuroQol 5-Dimension (EQ-5D)(Baseline(day2), Discharge 1 day, 15 days after admission day, 2 months after admission day)
  • Korean version of the Insomnia Severity Index(ISI-K)(Baseline (day2), Discharge 1 day, 15 days after admission day, 2 months after admission day)
  • Korean version of the Insomnia Severity Index(IES-R-K)(Baseline (day2), Discharge 1 day, 15 days after admission day, 2 months after admission day)
  • Numeric Rating Scale of Anxiety (NRS of Anxiety)(From baseline(Day2) up to Discharge 1 day, 15 days after admission day, 2 months after admission day)
  • Numeric Rating Scale of Physical pain(NRS of Physical pain)(From baseline(Day2) up to Discharge 1 day, Discharge 1 day, 15 days after admission day, 2 months after admission day)
  • Patient Global Impression of Change (PGIC)(Discharge 1 day, 15 days after admission day, 2 months after admission day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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