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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-90
SponsorWeill Medical College of Cornell University

About this trial

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).

Eligibility criteria

Qualifiers

50-90 years old

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

Recent hospitalization for suicidal ideation or suicide attempt; at hospital admission, Columbia Suicide Severity Rating Scale (CSSR-S) ≥ 2, "Non-specific Active Suicidal Thoughts."

We will also include patients on psychotropics and on after-care community psychotherapy.

Disqualifiers

Current diagnosis of Psychotic Disorders; Diagnosis of Dementia

Cognitive Impairment (MMSE ≤ 24)

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

Aphasia, sensory problems, and/or inability to speak English.

Trial design

Treatments tested in this trial

  • WellPATH-PREVENT
  • Optimized WellPATH-PREVENT

Treatment groups

115 Participants
are divided into 3 treatment groups

Sponsors and collaborators

Weill Medical College of Cornell University

Lead sponsor

National Institute of Mental Health (NIMH)

Collaborator