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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03300895 |
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Date of registration:
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28/09/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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High-intensity Interval Training on Cardiorespiratory Fitness in Overweight Women
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Scientific title:
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Effect of Low-volume High-intensity Interval Training on Cardiorespiratory Fitness and Total Body Fat in Overweight Women |
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Date of first enrolment:
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August 14, 2017 |
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Target sample size:
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35 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03300895 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Colombia
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Overweight (= 25 kg/m-2) women 18 to 44 years.
- Healthy volunteers.
- Perform = 600 Met/min/week.
Exclusion Criteria:
- Perform high-intensity interval exercise in the last six month.
- Smoker.
- History of asthma.
- History of diabetes.
- History of hypertension.
- History of cardiovascular disease.
- History of coronary heart disease.
- Arrhythmias.
- Personal history of surgical procedures in the last three months
- Uncontrolled non-communicable diseases
- Under medical treatment with anticoagulants, beta-blockers, calcium antagonists,
bronchodilators, and/or steroids.
- Psychological, neuromotor and/or osteo-muscular conditions that may affect
participation in an exercise program.
- Psychoactive drug abuse.
Age minimum:
18 Years
Age maximum:
44 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Healthy Volunteers
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Intervention(s)
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Other: High-intensity interval training
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Other: Comparator: Moderate-intensity continuous exercise
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Primary Outcome(s)
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Change in maximal oxygen consumption
[Time Frame: Baseline and after 10 weeks]
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Secondary Outcome(s)
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Change in total body fat
[Time Frame: Baseline and after 10 weeks]
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Secondary ID(s)
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HIIT2-AFIS-UdeA
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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