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Public Policy Evaluation: the Case of the Green Prescription

Evaluating Public Policy: A Case Study of the Green Prescription POLVERT (Green Policy - Evaluation and Results)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07234617
Acronym
POLVERT
Enrollment
210
Registered
2025-11-18
Start date
2025-11-10
Completion date
2027-08-31
Last updated
2025-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy

Keywords

Pesticides, organic vegetables

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.

Interventions

BEHAVIORALConsumption of organic vegetables

Consumption of organic vegetables or non-organic for control group (according to their usual habits) for 2 weeks

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 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

Exclusion criteria

* 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)

Design outcomes

Primary

MeasureTime frameDescription
Change in urinary pesticide concentrations over the two-week study period in the intervention groupDay 0 and at 2 weeksMeasured as the difference in pesticide levels before and after the intervention
Difference in urinary pesticide concentrations between the two groupsDay 0 and at 2 weeksMeasured as the difference in pesticide levels in intervention vs. control groups

Countries

France

Contacts

Primary ContactVirginie COLLIN-BUND, MD
virginie.bund@chru-strasbourg.fr+33 3 88 12 63 41

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026