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临床试验/NCT00149773
NCT00149773已完成1 期

Cognitive Therapy for Suicidal Older Men in Primary Care Settings

University of Pennsylvania2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2005年5月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
34
试验地点
2
主要终点
Suicidal Ideation; measured at Months 1, 3, 6, 12, 18, and 24

研究概览

简要总结

This study will assess the effectiveness of cognitive therapy in reducing the incidence of suicide ideation and behavior in older men in a primary care setting.

详细描述

Older adult males have the highest suicide rate of any age group in the U.S. Over 70 percent of older suicide victims have been to their primary care physician within a month of their death, many with a depressive illness that was not detected. However, most research concerning treatments for suicide ideation and behavior has focused on adolescents and young adults. Very few treatments have been developed to reduce suicide ideation and behavior in men aged 60 and above. This study will assess the effectiveness of specialized cognitive therapy versus typical treatment in treating older men with suicide ideation.

Participants in this two-year, single-blind study will be randomly assigned to receive either cognitive therapy combined with enriched care or enriched care alone. Participants will be identified in primary care settings as having experienced suicide ideation in the past month. Cognitive therapy will be provided by Ph.D.-level therapists and will be geared specifically toward older men with suicidal tendencies. The enriched care condition will consist of the usual care that individuals receive for suicide prevention, plus assessment and referral services provided by independent evaluators and study case managers. All participants will be assessed pre-treatment to attain baseline measures of suicide ideation, hopelessness, and depression. Study visits will occur at baseline and Months 1, 3, 6, 12, 18, and 24 to assess suicide ideation. Self-report and clinician-administered measures will be used to assess participants' progress.

For information on a related study, please follow this link:

http://clinicaltrials.gov/show/NCT00218725

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
60 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Currently experiencing death ideation or suicidal ideation (total score greater than 0 on the Scale for Suicide Ideation)
  • English-speaking
  • Lives within the area served by the research unit
  • Able to provide at least 2 verifiable contacts (typically family members)

排除标准

  • Requires priority treatment for an acute, unstable, or severe Axis III disorder (e.g., dementia)
  • Requires priority treatment for another debilitating problem (e.g., severe alcohol or drug dependence, mania, severe anorexia)
  • Suffers from a psychotic disorder or psychotic thought processes
  • Exhibits self-mutilating behavior without any intent to commit suicide (e.g., burning oneself with a cigarette)

结局指标

主要结局

Suicidal Ideation; measured at Months 1, 3, 6, 12, 18, and 24

时间窗: 1, 3, 6, 12, 18, and 24 months

次要结局

  • Depression; measured at Months 1, 3, 6, 12, 18, and 24(1, 3, 6, 12, 18, and 24 months)
  • Perceived Social Support; measured at Months 1, 3, 6, 12, 18, and 24(1, 3, 6, 12, 18, and 24 months)
  • Hopelessness; measured at Months 1, 3, 6, 12, 18, and 24(1, 3, 6, 12, 18, and 24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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