- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03108001
Glowing and Expecting Follow Up
December 18, 2023 updated by: Arkansas Children's Hospital Research Institute
This study will help us learn more about how a mother's health during pregnancy may influence her child's growth and development later in life.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This study will follow participants who participated in the Glowing and Expecting study.
514 people who are 5 to 14 years of age who agreed to be contacted for future studies will be part of this study.
Study Type
Observational
Enrollment (Estimated)
514
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Audrey Martinez, MS, RD, LD
- Phone Number: 501-364-3309
Study Contact Backup
- Name: Tonja C Nolen, BS
- Phone Number: 501-364-3309
- Email: acncstudies@archildrens.org
Study Locations
-
-
Arkansas
-
Little Rock, Arkansas, United States, 72202
- Recruiting
- Arkansas Children's Nutrition Center
-
Contact:
- Jill A Harsch, BS
- Phone Number: 501-364-3309
- Email: acncstudies@uams.edu
-
Contact:
- Ashton Adkison, BS
- Phone Number: 501-364-3309
- Email: acncstudies@archildrens.org
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
5 years to 14 years (Child)
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Former Glowing and Expecting study participants aged 5 to 14 years of age.
Description
Inclusion Criteria:
- Former Glowing and Expecting study participants aged 5 to 14 years of age
Exclusion Criteria:
- Participants who were dropped from the Glowing and Expecting studies.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Lean mothers
Participants that were in Glowing born from Lean mothers.
|
Overweight mothers
Participants that were in Glowing born from Overweight mothers.
|
Obese mothers
Participants that were in Glowing born from Obese mothers.
|
Exercise group mothers
Participants that were in Expecting born from mothers that were in the exercise group.
|
Non Exercise group mothers
Participants that were in Expecting born from mothers that were in the non- exercise group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Child's growth and development
Time Frame: up to age 14
|
Will be determined with body composition equipment (DXA and NMR)
|
up to age 14
|
Child's metabolism and physical activity
Time Frame: up to age 14
|
Will be determined with metabolic cart and fitness test equipment
|
up to age 14
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 27, 2017
Primary Completion (Estimated)
March 1, 2031
Study Completion (Estimated)
March 1, 2031
Study Registration Dates
First Submitted
April 5, 2017
First Submitted That Met QC Criteria
April 5, 2017
First Posted (Actual)
April 11, 2017
Study Record Updates
Last Update Posted (Actual)
December 20, 2023
Last Update Submitted That Met QC Criteria
December 18, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 206188
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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