Actively Recruiting

Phase Not Applicable
Age: 11Years - 18Years
All Genders
NCT05390918

Targeting Adolescent Insomnia to Lessen Overall Risk of Suicidal Behavior

Led by Jeff Bridge · Updated on 2026-02-05

235

Participants Needed

1

Research Sites

223 weeks

Total Duration

On this page

Sponsors

J

Jeff Bridge

Lead Sponsor

C

Centers for Disease Control and Prevention

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will test the effectiveness of a sleep-related primary suicide prevention program entitled TAILOR (Targeting Adolescent Insomnia to Lessen Overall Risk of Suicidal Behavior), which includes specific behavior-change strategies for adolescents at risk of suicidal behavior who suffer from difficulties falling asleep, staying asleep, and/or insufficient sleep.

CONDITIONS

Official Title

Targeting Adolescent Insomnia to Lessen Overall Risk of Suicidal Behavior

Who Can Participate

Age: 11Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Must be a patient of Nationwide Children's Hospital
  • Aged between 11 years, 0 months and 18 years, 11 months at time of consent
  • Have recent suicidal ideation within the past 90 days
  • Have sleep problems within the past 30 days
  • Live with a primary caregiver who can legally consent to research participation
Not Eligible

You will not qualify if you...

  • Suicide attempt within the past 3 months
  • Diagnosis of Bipolar Disorder or Psychosis
  • Change to antipsychotic or mood stabilizer medication in last 2 months
  • Snoring at least 3 nights per week audible from a room or two away
  • Gasping for air while sleeping, diagnosis of Obstructive Sleep Apnea, or turning blue within past year
  • Body Mass Index over 40
  • Daytime symptoms of Restless Leg Syndrome
  • Diagnosis of Narcolepsy
  • Diagnosis of Seizures or Epilepsy or prescribed anticonvulsants within last 4 years
  • Significant substance use in past month
  • Currently receiving sleep disorder services from a sleep clinic
  • Inability to speak or read English well enough to understand study consent and procedures
  • No access to a telephone or internet device
  • Sibling already enrolled in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Nationwide Children's Hospital

Columbus, Ohio, United States, 43205

Actively Recruiting

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Research Team

E

Elizabeth Cannon, MA, MS

CONTACT

K

Kendra Heck, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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