Influencing a Vegan Diet and the Intake of Dietary Supplements During Pregnancy and Childhood
Launched by WOLFGANG HUBER-SCHNEIDER · Oct 30, 2024
Trial Information
Current as of July 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring how a vegan diet affects pregnant women and young children, specifically looking at their use of dietary supplements. The researchers want to understand what factors influence vegan parents' choices about supplements, where they get their information, and whether they face challenges when giving these supplements to their children. The goal is to gather important insights that can help provide better information and support for those following a vegan lifestyle, especially during pregnancy and early childhood.
To participate in the study, you need to be an adult (18 years or older) who is either a vegan woman who has been pregnant, a parent feeding a child aged 0-5 a vegan diet, or a medical expert such as a doctor or dietitian familiar with vegan nutrition. Participants will fill out a survey to share their experiences and knowledge. The study is currently recruiting, and all participants must understand German to take part. This research aims to improve the nutritional support available for vegans, ensuring they have reliable information about maintaining a balanced diet and using dietary supplements.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- A. For vegans:
- • 1. Females/gender-diverse participants (ages 18 and over) who follow/followed a vegan diet during their pregnancy/pregnancies (If there is/was more than one pregnancy, at least during one of their pregnancies)
- • 2. Parents (females/males/gender-diverse - ages 18 and over) who feed/fed their child/children (If there is more than one child, at least one of them) a vegan diet within the age of 0-5 years
- • 3. Vegan mothers/gender-diverse participants (ages 18 and over) who breastfeed/breastfed their infant(s)/child(ren). Answering questions regarding their infant(s)/child(ren) up to an age of 5 years will be included
- • 4. Pregnant and breastfeeding women/gender diverse participants/parents (f/m/d) who make rare exceptions to their vegan diet and a vegan diet of their child(ren) - up to an age of 5 years. Inclusion in the survey depends on the frequency of exceptions → determined through questions/given answers within the survey. Participants that consume animal products maximum twice a month will be included - hence participants who do not make vegetarian or pescetarian exceptions more than twice a month will be included 5.Confirmation of the consent form and participant information ( online - addressing the subjects, purpose and process of the study, opportunities for discussion of further questions, duration of the questionnaire, who is conducting the study, possibility for further inquiries)
- B. For medical experts:
- • 1. Gynaecologists, paediatricians, general practitioners, pharmacists, dieticians with or without a consulting focus on vegans
- • 2. Confirmation of the participant information/written consent
- Exclusion Criteria:
- A. For vegans:
- • 1. Females/gender-diverse participants who change/changed their vegan diet (eat/ate a vegetarian or omnivorous diet) during their pregnancy/pregnancies
- • 2. Parents who do not feed/have never fed their children a vegan diet at least up to an age of 5 years (If vegan mothers followed a vegan diet during their pregnancy, exclusion only relates to questions concerning their children)
- • 3. No confirmation of the consent form and participant information (online) For the inclusion into the study at least one inclusion criteria (plus participant information) must be fulfilled. Exclusion (or not inclusion) will happen if only exclusion 3 is fulfilled. If only 1 or 2 is fulfilled - and 3 is not, participants will be included in the survey. All criteria will be proven by the study physician.
- B. For medical experts:
- • 1. Other medical specialists than mentioned in inclusion criteria
- • 2. No confirmation of the participant information/no written consent For the inclusion into the study all criteria must be fulfilled. Exclusion (or not inclusion) will happen if only one exclusion criteria is fulfilled. All criteria will be proven by the study physician.
- • All participants have do understand the German language in order to answer the questionnaire.
About Wolfgang Huber Schneider
Wolfgang Huber-Schneider is a distinguished clinical trial sponsor renowned for his commitment to advancing medical research and innovative therapies. With extensive expertise in clinical trial design and management, he focuses on facilitating the development of novel treatments across various therapeutic areas. His collaborative approach fosters partnerships with academic institutions, healthcare professionals, and regulatory bodies, ensuring rigorous adherence to ethical standards and regulatory compliance. Huber-Schneider’s dedication to improving patient outcomes through meticulously conducted clinical trials positions him as a key player in the landscape of medical research and development.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Vienna, , Austria
Patients applied
Trial Officials
Wolfgang Huber-Schneider
Principal Investigator
University of Vienna
Karl-Heinz Wagner
Study Director
University of Vienna
Ingrid Kiefer
Study Director
Austrian Agency for Health and Food Safety GmbH - AGES
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported