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High-intensity Intermittent Training for Obese Individuals

High-intensity Intermittent Training to Maximize Metabolic and Cardiovascular Protection in Obese Individuals

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01143376
Enrollment
46
Registered
2010-06-14
Start date
2010-05-31
Completion date
2014-01-31
Last updated
2017-04-20

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

Conditions

Obesity

Keywords

Obesity, exercise, body composition, insulin sensitivity, appetite, food intake

Brief summary

The most appropriate and effective exercise interventions for weight loss remain a matter of continued discussion and there is a need to identify sustainable exercise programs which successfully promote weight loss and benefit health. The primary objective of this study is to determine if high-intensity intermittent sprinting (HIIS) produces better results in terms of reducing metabolic and cardiovascular risk factors, with special emphasis to fat mass loss and insulin sensitivity in healthy obese volunteers compared with an iso-caloric program of moderate-intensity continuous cycling (MICC) (control condition following the international recommendations). We will also assess the impact of short duration sprints (SDS) in the above factors and to understand the potential mechanisms behind different outcomes among training programs. The overall hypothesis is that HIIS will lead to a greater reduction in metabolic and cardiovascular risk factors compared with MICC in healthy obese volunteers and that SDS will produce similar improvements in cardiovascular risk factors as the longer duration HIIS

Detailed description

Participants will be randomized to one of three groups: HIIS (8s sprint:12s rest) or MICC (control group) iso-caloric protocols (for the duration needed to induce a 250 kcal energy deficit) or SDS (8s sprint:12s rest) for 10 minutes for 12 weeks. The intervention groups will be matched for age, BMI and male/females ratio and participants will be asked not to change their normal diet throughout the study. Before and after the exercise intervention (12 weeks), participants will perform the following assessments: 1. Three-day food diaries 2. Anthropometric measurements (weight, height, waist and hips) using standard procedures; 3. Body composition using dual energy x-ray absorptiometry (DEXA) 4. RMR and resting respiratory exchange ratio (RER) using indirect calorimetry; 5. Endothelial function assessed by flow-mediated dilation (FMD) of the brachial artery using vascular ultrasound according to current guidelines; 6. Maximal oxygen uptake (VO2max) and fat oxidation, cardiac output and left ventricular function during exercise using a cycle ergometer; 7. Muscle and fat biopsies 8. Fasting and postprandial release of appetite related hormones (and subjective feelings of hunger/fullness using visual analogue scales - VAS).

Interventions

high-intensity intermittent sprinting (HIIS) (8 sec sprint:12 sec rest) for 12 weeks, 4 times a week

BEHAVIORALshort springs

short duration sprints (SDS)(8 sec sprint:12 sec rest) for 12 weeks, 4 times a week

Sponsors

Helse Midt-Norge
CollaboratorOTHER
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* weight stable on the last three months, * not currently dieting to lose weight * inactive lifestyle.

Exclusion criteria

* History of endocrine/cardiovascular/pulmonary/kidney disease, * anaemia, * gout, * depression or other psychological disorders, * eating disorders, * drug or alcohol abuse within the last two years * current medication known to affect appetite or induce weight loss. * planned surgery during the study period * participation in another research study * restraint score derived from the TFEQ\>12 * post-menopausal women

Design outcomes

Primary

MeasureTime frameDescription
Changes in body compositionBaseline and after 12 weeks of trainingBody composition assessed by DEXA

Secondary

MeasureTime frameDescription
Changes in insulin sensitivityBaseline and after 12 weeks of trainingInsulin will be measured in fasting and for 3h after a test meal

Countries

Norway

Outcome results

None listed

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