🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07562724
Starting soon Not applicable

Diet and WB-EMS Effects in Obesity

NCT07562724 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-09-01
Last updated
2026-05-14

Condition(s) studied

Obesity & OverweightMetabolic DisordersElectrotherapy

Investigational drug(s) / intervention(s)

Energy-Restricted DietWhole-Body Electromyostimulation (WB-EMS)

Energy-Restricted Diet: A personalized diet with approximately 750 kcal/day energy deficit.

Whole-Body Electromyostimulation (WB-EMS): Whole-body electromyostimulation applied 2-3 times per week for 8 weeks under supervision.

Study summary

Obesity is a major global health problem associated with metabolic dysfunction, altered adipokine signaling, and impaired appetite regulation. Conventional weight loss strategies such as calorie restriction often result in compensatory physiological adaptations, including increased appetite and loss of lean body mass, which may limit long-term effectiveness.

Whole-body electromyostimulation (WB-EMS) is an emerging, time-efficient intervention that induces simultaneous muscle activation and may improve metabolic health. However, the underlying molecular mechanisms, particularly the interaction between myokines and adipokines, remain insufficiently understood.

This randomized controlled trial aims to investigate the effects of an energy-restricted diet combined with WB-EMS on myokine-adipokine interaction, appetite regulation, and body composition in obese individuals. Participants will be randomly assigned to either a diet-only group or a diet plus WB-EMS group for 8 weeks.

Primary outcomes include changes in serum irisin levels. Secondary outcomes include myostatin, leptin, adiponectin, FGF-21, ghrelin, GLP-1, body composition parameters, and eating behavior. The findings of this study are expected to provide novel insights into the physiological and molecular effects of WB-EMS as a complementary strategy in obesity management.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Age between 18 and 65 years * Body mass index (BMI) ≥ 30 kg/m² * Sedentary lifestyle (less than 2 hours of structured exercise per week) * Willingness to participate and provide written informed consent Exclusion Criteria: * Presence of pacemaker or implantable cardioverter-defibrillator * Known cardiovascular disease or severe chronic illness * Pregnancy or breastfeeding * Uncontrolled diabetes or severe metabolic disorders * Active malignancy or cancer treatment * Severe renal or hepatic failure * Acute infection or inflammatory disease * Orthopedic conditions limiting physical activity * Use of medications affecting body composition or appetite (e.g., corticosteroids, weight-loss drugs) * Regular resistance training within the last 3 months * Substance abuse, including alcohol or drug dependency * Psychiatric or cognitive conditions affecting adherence to the study protocol

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Dicle University Diyarbakır Turkey (Türkiye)
Firat University Elâzığ Turkey (Türkiye)

More Firat University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07562724 on ClinicalTrials.gov ↗ ← All trials in Turkey