NCT06842576

Brief Summary

The goal of this clinical trial is to assess whether social-media style short-form health education videos can increase health care transition readiness, self-efficacy, emotional well-being, health literacy, and appointment attendance, compared with publicly available health education resources in adolescents with chronic illnesses. The main question it aims to answer is:

  • Hypothesize social media intervention will increase health care transition readiness, self-efficacy, emotional well-being, health literacy, and appointment attendance compared to publicly available health education website immediately post intervention and at 6 month follow up. Participants will be randomly assigned to one of the interventions and access the intervention for 20 minutes and complete 30-60 minutes of surveys.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
44

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 19, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 24, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

June 1, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2026

Completed
Last Updated

May 2, 2025

Status Verified

April 1, 2025

Enrollment Period

9 months

First QC Date

February 19, 2025

Last Update Submit

April 29, 2025

Conditions

Keywords

mobile healthhealth educationtransition readinesschronic illnessadolescencehealth literacysocial mediavideoself efficacyemotional wellbeing

Outcome Measures

Primary Outcomes (5)

  • Self-reported score with a range from 1-5, on the Transition Readiness Assessment Questionnaire (TRAQ).

    The TRAQ assesses the readiness of youth and young adults to transition from pediatric to adult healthcare. It includes items related to managing medications, appointment keeping, tracking health issues, and communicating with healthcare providers.

    Immediate post-treatment and 6-month follow-up.

  • Self-reported score ranging from 1 to 4, via the Generalized Self-Efficacy Scale (GSES).

    The GSES evaluates an individual's belief in their ability to cope with a variety of difficult demands in life. It consists of 10 items, each rated on a 4-point scale, assessing confidence in handling unexpected events and solving problems.

    Immediate post-treatment and 6-month follow-up.

  • Self-reported score ranging from 1 to 5, via the Positive and Negative Affect Schedule for Children and Adolescents (PANAS-C).

    The PANAS-C measures positive and negative affect in children and adolescents. It includes items that assess the extent to which individuals experience various positive and negative emotions over the past few weeks.

    Immediate post-treatment and 6-month follow-up.

  • Self-report questionnaire with a score ranging from 10 to 40, via the Health Literacy for Youth.

    The HLSAC measures subjective health literacy in youth, focusing on their ability to access, understand, and use health information to make informed decisions.

    Immediate post-treatment and 6-month follow-up.

  • Number of appointments attended divided by the number of appointments scheduled, producing a score ranging from 0 to 100%, via medical chart abstraction.

    This measure calculates the percentage of scheduled medical appointments that were attended by the patient, providing insight into adherence to treatment plans and engagement with healthcare services.

    Comparing 6 months before intervention to 6 months after intervention.

Study Arms (2)

Health education videos

EXPERIMENTAL

The social media intervention will consist of 7 short videos between 20-60 seconds each, filmed by a professional videographer. Videos 1) start with text asking a question or giving a title highlighting the educational topic, 2) display adolescent volunteer patient partners directly teaching self-management and transition skills, demonstrating the skills via tutorials, or presenting health education content in the style of social media trends, and 3) conclude with a written summary of take-away points. The videos will be shared to participants as a password-protected Vimeo.com playlist. If participants are more comfortable in Spanish, they will be given the option to view the videos dubbed in Spanish.

Behavioral: Health Education Videos

Publicly Available Health Education Website

ACTIVE COMPARATOR

The social media intervention will be contrasted against a control condition consisting of sharing the GotTransition.org Youth and Young Adult Resources webpage: https://gottransition.org/youth-and-young-adults/. This website is a project from The National Alliance to Advance Adolescent Health. The webpage includes videos, infographics, quizzes, and frequently asked questions. Testing the social media intervention against this existing national resource will assess whether the novel intervention is relatively more acceptable or efficacious than an active comparison. If participants are more comfortable in Spanish, a prompt will be provided to them to use the website search function to locate resources in Spanish.

Behavioral: GotTransition.org Website

Interventions

Participants will be prompted to explore the 7 health education videos for up to 20 minutes.

Health education videos

Participants will be prompted to explore the Gottransition.org website for up to 20 minutes

Publicly Available Health Education Website

Eligibility Criteria

Age12 Years - 17 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

  • Patients in subspecialty clinics
  • Between 12 and 17 years old
  • With access to an internet-connected device
  • Speaking English or Spanish
  • With sufficient cognitive capacity to understand the study procedures, as assessed via a teach back method.

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Children Hospital Los Angeles

Los Angeles, California, 90027, United States

RECRUITING

Related Publications (3)

  • Carrera Diaz K, Yau J, Iverson E, Cuevas R, Porter C, Morales L, Tut M, Santiago A, Ghavami S, Reich E, Sayegh CS. Human-centered design approach to building a transition readiness mHealth intervention for early adolescents. J Pediatr Psychol. 2025 Jan 1;50(1):106-114. doi: 10.1093/jpepsy/jsae066.

    PMID: 39172486BACKGROUND
  • Bal MI, Sattoe JN, Roelofs PD, Bal R, van Staa A, Miedema HS. Exploring effectiveness and effective components of self-management interventions for young people with chronic physical conditions: A systematic review. Patient Educ Couns. 2016 Aug;99(8):1293-309. doi: 10.1016/j.pec.2016.02.012. Epub 2016 Mar 3.

    PMID: 26954345BACKGROUND
  • Modi AC, Pai AL, Hommel KA, Hood KK, Cortina S, Hilliard ME, Guilfoyle SM, Gray WN, Drotar D. Pediatric self-management: a framework for research, practice, and policy. Pediatrics. 2012 Feb;129(2):e473-85. doi: 10.1542/peds.2011-1635. Epub 2012 Jan 4.

    PMID: 22218838BACKGROUND

MeSH Terms

Conditions

Health EducationChronic Disease

Condition Hierarchy (Ancestors)

Adherence InterventionsMedication AdherencePatient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehaviorDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Caitlin S Sayegh, PhD

    Children's Hospital Los Angeles

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Caitlin S Sayegh, PhD

CONTACT

Courtney Porter, MPH

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: pilot parallel randomized controlled trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Staff/USC Faculty

Study Record Dates

First Submitted

February 19, 2025

First Posted

February 24, 2025

Study Start

June 1, 2025

Primary Completion

February 28, 2026

Study Completion

February 28, 2026

Last Updated

May 2, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

To protect patient confidentiality, we will not share data.

Locations