Effect of Probiotics on Constipation and Weight in CP

ClinicalTrials.gov Study Record Example Title The Effect of Using Lactobacillus reuteri and Prebiotic-Containing Lactobacillus rhamnosus Strains on Constipation and Weight Gain in Children with Cerebral Palsy: A Prospective Randomized Controlled Study ________________________________________ Brief Summary This clinical trial aims to determine whether daily supplementation with Lactobacillus reuteri or a prebiotic-enriched Lactobacillus rhamnosus formula can improve constipation and weight gain in children with cerebral palsy (CP). Constipation is a common problem in children with CP due to impaired intestinal motility and disruption of the gut microbiota. The study will compare the effects and safety of two probiotic products over a 28-day period.

________________________________________ Detailed Description Cerebral palsy (CP) is a non-progressive neurodevelopmental disorder characterized by impairments in movement and posture. Gastrointestinal complications, particularly chronic constipation and inadequate weight gain, are frequently observed in this population and may significantly affect quality of life. Altered intestinal motility, limited physical activity, and gut microbiota dysbiosis are considered key contributors to bowel dysfunction in children with CP.

Probiotics have been proposed as a supportive therapeutic approach for gastrointestinal symptoms through modulation of intestinal microbiota, enhancement of barrier function, and regulation of bowel motility. Lactobacillus reuteri and Lactobacillus rhamnosus are among the most commonly studied probiotic strains with documented benefits in pediatric gastrointestinal disorders. The addition of prebiotics such as inulin may further enhance probiotic efficacy by promoting the growth of beneficial bacteria.

This prospective, randomized, double-blind, controlled study is designed to evaluate the effects of daily probiotic supplementation on bowel habits and growth parameters in children with cerebral palsy. Eligible participants are allocated to one of three parallel intervention arms and followed for a 28-day treatment period.

Clinical assessments are conducted at baseline and at the end of the intervention period. Anthropometric measurements are obtained using standardized techniques. Stool samples are collected for laboratory analysis, and stool consistency is evaluated using a validated scoring system. Caregivers maintain a daily stool diary to document bowel movement frequency and gastrointestinal symptoms throughout the study period.

The study evaluates changes in bowel function and growth-related parameters over time, as well as the safety and tolerability of the probiotic formulations. Adverse events and treatment adherence are monitored throughout follow-up. This study aims to provide evidence on whether probiotic supplementation represents a safe and effective supportive strategy for managing constipation and improving nutritional outcomes in children with cerebral palsy.

________________________________________ Study Type Interventional (Clinical Trial) Study Design

• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Double-blind (Participant, Investigator)
• Primary Purpose: Treatment ________________________________________ Estimated Enrollment (Insert total number, e.g., n = 90 participants)

Official Title The Effect of Using Lactobacillus reuteri and Prebiotic-Containing Lactobacillus rhamnosus Strains on Constipation and Weight Gain in Children with Cerebral Palsy: A Prospective Randomized Controlled Study ________________________________________ Arms and Interventions Arm 1: Lactobacillus reuteri Participants receive Lactobacillus reuteri daily for 28 days. Arm 2: Lactobacillus rhamnosus + Prebiotic (Inulin) Participants receive a probiotic containing Lactobacillus rhamnosus with prebiotic inulin daily for 28 days.

Arm 3: Control Group Participants receive standard dietary management for constipation.

________________________________________ Primary Outcome Measures

1. Change in defecation frequency [Time Frame: Baseline and Day 28]
2. Change in stool consistency (Bristol Stool Scale) [Time Frame: Baseline and Day 28] ________________________________________ Secondary Outcome Measures

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1. Change in body weight and BMI [Time Frame: Baseline and Day 28]
2. Stool pH level [Time Frame: Baseline and Day 28]
3. Caregiver-reported gastrointestinal symptoms [Time Frame: Throughout 28-day follow-up]

4. Incidence of adverse events [Time Frame: Throughout 28-day follow-up]

   ________________________________________ Eligibility Criteria

   Inclusion Criteria:

   • Children aged 2-18 years
   • Diagnosed with cerebral palsy (GMFCS levels III-V)
   • Chronic constipation meeting Rome IV criteria
   • Stable medical condition and able to take oral or enteral feeding

   Exclusion Criteria:

   • Degenerative neurological diseases
   • Congenital gastrointestinal malformations
   • Inflammatory bowel disease or metabolic disorders
   • Kidney failure
   • Antibiotic, probiotic, or prebiotic use within one month before enrollment
   • Poor adherence (\<95%) or hospitalization during study period ________________________________________ Study Start Date January 2023 Estimated Study Completion Date February 2025 ________________________________________ Location Ordu University Faculty of Medicine, Departments of Pediatric Surgery, Pediatrics, and Pediatric Neurology, Ordu University Training and Research Hospital, Ordu, Turkey

   Sponsors and Collaborators

   • Sponsor: Ordu University Faculty of Medicine, Department of Pediatric Surgery
   • Collaborators: Department of Pediatrics and Division of Pediatric Neurology
   • Product Support: Nestlé (Inulin-Enriched Lactobacillus rhamnosus formulation)