Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
FEMALE
Healthy Volunteers
NCT07554612

The Impact of Trunk and Lower Extremity Electrical Stimulation on Pelvic Floor Muscle Strength in Females

Led by Okan University · Updated on 2026-04-28

60

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the effects of whole-body electrical muscle stimulation (EMS) applied to the trunk and lower extremity muscles on pelvic floor muscle strength in healthy women. Since pelvic floor muscles are deep-seated and can be difficult to activate voluntarily, this research explores whether stimulating related muscle groups (core and legs) can provide an indirect benefit to pelvic floor strength. Participants will be divided into three groups (EMS + exercise, Sham-EMS + exercise, and exercise only) and will undergo a 6-week intervention program. Changes in pelvic floor muscle strength will be evaluated using a perineometer to determine the effectiveness of this non-invasive approach.

CONDITIONS

Official Title

The Impact of Trunk and Lower Extremity Electrical Stimulation on Pelvic Floor Muscle Strength in Females

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Biological female volunteers aged between 18 and 45 years.
  • Body Mass Index (BMI) between 18.5 and 29.9 kg/m².
  • Sedentary or low level of physical activity, no regular exercise in the last 6 months.
  • Volunteering and signing informed consent.
  • Mentally and physically able to follow the 12-week exercise and EMS protocol.
Not Eligible

You will not qualify if you...

  • History of pelvic floor or major abdominal surgery.
  • Pregnant or gave birth within the last 6 months.
  • Diagnosed neurological disorders affecting muscle control (e.g., Multiple Sclerosis, Parkinson's).
  • Active urinary tract infection or symptomatic pelvic organ prolapse.
  • Cardiac pacemaker or metal implants in trunk or hip area.
  • Chronic diseases interfering with exercise (e.g., uncontrolled hypertension, severe cardiovascular disease).
  • Skin lesions, infections, or severe sensitivity where EMS electrodes are applied.
  • Use of medications affecting muscle metabolism or neuromuscular system.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Istanbul Okan University Hospital

Istanbul, Istanbul, Turkey (Türkiye), 34959

Actively Recruiting

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Research Team

D

Dilara Taskiran, PT

CONTACT

A

Ahmet C Akgol, PhD, PT

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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