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临床试验/NCT02382562
NCT02382562终止不适用

Brief Behavioral Activation Intervention for Depressed Asthma and Urticaria Patients

University of Mississippi Medical Center2 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2015年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
18
试验地点
2
主要终点
Urticaria Control Test

研究概览

简要总结

Depression and other unhealthy behaviors, such as not taking medication as prescribed and not attending doctor visits have been suggested to increase the worsening of allergic diseases (e.g. asthma, urticaria). We intend to determine whether a one-session behavioral intervention is effective in helping with depression and controlling disease symptoms. We will measure this using pre- and post-intervention surveys.

详细描述

The purpose of this research study is to investigate whether a one-session behavioral activation intervention for depression can successfully reduce depression and improve asthma or urticaria disease-relevant outcomes (medication adherence, doctor's visits, substance abuse) in clinical patients with asthma or urticaria who report heightened levels of depression and are seen in the UMMC Allergy Clinic.

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 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Potential participants should be between the ages 18 and 64, seen in the UMMC Allergy Clinic with either asthma or urticaria and who report symptoms of depression in the previous 2 weeks.

排除标准

  • Potential participants younger than 18 and older than 64 or who do not speak English or cannot comprehend the consent form or women who are pregnant are excluded.

研究组 & 干预措施

Brief Behavioral Activation Intervention

Experimental

All eligible participants will undergo the Brief Behavioral Activation Intervention.

干预措施: Brief Behavioral Activation Intervention (Behavioral)

结局指标

主要结局

Urticaria Control Test

时间窗: 4 weeks

Changes in urticaria control over a 4 week period.

Asthma Control Test

时间窗: 4 weeks

Changes in asthma control over a 4 week period.

次要结局

  • Asthma Quality of Life Questionnaire(4 weeks)
  • Psychological Measures (Composite)(4 weeks)
  • Urticaria Activity Score Questionnaire(4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gailen D. Marshall Jr., MD PhD

Gailen D. Marshall, Jr., MD, PhD

University of Mississippi Medical Center

研究点 (2)

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