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临床试验/ISRCTN14169596
ISRCTN14169596进行中(未招募)Unknown

ature-based therapy for Metabolic Syndrome - Salzburg

Paracelsus Medical University0 个研究点目标入组 140 人开始时间: 2024年6月10日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
发起方
入组人数
140

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Individuals aged between 40 and 65 of any gender
  • 2. Individuals diagnosed with metabolic syndrome according to the NCEP ATP III criteria (NCEP, 2001)
  • 3. Sedentary lifestyle: Category 1 (low physical activity) of the International Physical Activity Questionnaire – Short Form (IPAQ-SF))
  • 4. Low nature users: Category 1, 2 und 3 of the Monitor of Engagement with the Natural Environment Survey (MENE) – question nature use” (Natural England, 2020)
  • 5. Smartphone users

排除标准

  • 1.Acute contraindications:
  • 1.1.Malignant hypertension
  • 2.Contraindications or differential diagnosis
  • 2.1.Severe respiratory or lung disease (COPD according to GOLD Standard 3 and 4, severe asthma, emphysema)
  • 2.2.Arteriosclerotic event (e.g. myocardial infarction) < 6 months ago
  • 2.3.Uncontrolled metabolic diseases (e.g. uncontrolled diabetes mellitus)
  • 2.4.insulin-dependent diabetes mellitus
  • 2.5.Diagnosis or treatment of a malignant tumors < 3 years in the past
  • 2.6.Orthopedic illnesses that do not allow participation in hikes
  • 3.Factors that prevent or hinder participation in the intervention program
  • 3.1.Alcohol abuse
  • 3.2.Pregnancy
  • 3.3.insufficient knowledge of German language (written and spoken)
  • 4.Factors that prevent self-management:
  • 4.1.Presence or indication of clinical depression (< 13 points WHO-5)
  • 4.2.Serious other untreated psychiatric illnesses (e.g. schizophrenia)
  • 5.Certain medication intake:
  • 5.1.Taking preparations for weight reduction
  • 6.Participation in another interventional study within the period of the clinical trial (t1-t4) and less than 4 weeks before the start of the trial (t1)
  • 7.Participation in therapeutic weight loss programs within the period of the clinical study (t1-t4) and less than 8 weeks before the start of the study (t1)

研究者

发起方
Paracelsus Medical University

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