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临床试验/NCT05128227
NCT05128227已完成不适用

PHARM-S.A.V.E.S: Suicide Prevention Gatekeeper Training for Pharmacy Staff

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 119 人开始时间: 2022年4月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
119
试验地点
2
主要终点
Change in proportion of participants who ask about suicide.

研究概览

简要总结

This is a pilot Randomized Controlled Trial (RCT) in which 150 pharmacy staff members will be randomized to an experimental or control group and data on suicide prevention communication and secondary outcomes will be collected over the course of the RCT.

详细描述

This is a prospective pilot RCT that will evaluate the impact of suicide prevention gatekeeper training (Pharm-SAVES) on 150 pharmacy staff member communication behaviors (primary outcome). Data will be collected at baseline, immediately after training is completed, and at 1-month follow up. Data sources include simulated patient observations (to rate quality of communication) and survey data (for self-reports of knowledge, self-efficacy, and referral behaviors).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Staff must:
  • be at least 18 years of age;
  • read and speak English; and
  • be currently employed as a pharmacist or pharmacy technician at a community pharmacy

排除标准

  • Individuals will be excluded if they hold floater status (non-staff pharmacists or technicians).

结局指标

主要结局

Change in proportion of participants who ask about suicide.

时间窗: Baseline and immediately post-intervention

An online survey will include a written case that asks participants what they would say to a patient who has expressed verbal suicide warning sign(s). Blinded coders will review the open-ended response to determine whether the participant asks about suicide. The responses will be coded as no=0 and yes=1.

次要结局

  • Change in proportion of participants who report they would call the National Suicide Prevention Lifeline.(Baseline and immediately post-intervention)
  • Change in suicide prevention knowledge score from baseline to immediate post-intervention.(Baseline and immediately post-intervention)
  • Change in mean suicide prevention self-efficacy score from baseline to 1-month follow-up(Baseline and 1-month follow-up)
  • Change in mean suicide prevention preparedness score from baseline to 1-month follow-up.(Baseline and 1-month follow-up)
  • Proportion of participants who ask about suicide (optional)(1-month follow-up)
  • Change in mean suicide prevention self-efficacy score from baseline to immediate post-intervention.(Baseline and immediately post-intervention)
  • Change in mean suicide prevention preparedness score from baseline to immediate post-intervention.(Baseline and immediately post-intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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