RECRUITING

WellPATH-PREVENT: A Mobile Intervention for Middle-Aged and Older Adults Hospitalized for Suicidal Ideation or Attempt

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

The goal of this project is to test whether WellPATH-PREVENT (a novel, mobile psychosocial intervention) improves a specific aspect of emotion regulation, i.e., cognitive reappraisal ability, and reduces suicide risk in middle-aged and older adults (50-90 years old) who have been discharged after a suicide-related hospitalization (i.e. for suicidal ideation or suicide attempt).

Official Title

WellPATH-PREVENT: A Mobile Intervention for Middle-Aged and Older Adults Hospitalized for Suicidal Ideation or Attempt

Quick Facts

Study Start:2022-04-22
Study Completion:2026-09-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05183230

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:50 Years to 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 50-90 years old
  2. * Diagnosis (based on a modified SCID-5 Clinical Trials Version to assess DSM-5 diagnoses): Any DSM-5 except: current diagnosis of Psychotic Disorder; diagnosis of Dementia
  3. * Recent hospitalization for suicidal ideation or suicide attempt; at hospital admission, Columbia Suicide Severity Rating Scale (CSSR-S) ≥ 2, "Non-specific Active Suicidal Thoughts."
  4. * We will also include patients on psychotropics and on after-care community psychotherapy.
  1. * Current diagnosis of Psychotic Disorders; Diagnosis of Dementia
  2. * Cognitive Impairment (MMSE ≤ 24)
  3. * Acute or severe medical illness (i.e., delirium; decompensated cardiac, liver or kidney failure; major surgery; stroke or myocardial infarction during the three months prior to entry
  4. * Aphasia, sensory problems, and/or inability to speak English.

Contacts and Locations

Study Contact

Dimitris Kiosses, PhD
CONTACT
914-997-4381
dkiosses@med.cornell.edu
Laurie Evans, MS
CONTACT
914-682-9100
lad9011@med.cornell.edu

Principal Investigator

Dimitris Kiosses, PhD
PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University

Study Locations (Sites)

New York Presbyterian Hospital/Weill Cornell Medicine
New York, New York, 10065
United States
Weill Cornell Institute of Geriatric Psychiatry, Weill Cornell Medicine
White Plains, New York, 10605
United States

Collaborators and Investigators

Sponsor: Weill Medical College of Cornell University

  • Dimitris Kiosses, PhD, PRINCIPAL_INVESTIGATOR, Weill Medical College of Cornell University

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 Date2022-04-22
Study Completion Date2026-09-30

Study Record Updates

Study Start Date2022-04-22
Study Completion Date2026-09-30

Terms related to this study

Keywords Provided by Researchers

  • Older Adults
  • Middle Aged Adults

Additional Relevant MeSH Terms

  • Suicide, Attempted
  • Suicidal Ideation
  • Depression