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

Not Applicable
Not yet recruiting
Conditions
MeSH
Registration Number
NCT06520501
Lead Sponsor
Universitas Palangka Raya
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  1. Willing to be a respondent with informed consent
  2. Obesity sufferers in the Jekan Raya District area
  3. Have a BMI ≥ 25 kg/m2 (Obesity I)
  4. Adult age (19-39 years)
Exclusion Criteria
  1. Not being present or out of town during the research
  2. Unable to continue research due to serious illness or death
  3. Withdraw while participating in the research
  4. Have a history of drug allergies
  5. Experiencing decreased consciousness
  6. Experiencing an extremity injury
  7. Have a history of cardiovascular disease, kidney disease or stomach ulcers
  8. Have a history of bloody stools
  9. Are pregnant or breastfeeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Blood Glucose Differences7 consecutive day

Difference in blood glucose before and after treatment

Secondary Outcome Measures
NameTimeMethod

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