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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03440307
Other study ID # Cal Poly 11/12/2015
Secondary ID
Status Completed
Phase N/A
First received February 8, 2018
Last updated February 20, 2018
Start date November 12, 2015
Est. completion date November 11, 2017

Study information

Verified date February 2018
Source California Polytechnic State University-San Luis Obispo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date November 11, 2017
Est. primary completion date November 11, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Face-to-Face Meetings
Participants received health and fitness education, and a face-to-face 3-week intervention to reduce bisphenol exposure.
Email Only
Participants received health and fitness education.

Locations

Country Name City State
United States California Polytechnic State University San Luis Obispo California

Sponsors (1)

Lead Sponsor Collaborator
California Polytechnic State University-San Luis Obispo

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline Urine BPA at 3-weeks Change in urinary BPA measured at baseline and 3-weeks Single urine overnight fasted sample at baseline (date of randomization) and 3-weeks
Secondary Change from Baseline Urine BPS and BPF at 3-weeks Change in urinary BPS and BPF measured at baseline and 3-weeks Single urine overnight fasted sample at baseline (date of randomization) and 3-weeks
Secondary Change from Baseline Weight at 3-weeks Change in body weight measured at baseline and 3-weeks Overnight fasted weight at baseline (date of randomization) and 3-weeks
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