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NCT Number: NCT07383714

Nudging Parental Actions for Youth Suicide Prevention

The goal of the study is to determine effectiveness of a behaviorally informed text messaging intervention to help parents increase safety practices and reduce their teens' access to lethal means following a suicide-related emergency department visit.

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Key information

Age range

13 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Children's Medical Center

Dallas, Texas, 75287, United States

Location status: Recruiting

Location contact

Emine Rabia Ayvaci, MD

CONTACT

[email protected]

+16508040602

About this study

This study tests a text messaging program that helps parents keep their teens safe after a visit to the emergency department for suicidal thoughts or behavior. Adolescents face a higher risk of suicide after leaving the emergency department, and limiting access to lethal means such as firearms, medications, or other dangerous items can help prevent suicide. The investigators invite parents and their teens aged 12 to 17 who visit the emergency department at Children's Medical Center Dallas for suicide-related reasons to join the study. After enrolling, families will be randomly assigned to one of three groups. The first group receives usual care, which includes standard counseling about keeping teens safe in the emergency room and no study text messages. The second group receives direct text messages three times a week with reminders about safety reminders. The third group receives risk-framing text messages three times a week, which include safety reminders and information about suicide risk following an emergency room visit to motivate parents to take action. The study measures whether these text messages help parents follow safety recommendations at home. Parents and teens complete short surveys at the start of the study, six weeks later, and twelve weeks later. The study also tracks whether the teen returns to the emergency department or attempts suicide again. The study aims to determine if text messages can increase parental safety practices, reduce teens' access to lethal means, and prevent future suicide attempts. UT Southwestern Medical Center and Children's Health Dallas conduct the study. Messages are delivered through a secure, HIPAA-compliant virtual platform to ensure privacy.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Guardian must be able and willing to provide informed consent, and the participant must be able and willing to provide assent.
  • Parent and adolescent willingness and ability to participate in study procedures and complete assessments at baseline, 6 weeks, and 12 weeks.
  • Presentation to the ED for a suicide-related emergency, defined as suicidal ideation within the last 2 weeks or a suicide attempt within the past month.
  • Adolescents aged 12-17 years during the consent.
  • Access to a mobile phone with text messaging capability for the parent/legal guardian.
  • Ability to communicate in English.

Exclusion criteria

  • Absence of a legal guardian capable of providing consent.
  • Parents/legal guardians without access to a mobile phone with texting capability.
  • Inability to communicate in English.
  • Adolescents in state custody or under legal restrictions that prevent study participation.
  • Adolescents involved in the justice system in a manner that would interfere with study participation.
  • Adolescents with autism spectrum disorder or intellectual development disorder needing substantial or very substantial support

Treatment and study plan

Text-messaging for safety reminders

Other

The intervention consists of thrice-weekly, behaviorally informed text messages delivered to parents over six weeks period.

Text-messaging with safety reminders and risk framing

Other

Thrice-weekly messages incorporating safety precautions and evidence-based suicide risk statistics to recalibrate parental risk perception.

Primary outcomes

  1. Parent-reported adherence to lethal means restriction (LMR)

    Time frame: Baseline to 6 weeks

    Change in parental adherence to lethal means restriction practices will be assessed using the Parent Adherence to Lethal Means Restriction (PA-LMR), a structured parent-report survey measuring adherence to multiple lethal means restriction behaviors. Items are rated on a Likert scale, with total scores ranging from 11 to 55; higher scores indicate greater adherence.

Secondary outcomes

  1. Adolescent Perceived Access to Lethal Means

    Time frame: Baseline to 6 weeks

    Perceived Access to Lethal Means is a self-report measure assessing adolescents' perceptions of their access to potentially lethal methods. Items assess the perceived ease of access, with total scores ranging from 5 to 30; higher scores indicate greater perceived access to lethal means.

Other outcomes

  1. Exploratory Outcome

    Time frame: Baseline to 12 weeks

    Number of participants (adolescents) with a suicide-related Emergency Department revisit and/or suicide attempt within 12 weeks post-randomization

Study contacts

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

Amy Conger

CONTACT

[email protected]

214-4562705

Matthew Nguyen

CONTACT

[email protected]

469-509-2493

Sponsors and collaborators

Lead sponsor

University of Texas Southwestern Medical Center

Other

Collaborators

  • The Texas Child Mental Health Care Consortium (TCMHCC)

Registry information

Official study title

Nudging Parental Action With A Randomized Controlled Trial of Text Messaging Intervention for Suicide Prevention

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Feb 3, 2026
Registry last updated
Jun 3, 2026

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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