Public Policy Evaluation: the Case of the Green Prescription
POLVERT
Evaluating Public Policy: A Case Study of the Green Prescription POLVERT (Green Policy - Evaluation and Results)
1 other identifier
interventional
210
1 country
1
Brief Summary
Numerous studies have highlighted the harmful effects of pesticide exposure during the prenatal period. Food is one of the main vectors of exposure to pesticides, particularly glyphosate, which is the most widely used herbicide. Observational studies have highlighted their effects on health, but few interventional studies have been conducted to identify effective interventions to reduce or eliminate environmental risks. In 2022, the City of Strasbourg implemented the "Ordonnance Verte" (Green Prescription) program, giving all pregnant women in the city access to a weekly basket of organic and local vegetables for several months, as well as awareness-raising workshops on endocrine disruptors and healthy eating. The objective of this study is to assess whether this type of program reduces pregnant women's exposure to pesticides compared to women who continue to eat according to their usual habits. If conclusive, this type of assessment would play a key role in facilitating the rollout of similar initiatives on a larger scale and protecting the health of pregnant women and future children.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable pregnancy
Started Nov 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 10, 2025
CompletedFirst Submitted
Initial submission to the registry
November 14, 2025
CompletedFirst Posted
Study publicly available on registry
November 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2027
November 19, 2025
November 1, 2025
1.7 years
November 14, 2025
November 18, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in urinary pesticide concentrations over the two-week study period in the intervention group
Measured as the difference in pesticide levels before and after the intervention
Day 0 and at 2 weeks
Difference in urinary pesticide concentrations between the two groups
Measured as the difference in pesticide levels in intervention vs. control groups
Day 0 and at 2 weeks
Study Arms (2)
Control
NO INTERVENTIONVegetable consumption according to habits
Intervention
EXPERIMENTALConsumption of organic vegetables
Interventions
Consumption of organic vegetables or non-organic for control group (according to their usual habits) for 2 weeks
Eligibility Criteria
You may qualify if:
- Be a woman
- Be less than 32 weeks pregnant
- Be registered with the "Ordonnance Verte" program
- Have agreed, when registering for the program, to be contacted by a research team
- Be affiliated with a social security system or be a beneficiary of such a system.
- Be fluent in French.
- Be over 18 years of age
- Be able to understand the objectives and risks associated with the research and give dated and signed informed consent
- Have a telephone and internet access
You may not qualify if:
- Participation in a study on nutrition or any other studies likely to affect exposure to the compounds under investigation
- Inability to provide informed consent (difficulties in understanding on the part of the pregnant woman, etc.)
- Being under judicial protection
- Being under guardianship or conservatorship
- Working in the agricultural sector (farmer, employee, apprentice)
- Living with someone who works in the agricultural sector (farmer, employee, apprentice)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hôpitaux Universitaires de Strasbourg
Strasbourg, 67000, France
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 14, 2025
First Posted
November 18, 2025
Study Start
November 10, 2025
Primary Completion (Estimated)
August 1, 2027
Study Completion (Estimated)
August 1, 2027
Last Updated
November 19, 2025
Record last verified: 2025-11
Data Sharing
- IPD Sharing
- Will not share