Knowledge and Habits of Pregnant Teens

NCT ID: NCT06698133

Last Updated: 2025-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-04-01

Study Completion Date

2025-12-31

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Teen Pregnancy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants in the intervention arm will be invited to join a private social media group that will be created solely for this study. 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. The intervention will be completely virtual and outside of the initial visit. Medical advice will not be given; if requested, participants will be advised to contact their provider.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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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.

Group Type NO_INTERVENTION

No interventions assigned to this group

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.

Group Type EXPERIMENTAL

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

Intervention Type OTHER

Education content

Interventions

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

Education content

Intervention Type OTHER

Eligibility Criteria

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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

* History of diabetes
* Current record of substance abuse
* Mental impairment
* Eating disorder
Minimum Eligible Age

13 Years

Maximum Eligible Age

19 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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University of Mississippi Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Sheila Belk

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Sheila Belk

Role: CONTACT

+1 (601) 984 -1690

Other Identifiers

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pending

Identifier Type: OTHER

Identifier Source: secondary_id

UMMC IRB 2024-447

Identifier Type: -

Identifier Source: org_study_id

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