The Relationship Between Urinary Incontinence and Motor Symptoms

March 20, 2024 updated by: Pinar Yasar

The Relationship Between Urinary Incontinence and Motor Symptoms in Individuals With Stroke

There is no study in the literature examining the relationship between urinary incontinence and motor symptoms in individuals with stroke. The aim of this study is to determine the relationship between urinary incontinence and spasticity, balance and walking, which negatively affect quality of life and functional performance after stroke.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Evaluation parameters used in the study:

Modified Rankin Score 24 hours pad test Tinetti Balance and Gait Scale Modified Ashworth scale Danish Prostatic Symptom Score

Study Type

Observational

Enrollment (Actual)

46

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Isparta, Turkey
        • Suleyman Demirel University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

individuals with stroke

Description

Inclusion Criteria:

  • Being 18 years old, having a stroke history of at least 3 months, having had only one stroke, scoring between 0-2 points according to MRS, being able to stand and walk independently or with a walking aid, being able to speak Turkish.

Exclusion Criteria:

  • Those with incomprehensible speech disorders,
  • Those who have additional neurological diseases other than stroke,
  • orthopedic, cardiovascular, etc., which may cause balance disorders. those with illnesses,
  • those who are pregnant,
  • Those with vision and hearing loss

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
individuals with stroke
Diagnostic test: modified rankin scale

Modified Rankin Scale: The functional status of individuals with stroke is determined by this scale.

Modified Ashworth Scale: It allows determining the severity of spasticity. Tinetti Balance and Gait Scale: This scale helps determine the risk of falling by evaluating balance and gait.

Danish Prostatic Symptom Score: It allows to evaluate the storage and urinary functions of the bladder.

Other Names:
  • modified ashworth scale
  • Tinetti Balance and Gait Scale
  • Danish Prostatic Symptom Score

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
relationship with between urinary incontinence and motor symptoms
Time Frame: 4 months
correlation analysis was done.
4 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Pinar Yasar

Investigators

  • Study Director: Pinar Yasar, Suleyman Demirel University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2023

Primary Completion (Actual)

January 31, 2024

Study Completion (Actual)

February 15, 2024

Study Registration Dates

First Submitted

March 20, 2024

First Submitted That Met QC Criteria

March 20, 2024

First Posted (Actual)

March 27, 2024

Study Record Updates

Last Update Posted (Actual)

March 27, 2024

Last Update Submitted That Met QC Criteria

March 20, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 72867572-050.01.04-320

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

It was decided not to share the data, taking into account the personal data protection law.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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