Prevention of maternal PKU syndrome: development and evaluation of a specific training seminar.

Not Applicable

• Conditions: E70.0; Classical phenylketonuria

• Registration Number: DRKS00032704
• Lead Sponsor: niversitätsklinik für Kinder- und Jugendmedizin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2022-07-09
• Study Start: 2023-09-26
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 21

Inclusion Criteria

Patients with PKU and their partners

Exclusion Criteria

Physical or mental impairment that makes participation impossible

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Knowledge level on maternal PKU measured by questionnaires with multiple-choice questions, measured right before the training and 4 months after.

Secondary Outcome Measures

Name	Time	Method
Quality of life measured by the validated BAI and BDI-II questionnaire.<br>Metabolic adjustment measured by Phe concentrations in the blood<br>Nutrient supply measured by eating diaries<br>Frequency of contact with PKU outpatient clinic