NCT07320573

Brief Summary

Pelvic floor muscle strength will be measured in women with stress urinary incontinence using superficial EMG, intravaginal EMG, and digital palpation. A 10-minute rest period will be given between each measurement, and the results will be recorded. Once all measurements are completed, any differences between the three measurements will be examined.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 21, 2025

Completed
4 days until next milestone

Study Start

First participant enrolled

December 25, 2025

Completed
12 days until next milestone

First Posted

Study publicly available on registry

January 6, 2026

Completed
19 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 25, 2026

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2026

Completed
Last Updated

September 22, 2026

Status Verified

September 1, 2026

Enrollment Period

1 month

First QC Date

December 21, 2025

Last Update Submit

September 21, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • pelvic floor muscle strength

    muscle strength and endurance durations

    day 1

Study Arms (1)

stress urinary incontinence

Pelvic floor muscle strength will be measured superficially, intravaginally, and digitally.

Device: Electromyography

Interventions

Muscle strength values will be obtained using surface electrodes.

stress urinary incontinence

Eligibility Criteria

Age18 Years - 70 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Women with stress urinary incontinence

You may qualify if:

  • Being over 18 years of age
  • Having stress urinary incontinence
  • Being willing to participate in the study

You may not qualify if:

  • Unwillingness to continue working
  • Presence of a neurological disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kirşehir Ahi Evran University Physical Therapy and Rehabilitation Hospital

Kırşehir, Centre, 40000, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Electromyography

Intervention Hierarchy (Ancestors)

ElectrodiagnosisDiagnostic Techniques and ProceduresDiagnosisMyography

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
LecTURER DOCTOR

Study Record Dates

First Submitted

December 21, 2025

First Posted

January 6, 2026

Study Start

December 25, 2025

Primary Completion

January 25, 2026

Study Completion

February 15, 2026

Last Updated

September 22, 2026

Record last verified: 2026-09

Locations