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临床试验/NCT06013982
NCT06013982已完成不适用

Impact of a Structured Anxiety Reduction Program on Anxiety in Patients Who Are Discharged to Home Following an Acute Stroke in an Academic Medical Center

NYU Langone Health1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2023年8月22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
34
试验地点
1
主要终点
Change in GAD-7 Score from Baseline to Month 3

研究概览

简要总结

The purpose of this pilot study is to explore the impact that a structured anxiety reduction intervention program has on patients being discharged to home following an acute stroke in an academic medical center. Eligible participants will be screened and recruited by the research team through daily rounds. After completing the informed consent process, the research team will pull demographic information from the electronic health record (EHR) and REDCAP that includes ethnicity and support system. Participants will complete the Anxiety Screen Questionnaire (GAD-7 ANXIETY SURVEY) and will be provided with information regarding stroke support groups available with additional NYU Langone Health and the American Heart Association internet-based information regarding anxiety reduction (NYU Langone Health Anxiety Reduction Bundle). The participants will be encouraged to attend a stroke support group for 3 months and utilize the NYU Langone Health Anxiety Reduction Bundle provided. At the completion of the intervention (3 months), participants will be provided with the GAD-7 ANXIETY SURVEY again and a survey that includes open-ended questions and a program evaluation by email. Analysis will occur after final data is collected.

研究设计

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

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Be diagnosed with an acute stroke
  • •Able to speak, read and write in English
  • •Not cognitively impaired, as per standard of care documentation in the EHR regarding mental status.
  • •Discharged to home
  • •Internet access including email
  • •Willingness to participate in an anxiety reduction program
  • •Length of hospital stay less than 5 days from the initial presentation of stroke symptoms
  • •Must be medically stable

排除标准

  • •Not diagnosed with an acute stroke
  • •Unable to speak, read and write in English as this intervention is not available in other languages and at this time, funding is not available in order to have the resources provided translated or to have translation services available for these participants.
  • •Not discharged to home
  • •No internet access including email
  • •Unwilling or unable to participate in an anxiety reduction program
  • •Cognitively impaired
  • •Length of hospital stay greater than 6 days from the initial presentation of stroke symptoms
  • •Not medically stable

研究组 & 干预措施

Patients discharged following acute care stroke

Experimental

Participation will last 3 months from enrollment. Demographic data will be retrieved from the electronic health record and the Generalized Anxiety Disorder-7 (GAD-7) Anxiety Questionnaire will be administered at baseline. Participants will repeat the GAD-7 in 3 months and an additional qualitative survey on their experience including an evaluation of the structured anxiety reduction program.

干预措施: Anxiety Reduction Bundle (Behavioral)

结局指标

主要结局

Change in GAD-7 Score from Baseline to Month 3

时间窗: Baseline, Month 3

The GAD-7 Anxiety Questionnaire involves 7 items assessing how often participants have felt bothered by anxiety-related problems over the past two weeks. Each item is rated on a Likert scale from 0 (not at all) to 3 (nearly every day). The total score is the sum of responses and ranges from 0-21; where 0-4 = minimal anxiety; 5-9 = mild anxiety; 10-14 = moderate anxiety; 15-21 = severe anxiety.

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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