Plastic Detox During IVF Treatment
Endocrine Disrupting Chemical Detox: a Practical Method to Decrease Environmental Exposures and an Evaluation of the Impact on in Vitro Fertilization Treatment
Environmental pollutants are present in many aspects of everyday life. Exposures to common household products, such as food packaging and cookware, may affect reproductive health. Many of these environmental toxicants are known as "endocrine disrupting chemicals" because they can interfere with the body's hormone systems. Our study aims to create a guide that explains common sources of environmental toxicants and offer practical steps to reduce exposure. The investigators will evaluate how well participants understand this information and how consistently the intervention is maintained over time.
To assess whether these changes reduce environmental pollutant exposure, the investigators will measure levels of two classes of toxicants within the urine and blood at the beginning, middle and end of the study in patients struggling with infertility that are planning in vitro fertilization (IVF) treatment. The investigators will also measure the same chemicals in follicular fluid (fluid which surrounds developing eggs in the ovary) and seminal fluid (fluid which surrounds the sperm in semen) and compare these levels to samples from similar patients who did not receive the education or make environmental changes. The goal of this project is to determine whether simple changes to reduce exposure to environmental pollutants can lower chemical levels of toxicants in the body and whether this may ultimately impact outcomes for patients undergoing in vitro fertilization.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Abigail Mancuso, MD
- Número de teléfono: 319-356-1767
- Correo electrónico: abigail-mancuso@uiowa.edu
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
Descripción
Inclusion criteria:
- Unexplained infertility diagnosis (no identifiable male or female causes to infertility)
Exclusion criteria:
- Female age 38 years and older
- Male age 45 and older
- Diagnosis of diminished ovarian reserve
- Diagnosis of PCOS/PMOS
- Smoking or drug use in either male and/or female partner
- BMI >40 in either partner
- Patients using donor oocytes/donor sperm/donor embryos
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Plastic Detox
All participants recruited
|
All patients will be provided education on environmental pollutants and provide practical steps to reduce exposure.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Concentration of Bisphenol in urine
Periodo de tiempo: 12 weeks
|
Concentration of bisphenol will be measured in urine for each participant at 0, 6, and 12 weeks.
|
12 weeks
|
|
Concentration of PFAS in blood
Periodo de tiempo: 12 weeks
|
Concentration of PFAS will be measured in blood for each participant at 0, 6, and 12 weeks.
|
12 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Baseline environmental exposure questionnaire
Periodo de tiempo: 1 week
|
Participants will provide information to quantify their environmental exposures prior to the intervention in the form of a questionnaire.
Questions have been adapted from PACeQ (plastic associated chemicals exposure questionnaire) to assess exposure to diet/food preparation practices, physical environment, and personal care products.
The questionnaire will be delivered electronically.
|
1 week
|
|
Participant perception of educational material questionnaire
Periodo de tiempo: 1 week
|
Participants will assess the effectiveness of the educational material provided in the intervention.
Questionnaire adapted from the Patient Education Materials Assessment Tool (PEMAT).
|
1 week
|
|
Weekly Questionnaire to measure compliance with implementation strategies
Periodo de tiempo: 12 weeks
|
Participants in this study will choose implementation strategies to decrease their environmental exposure based on options provided in the education.
The participants will then provide a weekly summary of their compliance with their chosen implementation strategies in the form of a questionnaire administered electronically.
|
12 weeks
|
|
Concentration of bisphenol in follicular fluid and seminal fluid
Periodo de tiempo: 12 weeks
|
Participants follicular fluid and seminal fluid bisphenol concentration will be compared to a sample of previously banked control specimens.
|
12 weeks
|
|
Concentration of PFAS in follicular fluid and seminal fluid
Periodo de tiempo: 12 weeks
|
Participants follicular fluid and seminal fluid PFAS concentration will be compared to a sample of previously banked control specimens.
|
12 weeks
|
|
Seminal fluid analysis
Periodo de tiempo: 12 weeks
|
Semen sample will be analyzed prior to participants undergoing education on environmental toxins and methods to decrease exposure.
This baseline semen sample will then be compared to semen samples following the 12 week environmental pollutant detox.
Seminal fluid components that will be compared include concentration, motility, morphology, total motile sperm count.
|
12 weeks
|
|
IVF Outcomes
Periodo de tiempo: 45 weeks
|
Compare oocyte yield, fertilization rate, blastulation rate, clinical pregnancy rate, live birth rate to matched patients that did not undergo environmental pollutant detox.
|
45 weeks
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 202606064
- Environmental Fellows Award (Otro número de subvención/financiamiento: American Society for Reproductive Medicine)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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