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N/A N=4 Treatment

A Feasibility Open Trial of App-Enhanced Brief CBT for Suicidal Inpatients

Suicidal and Self-injurious Behavior

Enrolled (actual)
4
Serious AEs
0.0%
Results posted
Aug 2024
Primary outcome: Primary: Client Satisfaction at Discharge — 29.00 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
App-Enhanced Brief Cognitive-Behavioral Therapy (Behavioral)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Hartford Hospital
Primary completion
Feb 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Client Satisfaction at Discharge
29.00
PRIMARY
App Usability at Discharge
95.00
PRIMARY
Frequency of Suicide Attempts
PRIMARY
Suicidal Ideation Baseline
82.00
PRIMARY
Suicidal Ideation at Discharge
46.67
PRIMARY
Suicidal Ideation 1 Month
21.00
PRIMARY
Suicidal Ideation 2 Months
25.00
PRIMARY
Suicidal Ideation 3 Months
45.00

Summary

The purpose of this study is to evaluate the feasibility of integrating Brief Cognitive-Behavioral Therapy (BCBT) counseling with a software application (app) to prevent future suicidal thoughts and behaviors.

Eligibility Criteria

Inclusion Criteria

  • History of suicide attempt (lifetime) AND active ideation (with or without plan or intent) on admission
  • Own and have access to their phone (iPhone or Android with capability to download apps) during their inpatient stay
  • Ability to understand the nature of the study and provide written informed consent
  • Willing and able to provide at least two verifiable contacts for emergency or tracking purposes
  • Expected length of stay long enough to complete the entire treatment protocol

Exclusion Criteria

  • Not fluent in English
  • Experiencing current mania or psychosis
  • Have lifetime history of schizophrenia spectrum disorder, intellectual disability, or organic brain illness
  • Inpatient treatment plan includes detox protocol or electroconvulsive therapy
  • Any other psychiatric or medical condition that in the investigator's opinion would preclude informed consent or participation in the trial
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05486091). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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