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临床试验/NCT06520501
NCT06520501尚未招募不适用

Comparison of the Effectiveness of Sambiloto Herbs (Andrographis Paniculata) and Brisk Walking Exercise on Blood Glucose of Obese Patients

Universitas Palangka Raya0 个研究点目标入组 30 人开始时间: 2024年7月21日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
30
主要终点
Blood Glucose Differences

研究概览

简要总结

Problem Formulation

  1. Does herbal medicine sambiloto affect the blood glucose levels of obese sufferers?
  2. Does brisk walking affect blood glucose levels in obese sufferers?
  3. Does the combination of bitter herbal medicine and brisk walking have an effect on blood glucose levels in obese sufferers?
  4. Is there a difference in the effectiveness between herbal bitter and brisk walking and the combination on blood glucose levels in obese sufferers?

Research Objectives

General Objectives :

The general aim of this research is to determine the difference in effectiveness between the herbal medicine Sambiloto and brisk walking as well as the combination on the blood glucose levels of obese sufferers.

Specific Objective :

  1. Knowing the effect of herbal medicine Sambiloto on blood glucose in obese sufferers.
  2. Knowing the effect of brisk walking on blood glucose in obese sufferers.
  3. To determine the effect of the combination of herbal medicine Sambiloto and brisk walking on blood glucose levels in obese sufferers.

详细描述

This type of research uses the Quasi Experimental method type Non-equivalent control group design, with a research design in the form of two group pre test and post test design, in this study there are two groups that will be measured pretest before intervention and post test after intervention and 1 control group without being given intervention. The intervention group is divided into two groups, namely the group given the herbal medicine sambiloto, and the group given the Brisk Walking Exercise treatment. Quasi-experimental research design with research design in the form of two group pre test and post test design.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
19 Years 至 39 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Willing to be a respondent with informed consent
  • Obesity sufferers in the Jekan Raya District area
  • Have a BMI ≥ 25 kg/m2 (Obesity I)
  • Adult age (19-39 years)

排除标准

  • Not being present or out of town during the research
  • Unable to continue research due to serious illness or death
  • Withdraw while participating in the research
  • Have a history of drug allergies
  • Experiencing decreased consciousness
  • Experiencing an extremity injury
  • Have a history of cardiovascular disease, kidney disease or stomach ulcers
  • Have a history of bloody stools
  • Are pregnant or breastfeeding

结局指标

主要结局

Blood Glucose Differences

时间窗: 7 consecutive day

Difference in blood glucose before and after treatment

次要结局

未报告次要终点

研究者

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

Agnes Veronica Agustin

Agnes Veronica Agustin

Universitas Palangka Raya

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