- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06728540
Respiratory and Pelvic Floor Muscle Functions of Children With Lower Urinary Tract Dysfunction
Investigation of Physical Activity Levels, Respiratory and Pelvic Floor Muscle Functions of School-Age Children With Lower Urinary Tract Dysfunction
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
İzmir
-
Izmir, İzmir, Turkey (Türkiye), 35330
- Izmir University of Economics
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria in LUTD group:
- Diagnosed with LUTD,
- Nighttime enuresis at least twice a week for at least 3 consecutive months.
- Daytime enuresis at least once a month for at least 3 consecutive months.
- Girls aged 6-14,
- who consent to participate in the study with the consent of their mother and father or legal guardian (legal representative) will be included in the study.
Inclusion Criteria for healthy individuals in the study:
- Girls aged 6-14,
- who consent to participate in the study with the consent of their mother and father or legal guardian (legal representative) will be included in the study.
Exclusion Criteria:
- Children under 6 years of age,
- Anatomical changes in the urinary system,
- Spina bifida,
- History of active urinary tract infection,
- Neurological disease,
- An accompanying respiratory system disease (asthma and a history of frequent upper respiratory tract infections),
- Cognitive impairment,
- Mental retardation,
- Chronic kidney disease,
- Who have previously undergone orthopedic surgery will not be included in the study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Children with Lower Urinary Tract Dysfunction (Study Group)
Children included in the study will be evaluated only once.
The sociodemographic and clinical characteristics of the children participating in the study will be evaluated with the evaluation form, respiratory muscle strength with the RP Check brand electronic pressure measurement device, and body composition with the Tanita MC-580 brand bioelectrical impedance analyzer.
Pelvic floor muscle functions of children with LUTD will be evaluated with the 632 Myomed biofeedback device.
The survey questions and the evaluation form will be filled out by the parents.
|
The sociodemographic and clinical characteristics of the children participating in the study will be evaluated with an evaluation form, respiratory muscle strength with an RP Check brand electronic pressure measurement device, and body composition with a Tanita MC-580 brand bioelectrical impedance analyzer.
Pelvic floor muscle functions of children with LUTD will be evaluated with a 632 Myomed biofeedback device.
The survey questions and the evaluation form will be filled out by the parents.
|
|
Other: Healthy Children (Control Group)
Children included in the study will be evaluated only once.
The sociodemographic and clinical characteristics of the children participating in the study will be evaluated with the evaluation form, respiratory muscle strength with the RP Check brand electronic pressure measurement device, and body composition with the Tanita MC-580 brand bioelectrical impedance analyzer.
Pelvic floor muscle functions of children with LUTD will be evaluated with the 632 Myomed biofeedback device.
The survey questions and the evaluation form will be filled out by the parents.
|
The sociodemographic and clinical characteristics of the children participating in the study will be evaluated with an evaluation form, respiratory muscle strength with an RP Check brand electronic pressure measurement device, and body composition with a Tanita MC-580 brand bioelectrical impedance analyzer.
Pelvic floor muscle functions of children with LUTD will be evaluated with a 632 Myomed biofeedback device.
The survey questions and the evaluation form will be filled out by the parents.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Strength of Respiratory Muscle
Time Frame: baseline
|
To measure respiratory muscle strength, maximal inspiratory pressure (MIP or PImax) and maximal expiratory pressure (MEP or PEmax) measurements will be used with a non-invasive, RP Check brand electronic pressure measuring device.
|
baseline
|
|
Level of Physical Activity
Time Frame: baseline
|
Physical Activity Questionnaire for Children (PAQ-C):The physical activity levels of children will be assessed using the Physical Activity Questionnaire for Children (PAQ-C). The PAQ-C was developed in Canada to evaluate moderate to vigorous physical activity levels. It is based on the child's self-reported recall of the previous 7 days. The PAQ-C consists of 10 items, with 9 items used to calculate the activity score. The first question includes a list of 22 commonly performed activities. Responses to this question are evaluated on a 5-point scale (1 = never, 5 = 7 times or more). An average score is calculated, with higher scores indicating higher levels of physical activity. |
baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Voiding Disorders
Time Frame: baseline
|
Voiding Disorders Symptom Score (VOS):The severity of voiding dysfunction symptoms in children will be assessed using the Voiding Dysfunction Symptom Score.
This score was developed by Akbal et al. in 2005 and consists of 14 questions in total.
Thirteen of the questions evaluate symptoms related to daytime urinary incontinence, nighttime urinary incontinence, daily voiding frequency, the presence of constipation, and various symptoms associated with urinary incontinence.
The 14th question assesses the impact of these symptoms on quality of life.
The total score of the scale ranges from 0 to 35 points, with higher scores indicating increased severity of voiding dysfunction symptoms.
|
baseline
|
|
Bladder and Bowel Dysfunction
Time Frame: baseline
|
Bladder and Bowel Dysfunction Scale (BDS):The severity of children's bladder and bowel dysfunction symptoms will be assessed with the Bladder and Bowel Dysfunction Scale.
The MBDS was developed by Afshar et al. in 2009.
Bladder and bowel dysfunction symptoms are assessed and diagnosed with this scale.
Its Turkish validity and reliability were made by Kaya Narter et al. in 2017.
The scale consists of 14 questions.
The first 13 questions are specific to bladder and bowel dysfunction symptoms.
The last question questions the degree of difficulty of completing the survey.
Each question is a 5-point Likert type and the last question is not added to the scoring.
The total score varies between 0-52 and an increase in the score means an increase in symptom severity.
|
baseline
|
|
Functions of Pelvic Floor Muscle
Time Frame: baseline
|
After a brief informative training using visuals about pelvic floor muscles and their functions, the electrical activity of the pelvic floor muscles of children with LUTD will be measured with the 632 Myomed biofeedback device.
|
baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Urogenital Diseases
- Male Urogenital Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Pregnancy Complications
- Urological Manifestations
- Pathological Conditions, Signs and Symptoms
- Behavior
- Signs and Symptoms
- Lower Urinary Tract Symptoms
- Pelvic Floor Disorders
- Motor Activity
- Diagnostic Techniques and Procedures
- Diagnosis
- Circulatory and Respiratory Physiological Phenomena
- Respiration
- Respiratory Physiological Phenomena
- Physical Examination
- Vital Signs
- Respiratory Rate
Other Study ID Numbers
- SYY_İEU_3
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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