- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06698133
Knowledge and Habits of Pregnant Teens (KnowTeens)
Knowledge and Habits of Pregnant Teens: Analyzing Nutritional Status, Weight and Infant Birth Weight
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This research study is to see if someone's ability to understand and use health information (health literacy) is linked to gaining a healthy amount of weight during pregnancy and having a baby with a healthy birth weight. The main question aims to answer if there is a positive correlation between increased health literacy, gestational weight gain, and adequate infant birth weight. We are conducting a prospective randomized trial involving 50 pregnant teenagers and their baby at a single institution. We will obtain study consent for 18 and 19 years old, and parental permission and assent for 13 -17 years old.
Control Group will complete the 20 questions health literacy during the first visit and after 8 weeks. Also, will complete the online called ASA 24 a 24-hour food recall tool. The ASA24 will be completed 2x /week for 8 weeks.
Intervention Group will complete the 20 questions health literacy during the first visit and after 8 weeks. Also, will complete the online called ASA 24 a 24-hour food recall tool. The ASA24 will be completed 2x /week for 8 weeks. In addition, participants assigned to the intervention group will be invited to participate in a private social media group. Participants will create a new account specifically for the study, or the study team can create an account on their behalf if they prefer. This will enable the study team to track participation without affecting any personal accounts. Education content will consist of published dietary recommendations during pregnancy, healthy craving hacks, healthy snacks, ways to get exercise in during the school day, etc. Participants will also be encouraged to ask questions and post any eating struggles.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Sheila Belk
- Phone Number: +1 (601) 984 -1690
- Email: sbelk@umc.edu
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Maternal age 13 - 19 yrs at enrollment
- < 19.6 gestational weeks
- Ability to understand English
- Access to a smartphone or internet
- Willingness to follow study procedures
- Plan to deliver at UMMC
- Singleton pregnancy
Exclusion Criteria:
- Does not meet the inclusion criteria
- History of diabetes
- Current record of substance abuse
- Mental impairment
- Eating disorder
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Arm
Control Group will complete the 20 questions health literacy during the first visit and after 8 weeks.
Also, will complete the online called ASA 24 a 24-hour food recall tool.
The ASA24 will be completed 2x /week for 8 weeks.
|
|
|
Experimental: Intervention Arm
Intervention Group will complete the 20 questions health literacy during the first visit and after 8 weeks. Also, will complete the online called ASA 24 a 24-hour food recall tool. The ASA24 will be completed 2x /week for 8 weeks. In addition, participants assigned to the intervention group will be invited to participate in a private social media group. Participants in the intervention arm will be invited to join a private social media group that will be created solely for this study. This will be a private account, accessible only to participants who are added or invited by the study team. |
Education content
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health Literacy
Time Frame: All study participants will complete this survey at the beginning of the study and again after week 8.
|
All data collected in the study design will be used to answer questions in this aim.
The Maternal Health Literacy (MaHeLi) is a 20-item questionnaire used to assess health literacy in adolescents .
|
All study participants will complete this survey at the beginning of the study and again after week 8.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Demographic Information
Time Frame: From enrollment to the end of 8 weeks
|
Demographic information will be collected, such as maternal age, gender, race, pre-pregnancy body mass index, weight, height, and BMI.
Obstetrical and medical history will also be collected but not limited to gestational age, historical and current maternal outcome.
Infant data will also be collected, such as gender, birth weight, infant unit admission, and infant outcome.
|
From enrollment to the end of 8 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
24-hour food recall tool
Time Frame: The ASA24 will be completed 2x /week for 8 weeks.
|
All study participants must complete the Automated Self-Administered 24-hour (ASA24) Dietary Assessment Tool to record dietary intakes.
The ASA24 dietary assessment tool is a web-based tool designed for collecting detailed dietary intake information.
ASA24 allows researchers and individuals to obtain dietary data through a 24-hour recall process, where participants report all the foods and beverages they consumed in the past 24 hours.
ASA24 uses a large database of foods, providing nutritional information like calories, macronutrients, vitamins and minerals.
|
The ASA24 will be completed 2x /week for 8 weeks.
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- UMMC IRB 2024-447
- Pending (Other Grant/Funding Number: Edwards Lifesciences Corp.)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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