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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05524636
Other study ID # Fotona
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 15, 2022
Est. completion date July 20, 2022

Study information

Verified date August 2022
Source University of Primorska
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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 information / eligibility

Status Completed
Enrollment 40
Est. completion date July 20, 2022
Est. primary completion date July 20, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Device:
Exercise with peripheral magnetic stimulation of the abdominal wall muscles
8-week exercise program with peripheral magnetic stimulation, focused on abdominal wall muscles aiming to reduce subcutaneous fat, increase abdominal wall muscle strength and improve sitting postural control.
Other:
Exercise of the abdominal wall muscles
8-week exercise program focused on abdominal wall muscles aiming to reduce subcutaneous fat, increase abdominal wall muscle strength and improve sitting postural control.

Locations

Country Name City State
Slovenia University of Primorska Izola Primorska

Sponsors (2)

Lead Sponsor Collaborator
University of Primorska Fotona d.o.o.

Country where clinical trial is conducted

Slovenia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in subcutaneous fat Subcutaneous fat thickness in the abdominal area measured via ultrasound Baseline, 4 weeks, 8 weeks, 12 weeks after baseline measurement
Primary Change in maximum isometric peak torque Maximal voluntary isometric contraction of the abdominal muscles. The measurement will be normalized to the body weight (Nm/kg). Baseline, 4 weeks, 8 weeks, 12 weeks after baseline measurement
Primary Change in sitting postural control Sitting on an unstable surface for 30 seconds Baseline, 4 weeks, 8 weeks, 12 weeks after baseline measurement
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