ACTIVE_NOT_RECRUITING

Comparing Suicide Prevention Interventions to Guide Follow-up Care: The SPRING Trial

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Conditions

SuicideSuicide PreventionSuicide and Self-harmCaring Contactsbrief contact interventionadultadolescentprimary carebehavioral healthfollow-up care

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Pragmatic randomized controlled trial to compare the effectiveness of two-way Caring Contacts text messages vs. one-way Caring Contacts text messages vs. enhanced usual care for suicide prevention in adults and adolescents.

Official Title

Comparing the Effectiveness of Two-Way Caring Contacts Texts vs One-Way Caring Contacts Texts vs Enhanced Usual Care to Reduce Suicidal Behavior in Youth and Adults Screening At-Risk for Suicide in Primary Care or Behavioral Health Clinics

Quick Facts

Study Start:2023-12-29
Study Completion:2026-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06128239

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:12 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adolescents (12-17 years old) and adults (18+)
  2. * Response of "yes" to at least one item on the Columbia Suicide Severity Rating Scale (C-SSRS) six-item screener at a St. Luke's Health System (SLHS) primary care or behavioral health clinic, or electronic health record or provider note from an eligible encounter indicates suicide risk
  3. * Ability to send and receive text messages
  4. * Ability to receive phone calls
  5. * Ability to receive emails
  6. * Participant and legal guardian (if applicable) speak, read, and understand English
  7. * Accommodations may be made for individuals with impaired hearing
  1. * Individuals who participated in a previous randomized controlled trial in the same health system related to Caring Contacts (SPARC Trial or MHAPPS Trial)
  2. * Patients who are unable or unwilling to provide informed consent\*, for example, due to acute or chronic cognitive impairment (i.e.: acute psychosis, intoxication, or intellectual disability).
  3. * Primary Care Provider, Behavioral Health Provider, or Principal Investigator determines that participation in the research is not in the best interest of the patient or the study team.

Contacts and Locations

Principal Investigator

Anna K Radin, DrPH, MPH
PRINCIPAL_INVESTIGATOR
St. Luke's Health System

Study Locations (Sites)

St. Luke's Health System
Boise, Idaho, 83712
United States

Collaborators and Investigators

Sponsor: St. Luke's Health System, Boise, Idaho

  • Anna K Radin, DrPH, MPH, PRINCIPAL_INVESTIGATOR, St. Luke's Health System

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-12-29
Study Completion Date2026-03-31

Study Record Updates

Study Start Date2023-12-29
Study Completion Date2026-03-31

Terms related to this study

Keywords Provided by Researchers

  • Caring Contacts
  • brief contact intervention
  • adult
  • adolescent
  • primary care
  • behavioral health
  • follow-up care

Additional Relevant MeSH Terms

  • Suicide
  • Suicide Prevention
  • Suicide and Self-harm