MedTrace Logo

Intervention to Reduce Bisphenol A Exposure in Women

NCT03440307 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2018-02-22

No results posted yet for this study

Summary

The purpose of this study is to determine whether a 3-week intervention reduces urinary Bisphenol A (BPA) in women with obesity

Conditions

  • Environmental Exposure

Interventions

BEHAVIORAL

Face-to-Face Meetings

Participants received health and fitness education, and a face-to-face 3-week intervention to reduce bisphenol exposure.

BEHAVIORAL

Email Only

Participants received health and fitness education.

Sponsors & Collaborators

  • California Polytechnic State University-San Luis Obispo

    lead OTHER

Principal Investigators

  • Debbie Hart · Compliance/Information Officer

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-11-12
Primary Completion
2017-11-11
Completion
2017-11-11

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03440307 on ClinicalTrials.gov