NCT06718842

Walking Program in Fatty Liver Children With Phenylketonuria

Walking Program in Fatty Liver Children With Phenylketonuria: Response of Liver Enzymes

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (estimated)
• Sponsor: Cairo University · Academic / Other
• Sex: All
• Age: 9 Years – 12 Years
• Healthy volunteers: Not accepted

Summary

phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. PKU is usually associated with many metabolic complication including non-alcoholic fatty liver

Detailed description

this study will include PKU children sufferers 9n=40) with non-alcoholic fatty liver to be randomly assigned to group I (n=20) that will perform walking program (online supervised free walking that will be applied daily for eight weeks) or group II (N=20) that will act as waitlisted children

Conditions

• Phenylketonurias
• Non Alcoholic Fatty Liver

Interventions

Type	Name	Description
BEHAVIORAL	walking free online supervised program	this Group I will include PKU children sufferers (n=20) with non-alcoholic fatty liver that will perform walking program (online supervised free walking that will be applied daily for eight weeks)

Timeline

• Start date: 2024-09-15
• Primary completion: 2025-01-30
• Completion: 2025-01-30
• First posted: 2024-12-05
• Last updated: 2024-12-05

Locations

1 site across 1 country: Egypt