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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05069207
Other study ID # KirikkaleUniversity71
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 5, 2021
Est. completion date February 28, 2023

Study information

Verified date March 2022
Source Kirikkale University
Contact Sümeyra Kapucu, PT
Phone +905465457109
Email sumeyra.kapucu@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Urinary incontinence in children is defined as involuntary leakage of urine. Urinary incontinence is the most common urological complaint in children. Many factors are effective in urinary incontinence. Research on the effectiveness of the diaphragm in postural stabilization, which the investigators think is one of these factors, is limited. The aim of this study is to compare the effectiveness of diaphragmatic breathing in postural stabilization with healthy individuals and individuals with urinary incontinence. As a result, it has been revealed that one factor of urinary incontinence is due to the dysfunction of diaphragmatic breathing and will be a step to increase awareness on diaphragmatic breathing.


Description:

Urinary incontinence in children is defined as involuntary leakage of urine. Urinary incontinence is the most common urological complaint in children. Nocturnal incontinence is the most common chronic problem of childhood as well as allergic diseases. Frequency rates of 5-15% are reported in various sources, and in studies conducted with school children in our country, quite high rates of 20-30% are found. It is estimated that there are over 50 million children with urinary incontinence worldwide. There are many studies in the literature to determine the epidemiology and causes of urinary incontinence. In this study, it is aimed to evaluate diaphragmatic breathing in postural stabilization in children with urinary incontinence. In our study, Kırıkkale University Faculty of Medicine hospital; Individuals between the ages of 5 and 18 who were diagnosed with urinary incontinence and volunteered to participate in the study will be included in the study. The number of individuals will be determined according to the power analysis to be made. Individuals will be divided into 4 groups according to their diagnosis. Four groups with monosymptomatic enuresis, non-monosymptomatic enuresis, daytime urinary incontinence and healthy children as the control group will be included in the study. Before individuals; Demographic characteristics such as age, gender, height and weight will be questioned. Quality of Life in Children with Urinary Incontinence Scale (PIN-Q), which is the evaluation parameters of the children included in the study, Voiding Disorders Symptom Score (IBSS) to assess the severity of children's voiding disorder symptoms , Dynamic Neuromuscular stabilization (DNS) to evaluate the diaphragm in postural stabilization ; S-index (Inspiratory muscle strength), Maximum inspiratory pressure (MIP) and volume (Volume (V)) parameters will be evaluated with the POWER breathe K5 to evaluate. Hypotheses : H01: Diaphragmatic breathing is active in postural stabilization in children with monosymptomatic enuresis compared to healthy children. H02: Diaphragmatic respiration is active in postural stabilization in children with non-monosymptomatic enuresis compared to healthy children. H03: Diaphragmatic breathing is active in postural stabilization in children with daytime urinary incontinence compared to healthy children. H1: In children with monosymptomatic enuresis, diaphragmatic breathing is not active in postural stabilization compared to healthy children. H2: Non-monosymptomatic In postural stabilization in children with enuresis, diaphragmatic breathing is not active compared to healthy children. H3: Diaphragmatic breathing is not active in postural stabilization in children with daytime Urinary Incontinence compared to healthy children. One of our aims in this study is to realize the importance of the diaphragm.


Recruitment information / eligibility

Status Recruiting
Enrollment 52
Est. completion date February 28, 2023
Est. primary completion date December 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 18 Years
Eligibility Inclusion Criteria: - Being diagnosed with urinary incontinence - Being between the ages of 5 -18 - Accepting participation in the research, Exclusion Criteria: - • Less than 5 years old, - With spina bifida, - Having frequent urinary tract infections, - Having a neurological disease, - Having a concomitant chronic disease, - Cognitive affect, - Having mental retardation, - Having undergone orthopedic surgery before, - In addition to nocturnal incontinence, overactive bladder, delayed voiding, underactive bladder, dysfunctional voiding, bladder outlet obstruction, stress urinary incontinence, vaginal reflux, giggle incontinence, bladder neck dysfunction, neurogenic bladder, urgency - Those who do not agree to participate

Study Design


Related Conditions & MeSH terms


Intervention

Other:
POWER breathe K5
Maximum inspiratory pressure (MIP) and volume (Volume (V)) parameters will be evaluated with the POWER breathe K5 to evaluate

Locations

Country Name City State
Turkey Kirikkale University Faculty of Medicine Kirikkale

Sponsors (1)

Lead Sponsor Collaborator
Kirikkale University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of Life Scale in Children with Urinary Incontinence (PIN-Q) It consists of 20 questions. Children are asked to rate each question between 0 and 4 (0=no, 1=never, 2=sometimes, 3=often, 4=always). The total score of the scale ranges from 0 to 80 points. An increase in the total score means that the quality of life of the child is negatively affected. through study completion, an average of six months
Primary Voiding Disorders Symptom Score (IBSS) It measures the severity of children's voiding disorder symptoms. It consists of 14 questions in total. The 13 questions of the questionnaire evaluate symptoms related to daytime incontinence, symptoms related to nocturnal incontinence, frequency of urination in one day, presence of constipation and various urinary incontinence related symptoms. The 14th question evaluates the impact on quality of life in relation to these symptoms.The total score of the scale ranges from 0 to 35 points. An increase in the total score means that the severity of voiding disorders symptom severity increases. through study completion, an average of six months
Primary Dynamic Neuromuscular stabilization (DNS) In the DNS approach, the dual function of the diaphragm, namely respiratory and postural function, is evaluated. through study completion, an average of six months
Primary POWERbreathe K5 It is a respiratory muscle force measurement device. It is designed to match dynamic changes in respiratory muscle strength throughout the breath. S-index (Inspiratory muscle strength), will be evaluated. through study completion, an average of six months
Primary POWERbreathe K5 It is a respiratory muscle force measurement device. It is designed to match dynamic changes in respiratory muscle strength throughout the breath. Maximum inspiratory pressure (MIP) will be evaluated. through study completion, an average of six months
Primary POWERbreathe K5 It is a respiratory muscle force measurement device. It is designed to match dynamic changes in respiratory muscle strength throughout the breath. Volume (Volume (V)) will be evaluated. through study completion, an average of six months
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