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NCT Number: NCT06698133

Knowledge and Habits of Pregnant Teens

This study examines the link between health literacy, gestational weight gain, and infant birthweight in pregnant teenagers. A randomized trial of 50 participants will be conducted at the University of Mississippi Medical Center. Consent will be obtained from all participants. Both control and intervention groups will complete a 20 questions health literacy assessment at baseline and after eight weeks, along with the ASA24 dietary recall tool twice weekly. The intervention group will join a private social media group created solely for study purposes. This will be a private account, accessible only to participants who are added or invited by the study team.

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Key information

Age range

13 year–19 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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

Treatment and study plan

Participants in the intervention arm will be invited to join a private social media group

Other

Education content

Primary outcomes

  1. 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 .

Secondary outcomes

  1. 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.

Other outcomes

  1. 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

University of Mississippi Medical Center

Other

Registry information

Official study title

Knowledge and Habits of Pregnant Teens: Analyzing Nutritional Status, Weight and Infant Birth Weight

Acronym: KnowTeens

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Nov 20, 2024
Registry last updated
Apr 1, 2025

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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