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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02125149
Other study ID # 202954
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date September 2, 2014
Est. completion date October 31, 2024

Study information

Verified date February 2024
Source Arkansas Children's Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to determine how a mother's health and physical activity may influence her child's growth and development.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 284
Est. completion date October 31, 2024
Est. primary completion date October 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - BMI >30 - >18 years of age - Singleton pregnancy - Less than 12 weeks gestation - Sedentary - Conceived without assisted fertility treatments - Cleared by physician to exercise Exclusion Criteria: - Women with pre-existing medical conditions as determined by the PI to affect the outcomes of interest - Women who are using recreational drugs, tobacco, or alcohol during pregnancy - Women with contraindications to exercise during pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise Intervention


Locations

Country Name City State
United States Tonja C Nolen Conway Arkansas

Sponsors (1)

Lead Sponsor Collaborator
Arkansas Children's Hospital Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Risk of obesity in infants and children Birth weight, body fat, and metabolism will be evaluated during the first 2 years of life. 2 years
Secondary Maternal insulin sensitivity Fasted blood samples will be analyzed to assess glucose and insulin. 9 months
Secondary Maternal inflammation Markers of inflammation will be investigated in fasted serum samples. 9 months
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