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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01524952
Other study ID # 2009/1273
Secondary ID
Status Completed
Phase N/A
First received January 25, 2012
Last updated January 31, 2012
Start date December 2010
Est. completion date May 2011

Study information

Verified date January 2012
Source Haukeland University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway: Regional Ethics Commitee
Study type Interventional

Clinical Trial Summary

Objective:

It is unclear whether prolonged electrical muscle stimulation can improve cardiorespiratory fitness and reduce body fat in obese subjects. The purpose of this study is to investigate the effect of prolonged combined thermal and electrical muscle stimulation (cTEMS) on peak oxygen consumption (VO2 peak) and body composition. We will also investigate the biochemical effects and the resultant lipolysis-related gene expression changes in adipocytes.

Methods:Eleven obese (BMI≥30) individuals will receive cTEMS in three 60-minute sessions per week for 8 weeks. Activity levels and dietary habits will be kept unchanged and controlled with an accelerometer and nutritional questionnaire. Before and after the stimulation period, functional capacity are assessed by VO2 peak, and body composition was assessed by dual-energy X-ray absorptiometry and bioelectrical impedance analyses. Lipolytic activity will be determined in abdominal adipose tissue by 24 hours of microdialysis on a sedentary day, and adipose tissue biopsies will be taken for the gene expression analysis.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date May 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria:

- Obese (Body mass index; BMI = 30 kg/m2),

- sedentary subjects (< 20 minutes of exercise < 3 days per week).

- Other inclusion criteria were age between 30 and 70 years and

- the ability to undergo exercise testing.

Exclusion Criteria:

- Pacemaker or implanted defibrillator,

- regular medication,

- cardiovascular disease,

- pulmonary disease,

- extensive dermatological disease or other primary diseases;

- pregnant women;

- and individuals who abuse alcohol or drugs were excluded from the study

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
combined thermal and electrical muscle stimulation (cTEMS)
cTEMS in three 60-minute sessions per week for 8 weeks

Locations

Country Name City State
Norway Haukeland University Hospital Bergen

Sponsors (2)

Lead Sponsor Collaborator
Haukeland University Hospital University of Bergen

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oxygen uptake Baseline and after 10 weeks No
Secondary Lipolytic activity Lipolytic activity in adipose tissue measured by microdialysis Baseline and after 10 weeks No
Secondary Gene expression in adipose tissue Baseline and after 10 weeks No
Secondary Body composition Body composition by DEXA Baseline and after 10 weeks No
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