Improving Our Understanding of Suicidal Ideation in Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 160
- 试验地点
- 1
- 主要终点
- Suicidal Ideation Information
研究概览
简要总结
The goal of this project is to assess the feasibility of collecting physiological and psychological data that will allow for preliminary investigation of predictors of suicidal ideation in an ambulatory cancer population already seeking psychosocial support.
详细描述
Exploratory analyses will be the first step to establishing possible predictive relationships. The long-term goal of this research is to identifying an integrated model of suicidal ideation in cancer, so that providers will be better able to identify appropriate screening methods to target patients at high risk for suicide. This information will ultimately inform the development of psychosocial interventions that specifically address the variables that increase suicide risk in patients with cancer.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 100 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- •Provision to sign and date the consent form.
- •Stated willingness to comply with all study procedures and be available for the duration of the study.
- •Be male or female, aged 18 or older.
- •Ambulatory oncology patients at the University of Colorado Cancer Center who are being provided psychosocial support services; specifically, having had at least one in-person meeting with a doctoral level clinical/counseling psychologist or masters level social worker.
- •Valid and private email account.
排除标准
- 未提供
结局指标
主要结局
Suicidal Ideation Information
时间窗: duration of study, no more than 2 weeks
To evaluate the feasibility of data collection regarding physiological and psychological factors influencing suicidal ideation in cancer survivors
次要结局
- Pain Intensity(duration of study, no more than 2 weeks)
- Physical Functioning(duration of study, no more than 2 weeks)
- Suicidal Ideation(duration of study, no more than 2 weeks)
- Experiential Avoidance(duration of study, no more than 2 weeks)
- Depression(duration of study, no more than 2 weeks)
- Hopelessness(duration of study, no more than 2 weeks)
- Pain Interference(duration of study, no more than 2 weeks)
- Symptom Burden/Severity(duration of study, no more than 2 weeks)
- Health Related Quality of Life(duration of study, no more than 2 weeks)
- Anxiety(duration of study, no more than 2 weeks)
- Demoralization(duration of study, no more than 2 weeks)
- Desire for Hastened Death(duration of study, no more than 2 weeks)