- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01524952
The Effect of Combined Thermal and Electrical Muscle Stimulation (cTEMS) on Obesity
The Effect of Combined Thermal and Electrical Muscle Stimulation (cTEMS) on Cardiorespiratory Fitness and Adipose Tissue in Obese Individuals
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.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
-
Bergen, Norge, 5009
- Haukeland University Hospital
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Active
cTEMS
|
cTEMS in three 60-minute sessions per week for 8 weeks
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Oxygen uptake
Tidsramme: Baseline and after 10 weeks
|
Baseline and after 10 weeks
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Lipolytic activity
Tidsramme: Baseline and after 10 weeks
|
Lipolytic activity in adipose tissue measured by microdialysis
|
Baseline and after 10 weeks
|
|
Gene expression in adipose tissue
Tidsramme: Baseline and after 10 weeks
|
Baseline and after 10 weeks
|
|
|
Body composition
Tidsramme: Baseline and after 10 weeks
|
Body composition by DEXA
|
Baseline and after 10 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Studiestol: Jan Erik Nordrehaug, PhD, University of Bergen
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2009/1273
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