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临床试验/CTRI/2025/11/097208
CTRI/2025/11/097208尚未招募不适用

Faesibility,Safety And Efficacy Of Steam Bath On Blood Glucose Levels In Patient With Type - 2 Diabetes Mellitus: A Randomized Controlled Trial.

Government Yoga and Naturopathy Medical College1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年12月25日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
1.Fasting Blood Glucose Level (FBGL)

研究概览

简要总结

A Randomized Controlled Trial design will be conducted involving 50 subjects. All the eligible subjects will be divided into 2 groups. The study group will undergo a steam bath for 20 minutes a day, 5 days in a week for 2 weeks, while the control group will undergo regular conventional management for 2 weeks. The assessments will be taken at three time points: at baseline (one day before the intervention), during assessment (after 1 week of intervention), and post (after 2 weeks of intervention).

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
40.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Subjects with known case of T2DM
  • Subjects on regular oral anti.
  • diabetic medications
  • Willingness to participate in study.

排除标准

  • Subjects under insulin therapy Subjects with complications of T2DM like Neuropathy, Retinopathy etc., Subjects with psychiatric illness.
  • Women with menstruation, Pregnancy.
  • Subjects with other systemic disorders like renal, cardiovascular disorders, General hydrotherapy contra-indication such as hydrophobia, hypersensitive skin, open cuts and wounds, recent surgeries and fractures.

结局指标

主要结局

1.Fasting Blood Glucose Level (FBGL)

时间窗: Fasting Blood Glucose Level (FBGL), Post Prandial Blood Glucose levels (PPBG) will be taken at baseline one day before the intervention, during assessment after 1 week of intervention, and post assessment after 2 weeks of intervention

2. Post Prandial Blood Glucose levels (PPBG)

时间窗: Fasting Blood Glucose Level (FBGL), Post Prandial Blood Glucose levels (PPBG) will be taken at baseline one day before the intervention, during assessment after 1 week of intervention, and post assessment after 2 weeks of intervention

次要结局

  • 1.Feasibilty(2.Safety)

研究者

发起方
Government Yoga and Naturopathy Medical College
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr A Prasanth

Government Yoga and Naturopathy Medical College and Hospital, Arumbakkam, Chennai

研究点 (1)

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