Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
28 participants
INTERVENTIONAL
2017-06-10
2018-04-09
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Control group
No-exercise
Endurance training plus resistant training
CT in women with prediabetes and co-morbidities associated. Exercise will be performed at three sessions per week. Post statistical analyses will be including analyses by the 2 groups proposed. All sessions will be supervised by an exercise physiologist during 20-weeks.
Endurance training plus resistant training
To concurrent training (endurance training plus resistant training, RT) program will be use cycle ergometers adapted for obese adults (OXFORDTM, model BE2601, OXOFORD Inc, Santiago, Chile) were used. Prior to the CT intervention, all subjects were familiarized (during 3 sessions) with the training protocols. The CT intervention included 3 weekly sessions of both ET and RT. The core part of each session included RT followed by ET exercises (for 50 and 30 minutes, respectively) and was preceded and followed by a 5-minute warm-up and cool-down with callisthenic movements.
Endurance training plus resistant training
CT in women with prediabetes and co-morbidities associated. Exercise will be performed at three sessions per week. Post statistical analyses will be including analyses by the 2 groups proposed. All sessions will be supervised by an exercise physiologist during 20-weeks.
Interventions
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Endurance training plus resistant training
CT in women with prediabetes and co-morbidities associated. Exercise will be performed at three sessions per week. Post statistical analyses will be including analyses by the 2 groups proposed. All sessions will be supervised by an exercise physiologist during 20-weeks.
Eligibility Criteria
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Inclusion Criteria
* Interested in improving health and fitness.
Exclusion Criteria
* History of stroke, asthma or chronic obstructive pulmonary disease,
* Muscle-skeletal disorders, and
* 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.
30 Years
59 Years
FEMALE
Yes
Sponsors
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Universidad de Los Lagos
OTHER
Healthcare Center Tomas Rojas
OTHER
Universidad del Rosario
OTHER
Universidad Santo Tomas
OTHER
Responsible Party
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Principal Investigators
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Cristian Alvarez, PhD
Role: PRINCIPAL_INVESTIGATOR
Universidad de Los Lagos
Locations
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Cristian Alvarez
Los Lagos, Osorno, Chile
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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9042018
Identifier Type: -
Identifier Source: org_study_id