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Concurrent Training and Prediabetes Control

Concurrent Training and Prediabetes Comorbidities: An Analysis of Non-responders Using Clinical Cutoff Points

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03502304
Enrollment
28
Registered
2018-04-18
Start date
2017-06-10
Completion date
2018-04-09
Last updated
2018-05-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metabolic Disturbance

Keywords

Metabolic syndrome, Obesity

Brief 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).

Interventions

BEHAVIORALEndurance 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.

Sponsors

Universidad de Los Lagos
CollaboratorOTHER
Healthcare Center Tomas Rojas
CollaboratorOTHER
Universidad del Rosario
CollaboratorOTHER
Universidad Santo Tomas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Intervention model description

Behavioral

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 59 Years
Healthy volunteers
Yes

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, 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.

Design outcomes

Primary

MeasureTime frameDescription
Fasting glucoseBaseline and 20-weeks immediately after the interventions endsChange from Baseline in fasting glucose
LipoproteinsBaseline and 20-weeks immediately after the interventions endsChange from baseline in lipoproteins

Secondary

MeasureTime frameDescription
Fat massBaseline and 20-weeks immediately after the interventions endsChange from Baseline in fat mass
Lean massBaseline and 20-weeks immediately after the interventions endsChange from Baseline in lean mass
Body massBaseline and 20-weeks immediately after the interventions endsChange from Baseline in body mass
Six minutes walking testBaseline and 20-weeks immediately after the interventions endsChange from Baseline in six minutes walking test
Heart rate at restBaseline and 20-weeks immediately after the interventions endsChange from Baseline in heart rate at rest
Waist circumferenceBaseline and 20-weeks immediately after the interventions endsChange from Baseline in waist circumference

Countries

Chile

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026