- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04472923
Biofeedback Training Fecal Incontinence in Children
Effect of Biofeedback Training on Functional Non-Retentive Fecal Incontinence in Children
Fecal incontinence (FI) is the inability to control bowel movements, causing stool to leak from rectum it ranges from an occasional leakage of stool while passing gas to a complete loss of bowel control after the age of 4 years1. Functional non-retentive fecal incontinence (FNRFI) is fecal incontinence in a child with a mental age of more than 4 years with no evidence of metabolic, inflammatory, or anatomical cause2.
The long-term result of biofeedback therapy is one of the most important subjects of controversy, and few studies have extended to 2 years of follow-up 11. So, the purpose of this study was to evaluate quantitatively the short-term and long-term efficacy of biofeedback training as a treatment tool designed to control functional non-retentive fecal incontinence in children and its long term impact on the quality of life.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Functional non-retentive fecal incontinence (FNRFI) is fecal incontinence in a child with a mental age of more than 4 years with no evidence of metabolic, inflammatory, or anatomical cause2.
It is an extremely embarrassing and psychologically frustrating shameful problem with a bad impact on children3. It can lead to social isolation, loss of self-confidence, depression, and behavioral problems4. The underlying mechanism of functional non-retentive fecal incontinence is largely unknown. The pathophysiology seems to be complex and it is considered to be a multifactorial disorder5. Approximately 95% of the children had no organic cause and these children are considered to have a functional defecation disorder. Of this, in approximately 80% of these children FI is results of constipation and is treated with laxatives, the remaining 20% without signs of fecal retention is classified as FNRFI6 The negative psychological and social impact for these children is high, however, and requires adequate intervention7. Biofeedback therapy is a feasible option that has been used for fecal incontinence over several decades8. The underlying premise of biofeedback, as with learning any physical activity, is that "practice makes perfect" if the learner is provided with accurate feedback to make adjustments to optimize performance So, the purpose of this study was to evaluate quantitatively the short-term and long-term efficacy of biofeedback training as a treatment tool designed to control functional non-retentive fecal incontinence in children and its long term impact on the quality of life.
Methods:
The present study included 100 children of both sexes that were included with an age ranged from (5-14 years) with FNRFI with normal bowel habits, normal defecation frequency, and normal stool consistency with incontinence score ranging from 6-24 according to Vaizey score 12. Exclusion criteria included; children who have traumatic sphincter injury, fecal impaction, spinal diseases causing incontinence, anorectal malformation, and children who were not cooperative. Patients included in this study were randomly divided and allocated into two groups Control group and Study group. Written informed consent was obtained from parents of all included children.
A detailed history was taken including bowel habits, duration history of trauma. Complete physical examination to exclude patients requiring surgical correction.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Al Qalyubia Governorate
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Banhā, Al Qalyubia Governorate, Egypt, 13511
- Benha University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age ranged from (5-14 years) with FNRFI with normal bowel habits
- Children with normal defecation frequency and normal stool consistency
- Children with incontinence score ranging from 6-24 according to Vaizey score
Exclusion Criteria:
- Children who have traumatic sphincter injury.
- Children who have Fecal impaction
- Children who have Spinal diseases causing incontinence
- Children who have Anorectal malformation
- Children who were not cooperative
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control group
Patients belonging to the control group received conventional physical therapy program in the form of diet and Kegel exercises.
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Patients belonging to the control group received conventional physical therapy program in the form of:
Other Names:
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|
Experimental: Study group
Patients belonging to the study group were subjected to the same conventional physical therapy program in addition to biofeedback training
|
Patients belonging to the study group were subjected to the same conventional physical therapy program in addition to biofeedback training. Biofeedback was planned after full guardians' education. Local hygiene for perianal skin for soiling episodes and using zinc oxide cream to prevent excoriation. Biofeedback was done using two types of catheters; a 24-channel water-perfused catheter with latex balloon for sensory training and a double-lumen rectal PVC balloon clothed catheter (MMS U-72210) for strength training. Each biofeedback session took 30 minutes with two sessions per week for 3 months. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of incontinence episodes
Time Frame: 24 months
|
Change in the number of incontinence episodes
|
24 months
|
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Incontinence Score using Vaizey incontinence score
Time Frame: 24 months
|
Questionnaire ranging from zero (indicating complete continence) to 24 (indicating total incontinence).
|
24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Fecal Incontinence Quality of life Score
Time Frame: 24 months
|
Change in quality of life score measured on a scale between 1 and 4, where 1 is very affected and 4 is not affected
|
24 months
|
|
Resting pressure (mm hg)
Time Frame: 3 months
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Pressure during relaxation of the anal sphincter
|
3 months
|
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Squeeze pressure (mm hg)
Time Frame: 3 months
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Pressure during contraction of the anal sphincter
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3 months
|
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First sensation (volume of the balloon by cm water)
Time Frame: 3 months
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First sensation of the stool in the rectum
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3 months
|
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First Urge (volume of the balloon by cm water)
Time Frame: 3 months
|
The patient is trying to hold defecation and he can
|
3 months
|
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Intense urge (volume of the balloon by cm water)
Time Frame: 3 months
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The Patent can no longer control the defecation
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3 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: Emad M Abdelrahman, M.D., Bnha University
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- BatterjeeMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- Study Protocol
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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