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临床试验/NCT06170255
NCT06170255已完成1 期

Depression Treatment and Risk for Cardiovascular Disease

East Carolina University0 个研究点目标入组 16 人开始时间: 2014年3月6日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
已完成
入组人数
16
主要终点
Feasibility

研究概览

简要总结

This study was designed to determine the feasibility of a Randomized Controlled Trial (RCT) that involved treating depression among participants with an elevated risk for cardiovascular disease. It is expected that treating depression through non-pharmacological means will impact heart rate variability, a proximal measure of CVD risk.

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
21 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Males and females age 21-75
  • •Meet diagnostic criteria for major depressive disorder
  • •Framingham risk score indicating a greater than negligible 10-year risk (3% or greater) for cardiovascular disease.
  • •Levels of depressive symptoms of at least moderate level (beck depression inventory II score > 19 of 63 possible points; or a Hamilton depression rating scale > 12 of 50 possible points)

排除标准

  • •A verbal expression of current, significant, suicidal ideation; a score of > 15 on the beck scale for suicidal ideation
  • •Score of >1 on any single item of the Beck Scale for Suicidal Ideation
  • •Score of > 1 on the item assessing suicidal ideation on the beck depression inventory II.
  • •Psychiatric diagnoses that could potentially interfere with depression treatment (current post traumatic stress disorder, bipolar I disorder, obsessive-compulsive disorder, bulimia or anorexia nervosa, schizophrenia, and panic disorder)
  • •Current use of an antidepressant medication
  • •Currently in psychotherapy.
  • •Current use of a beta blocker, anxiolytic (benzodiazepine), antipsychotic agent
  • •Diagnosis of CVD.

研究组 & 干预措施

Depression treatment

Experimental

Participants receive behavioral therapy for depression

干预措施: Behavioral Activation (BA) (Behavioral)

结局指标

主要结局

Feasibility

时间窗: 2 years. Throughout the course of the study (number recruited/screened, number enrolled, number completing the study)

Feasibility of the study including recruitment, enrollment, and retention rates

次要结局

  • Heart Rate Variability (HRV)(12 weeks)

研究者

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

Matthew Whited

Associate Professor of Psychology

East Carolina University

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