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临床试验/NCT04896593
NCT04896593已完成不适用

Mobile Technology for Reducing and Preventing Adolescent Suicide

Hartford Hospital1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2021年7月12日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
22
试验地点
1
主要终点
App Usability 16 Weeks

研究概览

简要总结

This single-group open-label trial will evaluate the feasibility and preliminary efficacy of a suicide prevention mobile application when used as an adjunct to usual care in adolescents.

详细描述

This study will enroll 20 adolescent (age 13-17) inpatients at elevated risk for suicide. Participants will download the app onto their phones during their inpatient stay and will complete a single therapy session involving psychoeducation and crisis response planning. Participants will be encouraged to use the app on their own in addition to their usual outpatient services to learn and practice suicide prevention skills. Participants and their parents will be interviewed 1, 4, 8, 12, and 16 weeks after discharge.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
13 Years 至 17 Years(Child)
性别
All
接受健康志愿者
否

入选标准

  • •Inpatient psychiatric patients who have attempted suicide (lifetime) or have documented suicide ideation and a plan to harm themselves at admission
  • •Understand written and spoken English
  • •Own an iPhone with iOS 11 or higher, or Android with OS 8.1 or higher
  • •Willing and able to complete enrollment procedures
  • •Parent/guardian (and youth) able to understand the nature of the study and provide written informed consent (assent for youth)
  • •Willing to agree to release of information to their parent/guardian and providers when clinically indicated.
  • •Discharge plan includes aftercare within the Hartford HealthCare system (to facilitate coordination of care during follow up)

排除标准

  • •Patients with active psychosis
  • •Patients experiencing substance withdrawal
  • •Currently enrolled in other treatment studies for the symptoms and behaviors targeted
  • •Patient unwilling or unable to wear mask during in-person study procedures
  • •Patients who, in the judgment of the investigator, would have an unfavorable risk/benefit profile with respect to the Smartphone App.
  • •Any other psychiatric or medical condition (e.g., intellectual disability) or custody arrangement that in the investigator's opinion would preclude informed consent/assent or participation in the trial.

研究组 & 干预措施

Intervention

Experimental

Smartphone app teaching suicide prevention skills.

干预措施: Smartphone App (Behavioral)

结局指标

主要结局

App Usability 16 Weeks

时间窗: 16 weeks post discharge

The System Usability Scale (SUS) contains 10 items assessing the usability of digital technology. Items are rated from 1 to 5 with higher numbers representing stronger agreement with usability statements. Scores can range from 0 to 100, with higher scores reflecting better outcomes, meaning increased usability of the technology. The mean and standard deviation for the SUS will be reported utilizing all available data.

App Usability 1 Week

时间窗: 1 week post discharge

The System Usability Scale (SUS) contains 10 items assessing the usability of digital technology. Items are rated from 1 to 5 with higher numbers representing stronger agreement with usability statements. Scores can range from 0 to 100, with higher scores reflecting better outcomes, meaning increased usability of the technology. The mean and standard deviation for the SUS will be reported utilizing all available data.

App Usability 4 Weeks

时间窗: 4 weeks post discharge

The System Usability Scale (SUS) contains 10 items assessing the usability of digital technology. Items are rated from 1 to 5 with higher numbers representing stronger agreement with usability statements. Scores can range from 0 to 100, with higher scores reflecting better outcomes, meaning increased usability of the technology. The mean and standard deviation for the SUS will be reported utilizing all available data.

App Usability 8 Weeks

时间窗: 8 weeks post discharge

The System Usability Scale (SUS) contains 10 items assessing the usability of digital technology. Items are rated from 1 to 5 with higher numbers representing stronger agreement with usability statements. Scores can range from 0 to 100, with higher scores reflecting better outcomes, meaning increased usability of the technology. The mean and standard deviation for the SUS will be reported utilizing all available data.

App Usability 12 Weeks

时间窗: 12 weeks post discharge

The System Usability Scale (SUS) contains 10 items assessing the usability of digital technology. Items are rated from 1 to 5 with higher numbers representing stronger agreement with usability statements. Scores can range from 0 to 100, with higher scores reflecting better outcomes, meaning increased usability of the technology. The mean and standard deviation for the SUS will be reported utilizing all available data.

次要结局

  • Suicidal Ideation 1 Week(1 Week post discharge)
  • Suicidal Ideation Baseline(Baseline)
  • Suicidal Ideation 12 Weeks(12 Weeks post discharge)
  • Suicidal Ideation 4 Weeks(4 Weeks post discharge)
  • Suicidal Ideation 8 Weeks(8 Weeks post discharge)
  • Suicidal Ideation 16 Weeks(16 Weeks post discharge)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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