跳至主要内容
临床试验/NCT03665298
NCT03665298撤回不适用

Needle-X: Usability Testing of a Smartphone Application

NYU Langone Health1 个研究点 分布在 1 个国家开始时间: 2019年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Feasibility of Needle-X application

研究概览

简要总结

Mobile health interventions offer a longitudinal approach to reducing the burden of substance use disorders and may stem the rise of the opioid overdose epidemic. Smartphone applications are one of the most popular mobile phone features nationally, among patients in addiction treatment, and among criminal justice involved (CJI) patients enrolled in addiction treatment. This research conducted at Bellevue Hospital's inpatient detoxification program established attitudes and self-reported behaviors favorable to theoretical smartphone applications addressing opioid use, HIV, and HCV prevention and management strategies. This study aims to assess the feasibility and usability of a smartphone application to enhance access to sterile needles, naloxone overdose kits, and addiction treatment programs in New York City.

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
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Fluent in spoken and written English;
  • •Meets or has previously met DSM-5 criteria for current opioid use disorder, of at least moderate severity;
  • •Owns or has owned a smartphone

排除标准

  • •Any patient who does not meet the inclusion criteria as above, is clinically unstable per the unit admitting physicians, refuses to participate in the study, or is cognitively impaired.

研究组 & 干预措施

Needle X

Experimental

Smartphone application application to enhance access to sterile needles, naloxone overdose kits, and addiction treatment programs in New York City.

干预措施: Smartphone Application (Behavioral)

结局指标

主要结局

Feasibility of Needle-X application

时间窗: 12 Months

number of patients enrolled, as this study will include a single interaction, at which point the patient will no longer be part of the study.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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