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Habitual Physical Activity clinical trials

View clinical trials related to Habitual Physical Activity.

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NCT ID: NCT03759951 Completed - Body Composition Clinical Trials

Hybrid Exercise Training for Health, Performance and Well-Being (DoIT II)

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

Observing a lack of research investigating the chronic physiological and psychological responses to this type of exercise training the aim of this study is to investigate the optimal training configurations of DoIT to produce positive effects on health, performance and quality of life markers in sedentary overweight or obese adults aged 30-55 years. The DoIT program will be performed in a small-group setting indoor or outdoor implementing a progressive manner for 12 months and using bodyweight exercises with alternative modes.

NCT ID: NCT03134781 Completed - Body Composition Clinical Trials

Hybrid Exercise Training for Weight Loss

DoIT
Start date: July 2015
Phase: N/A
Study type: Interventional

In this study the investigators utilized a novel hybrid HIIT (high intensity interval training) exercise training approach, the Hybrid Interval Training (DoIT) workout that combines interval training, resistance exercise training and functional training in order to test the hypothesis that DoIT will be able to: i) reduce body mass, ii) improve body composition and iii) alter energy balance, of previously inactive, overweight/obese women.

NCT ID: NCT01580930 Completed - Sedentary Time Clinical Trials

Changes in Habitual Physical Activity and Inactivity

START
Start date: March 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if individuals involved in exercise training change habitual activity and inactivity behavior outside of exercise training. Eligible participants were randomly assigned to one of four groups: control, exercise training, sedentary time reduction, or exercise training plus sedentary time reduction. It was hypothesized that participants in the exercise training group will compensate for exercise training by reducing free-living physical activity behavior and increasing sedentary time. Participant free-living behavior was monitored for one week at baseline, 3, 6, 9 and 12 weeks using an activPAL wearable monitor.