Effectiveness of Pelvic Floor Muscle Rehabilitation Combined With Desmopressin in Children With Primary Monosymptomatic Nocturnal Enuresis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age7-13
SponsorBahçeşehir University

About this trial

The aim of this randomized controlled trial is to evaluate the effects of Structured Pelvic Floor Muscle Rehabilitation (SPFMR) in children with Primary Monosymptomatic Nocturnal Enuresis (PMNE) who are undergoing desmopressin asetat (DDAVP) treatment prescribed by a pediatric urologist. The study aims to investigate whether SPFMR can reduce the frequency and severity of enuresis episodes and whether it can also reduce relapse rates in the short- and long-term follow-up. The main questions the study seeks to answer are:

* Does SPFMR reduce the frequency and severity of enuresis episodes in children with PMNE? * Does SPFMR treatment reduce relapse rates in children with PMNE in the long term? Researchers will compare the group receiving SPFMR in addition to DDAVP treatment with a control group receiving only DDAVP treatment. This comparison will help evaluate the effect of SPFMR on the severity of enuresis episodes and relapse rates.

Participants will:

* Receive DDAVP treatment (SPFMR group and Control group) * Participate in SPFMR sessions ( SPFMR group) * Keep a diary of enuresis frequency and severity * Assess relapse during short- and long-term follow-up

The hypotheses of the study are:

H0: Adding SPFMR to desmopressin treatment for children with PMNE has no short-term effect on the severity of enuresis episodes.

H1: Adding SPFMR to desmopressin treatment for children with PMNE has a short-term effect on the severity of enuresis episodes.

H0: Adding SPFMR to desmopressin treatment for children with PMNE has no long-term effect on the severity of enuresis episodes.

H2: Adding SPFMR to desmopressin treatment for children with PMNE has a long-term effect on the severity of enuresis episodes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Being between 7 and 13 years old

Diagnosed with primary MNE by a pediatric urology department within the last 6 months

No urinary tract infection verified by laboratory tests

Ability to communicate in Turkish and absence of mental deficit

Disqualifiers

Presence of orthopedic conditions preventing evaluation

Anatomical anomalies in the urinary system

History of urinary system surgery

Neurological disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • Structured pelvic floor rehabilitation

    Other intervention

    The classic DDVAP therapy will be administered by the pediatric urologist. The classic urotherapy training recommended for enuresis will be provided by the physiotherapist. In addition, structured pelvic floor muscle rehabilitation (SPFMR) will be provided by the physiotherapist for 10 weeks. Each session is planned to last approximately 60 minutes. SPFMR will include multiple interventions combined. Below is information about the brief interventions. * Diaphragmatic Breathing Training * Pelvic Floor Training with Biofeedback * Core Stabilization Exercises * Squat Exercises * External Rotator Strengthing * Adductor Strengthing * Balance Training * Home Exercises

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Control Group (CG)No intervention 0 interventions
Group B: Structered Pelvic Floor Muscle Rehabilitation Group (SPFMRG)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The Nighttime Bedwetting Diary

The diary records dry and wet nights, the amount of bedwetting, bedtime, and wake-up time. The nighttime bedwetting diary will be completed one week before treatment initiation, during the treatment period (10 weeks), and throughout the follow-up phase for both groups. Data will be shared weekly with the researchers, either face-to-face or via phone (WhatsApp, email, etc.).

Time frame
baseline; 10th week after baseline; 12th week after baseline and 16th week after baseline

Secondary outcomes

1

Uroflowmetry Test

During the uroflowmetry evaluation, patients will be asked to urinate into a sensor-equipped uroflowmetry container (MMES ® brand) when they feel the urge to urinate. For children whose feet do not touch the ground, a stool will be used to ensure a proper toilet position. To minimize external factors affecting the urination pattern, it will be ensured that no one else is present in the uroflowmetry room except the patient. The parameters obtained from the measurement will be used to evaluate the voiding phase of the bladder. Flow rate will be recorded. Flow rate is the volume of urine per unit of time, typically expressed in milliliters per second (ml/s).

Time frame
baseline; 10th week after baseline; 12th week after baseline and 16th week after baseline
2

Post-Void Residual (PVR) Assessment

The Clarius® transabdominal ultrasound device will be used, and measurements will be performed from the suprapubic region. During the measurement, the patient will be positioned in a supine position with knees slightly flexed and supported with a towel beneath. The volume values calculated by the probe in the coronal and sagittal regions in mm³ will be automatically multiplied by the ultrasound system to calculate the residual urine volume in the bladder.

Time frame
baseline; 10th week after baseline; 12th week after baseline and 16th week after baseline
3

Bladder Diary

The diary will be maintained over a 48-hour period, recording daytime voiding frequency, voided volume, fluid types, and the amounts.

Time frame
baseline; 10th week after baseline; 12th week after baseline and 16th week after baseline
4

Pelvic Floor Muscle Activation Measurement

After proper placement of the electrodes, PFM activity will be measured using the NeuroTrac Myoplus4 Pro device. The CE certificate and registration of the device with the Ministry of Health are presented. Participants will be asked to perform 5 seconds of maximal contractions of their PFM ("work" phase EMG activity) followed by 5 seconds of relaxation ("rest" phase EMG activity), repeated in succession after resting. The device provides verbal commands of "work" for each contraction and "rest" for each relaxation. The measurement lasts for 55 seconds.

Time frame
baseline; 10th week after baseline; 12th week after baseline and 16th week after baseline

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Bahçeşehir University

Lead sponsor

Private Selcuk Sılay Pediatric Urology Clinic

Collaborator

Medipol Acıbadem Regional Hospital

Collaborator