Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT07234617

Public Policy Evaluation: the Case of the Green Prescription

Led by University Hospital, Strasbourg, France · Updated on 2025-11-19

210

Participants Needed

1

Research Sites

89 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Public Policy Evaluation: the Case of the Green Prescription

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be a woman
  • Be less than 32 weeks pregnant
  • Be registered with the "Ordonnance Verte" program
  • Have agreed to be contacted by a research team when registering for the program
  • 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 study objectives and risks and provide dated and signed informed consent
  • Have telephone and internet access
Not Eligible

You will not qualify if you...

  • Participation in a nutrition study or any other study that may affect exposure to the compounds being investigated
  • Inability to give informed consent due to difficulties understanding
  • 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)

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hôpitaux Universitaires de Strasbourg

Strasbourg, France, 67000

Actively Recruiting

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Research Team

V

Virginie COLLIN-BUND, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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