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OpenTrials
Completed

NCT Number: NCT03653468

Exercise for Preventing the Metabolic Syndrome in Latinoamerican Amerindians

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).

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Key information

Conditions

Obesity Behavior Body Weight Cardiovascular Risk Factor Motor Activity Nutrition Disorders Nutritional and Metabolic Diseases Overnutrition Overweight Pathological Conditions, Signs and Symptoms Physical Activity Signs and Symptoms

Age range

30 year–59 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Cristian Alvarez

Los Lagos, Osorno, 000000000, Chile

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Concurrent training (CT)

Behavioral

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.

Primary outcomes

  1. Fasting glucose

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from Baseline in fasting glucose

  2. Total cholesterol

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from baseline in Total cholesterol

  3. Blood pressure

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from baseline in Blood pressure

Secondary outcomes

  1. Body mass

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from Baseline in body mass

  2. Waist circumference

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from Baseline in waist circumference

  3. Fat mass

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from Baseline in fat mass

  4. Lean mass

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from Baseline in lean mass

  5. Heart rate at rest

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from Baseline in heart rate at rest

  6. Six minutes walking test

    Time frame: Baseline and 20-weeks immediately after the interventions ends

    Change from Baseline in six minutes walking test

Sponsors and collaborators

Lead sponsor

Universidad Santo Tomas

Other

Collaborators

  • Healthcare Center Tomas Rojas
  • Universidad Pública de Navarra
  • Universidad de Los Lagos
  • Universidad del Rosario

Registry information

Official study title

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

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Aug 31, 2018
Registry last updated
Aug 31, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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