Exercise for Preventing the Metabolic Syndrome in Latinoamerican Amerindians

Obesity Clinical Trial

Official title:

Similar Improvements in Cardiometabolic Risk Factors for Preventing the Metabolic Syndrome in Latinoamerican Amerindians After 12-weeks of Concurrent Training

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03653468
• Other study ID #: 28082018
• Status: Completed
• Phase: N/A
• Start date: January 1, 2018
• Est. completion date: August 25, 2018

Study information

• Verified date: August 2018
• Source: Universidad Santo Tomas
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Despite exercise training decrease blood fasting glicaemy in 'average' terms, there is a wide inter-individual variability after exercise training explored mainly in adults but not in adults with prediabetes comorbidities. Thus, is yet unknown the effects and influence of the concurrent training (CT) eliciting responders (R) and non-responders (NR) cases (i.e., percentage of subjects who experienced a non-change/worsened response after training in some metabolic outcomes).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: August 25, 2018
• Est. primary completion date: May 28, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 30 Years to 59 Years

Eligibility

Inclusion Criteria:

• Written informed consent

• Interested in improving health and fitness

Exclusion Criteria:

• Cardiovascular contraindications to exercise

• History of stroke, asthma or chronic obstructive pulmonary disease, muscle-skeletal disorders

• Smoking

• A compliance rate to the exercise program = 70% was required for the participants in the intervention group to be included in the statistical analyses.

Related Conditions & MeSH terms

• Cardiovascular Risk Factor
• Metabolic Syndrome X
• Obesity
• Physical Activity

Intervention

Behavioral:
• Concurrent training (CT)
The core part of each session included resistance training (RT) followed by aerobic training exercises (for 50 and 30 minutes, respectively) and was preceded and followed by a 5-minute warm-up and cool-down with callisthenic movements.

Locations

Country	Name	City	State
Chile	Cristian Alvarez	Los Lagos	Osorno

Sponsors (5)

Lead Sponsor	Collaborator
Universidad Santo Tomas	Healthcare Center Tomas Rojas, Universidad de Los Lagos, Universidad del Rosario, Universidad Pública de Navarra

Country where clinical trial is conducted

Chile, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Fasting glucose	Change from Baseline in fasting glucose	Baseline and 20-weeks immediately after the interventions ends
Primary	Total cholesterol	Change from baseline in Total cholesterol	Baseline and 20-weeks immediately after the interventions ends
Primary	Blood pressure	Change from baseline in Blood pressure	Baseline and 20-weeks immediately after the interventions ends
Secondary	Body mass	Change from Baseline in body mass	Baseline and 20-weeks immediately after the interventions ends
Secondary	Waist circumference	Change from Baseline in waist circumference	Baseline and 20-weeks immediately after the interventions ends
Secondary	Fat mass	Change from Baseline in fat mass	Baseline and 20-weeks immediately after the interventions ends
Secondary	Lean mass	Change from Baseline in lean mass	Baseline and 20-weeks immediately after the interventions ends
Secondary	Heart rate at rest	Change from Baseline in heart rate at rest	Baseline and 20-weeks immediately after the interventions ends
Secondary	Six minutes walking test	Change from Baseline in six minutes walking test	Baseline and 20-weeks immediately after the interventions ends