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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00218920
Other study ID # 4-2005.542
Secondary ID
Status Completed
Phase N/A
First received September 20, 2005
Last updated October 13, 2017
Start date September 2005
Est. completion date January 2008

Study information

Verified date October 2017
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim is to come to a consensus about how to prescribe exercise training that actually helps overweight and obese people. Thus, the present study determines the effects of several types of exercise training to define the one with the largest effect with the least effort.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 2008
Est. primary completion date January 2008
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Body mass index (BMI) over 30

Exclusion Criteria:

- Not able to walk on a treadmill

- Participating in an other study

- Serious cardiovascular diseases

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Strength training
a strength training regime of 4 series with 5 repetitions each, at approximately 90% of 1 repetition maximum (RM), in a leg press apparatus to develop maximal strength mainly from neural adaptation with minimal weight gain due to muscular hypertrophy.
continuous moderate-intensity aerobic training
The moderate-intensity group walked continuously for 47 min at 60-70% of maximum heart rate (HRmax) to ensure that the training protocols were isocaloric.
high-intensity interval aerobic training
High-intensity training consisted of a 10 min warm-up period at 50-60% of HRmax [maximal HR (heart rate)], followed by 4×4-min intervals at 85-95% of HRmax with 3 min active breaks in between the intervals, consisting of walking or jogging at 50-60% of HRmax. The exercise session was terminated by a 5 min cool-down period.

Locations

Country Name City State
Norway Norwegian University of Science and Technology Trondheim

Sponsors (1)

Lead Sponsor Collaborator
Norwegian University of Science and Technology

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Schjerve IE, Tyldum GA, Tjønna AE, Stølen T, Loennechen JP, Hansen HE, Haram PM, Heinrich G, Bye A, Najjar SM, Smith GL, Slørdahl SA, Kemi OJ, Wisløff U. Both aerobic endurance and strength training programmes improve cardiovascular health in obese adults — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Body weight 12 weeks
Primary Aerobic capacity 12 weeks
Primary Endothelial function 12 weeks
Secondary Molecular markers in fat and skeletal muscle biopsies for the effects of exercise training 12 weeks
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