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Completed

NCT Number: NCT03440307

Intervention to Reduce Bisphenol A Exposure in Women

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

Completed

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Key information

Conditions

Environmental Exposure

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

California Polytechnic State University

San Luis Obispo, California, 93405, United States

About this study

The purpose of this study is reduce BPA exposure in women. The intervention is rooted in social cognitive theory, and is applied to environmental health.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI >29.9
  • Age 18-50 years
  • Non-smoking
  • English speaking

Exclusion criteria

  • History of infertility
  • Type 2 or Type 1 diabetes
  • Cardiovascular disease, or any other metabolic disease/complication
  • History of major psychiatric illness, drug abuse, or unsafe dieting practices
  • History of bariatric surgery
  • Pregnant women or women expecting or trying to become pregnant
  • Participating in other studies

Treatment and study plan

Face-to-Face Meetings

Behavioral

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

Email only

Behavioral

Participants received health and fitness education.

Primary outcomes

  1. Change from Baseline Urine BPA at 3-weeks

    Time frame: Single urine overnight fasted sample at baseline (date of randomization) and 3-weeks

    Change in urinary BPA measured at baseline and 3-weeks

Secondary outcomes

  1. Change from Baseline Urine BPS and BPF at 3-weeks

    Time frame: Single urine overnight fasted sample at baseline (date of randomization) and 3-weeks

    Change in urinary BPS and BPF measured at baseline and 3-weeks

  2. Change from Baseline Weight at 3-weeks

    Time frame: Overnight fasted weight at baseline (date of randomization) and 3-weeks

    Change in body weight measured at baseline and 3-weeks

Sponsors and collaborators

Lead sponsor

California Polytechnic State University-San Luis Obispo

Other

Registry information

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Feb 22, 2018
Registry last updated
Feb 22, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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