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Effects of Peripheral Magnetic Stimulation

Not Applicable
Completed
Conditions
Healthy
Interventions
Other: Exercise of the abdominal wall muscles
Device: Exercise with peripheral magnetic stimulation of the abdominal wall muscles
Registration Number
NCT05524636
Lead Sponsor
University of Primorska
Brief Summary

Interventional study of the effectiveness of peripheral magnetic stimulation of the abdominal wall muscles in healthy individuals.

Detailed Description

Interventional 8-week study of the effectiveness of peripheral magnetic stimulation of the abdominal wall muscles in healthy individuals. The study will include an experimental and a control group.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • healthy adults
  • BMI between 25,0 and 29,9 kg/m2
  • stable body mass with maximal variation of body mass of 2.2 kg a month prior to the inclusion in the study
  • waist circumference above 80 cm for females and above 90 cm for males
Exclusion Criteria
  • invasive fat reduction procedures (e.g., liposuction and mesotherapy)
  • weight loss supplements in the month prior to the participation in the study
  • metal implant
  • active implanted electrical device such as a cardiac pacemaker, cochlear implant, intrathecal pump, hearing aids, defibrillator, or drug delivery system

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ControlExercise of the abdominal wall musclesExercise without peripheral magnetic stimulation of the abdominal wall muscles
ExperimentalExercise with peripheral magnetic stimulation of the abdominal wall musclesExercise with peripheral magnetic stimulation of the abdominal wall muscles
Primary Outcome Measures
NameTimeMethod
Change in maximum isometric peak torqueBaseline, 4 weeks, 8 weeks, 12 weeks after baseline measurement

Maximal voluntary isometric contraction of the abdominal muscles. The measurement will be normalized to the body weight (Nm/kg).

Change in subcutaneous fatBaseline, 4 weeks, 8 weeks, 12 weeks after baseline measurement

Subcutaneous fat thickness in the abdominal area measured via ultrasound

Change in sitting postural controlBaseline, 4 weeks, 8 weeks, 12 weeks after baseline measurement

Sitting on an unstable surface for 30 seconds

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Primorska

🇸🇮

Izola, Primorska, Slovenia

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