NCT03604380已完成不适用
STATE Trial: SusTained Attention Training to Enhance Sleep (Phase I- Remote Trial Arm)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 134
- 试验地点
- 2
- 主要终点
- Sleep duration scores on the Pittsburg Sleep Quality Index
研究概览
简要总结
This study is a validation study to document the acceptability of the Tonic and Phasic Alertness Training (TAPAT) program in older adults with chronic late-life insomnia. The goal of this study is to employ a computerized attention-training program, TAPAT, designed for chronic late-life insomnia in a remote, randomized, controlled trial to assess feasibility and initial efficacy in this population.
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
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 55 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Participant must be 55 years of age or older.
- •Participant must meet criteria for clinical insomnia - moderate severity based on the Insomnia Severity Index.
- •Participant must be a fluent English speaker.
- •Participant must have adequate visual, auditory, and motor capacity to use computerized intervention.
- •Participant must have a computer and access to the Internet.
排除标准
- •Participants with untreated psychiatric conditions, including substance abuse/dependence disorders, untreated obstructive sleep apnea, diagnosis of other sleep disorders (e.g., restless legs syndrome), recent hospitalization, ongoing chemotherapy or other cancer treatment, and concurrent engagement in another insomnia treatment.
- •Participants enrolled in another concurrent research study.
- •Participants using computer-based cognitive training programs or has used them within a month of the consent date.
结局指标
主要结局
Sleep duration scores on the Pittsburg Sleep Quality Index
时间窗: 6 months
Sleep efficiency scores on the Pittsburg Sleep Quality Index
时间窗: 6 months
次要结局
未报告次要终点
研究者
研究点 (2)
Loading locations...
相似试验
已完成
不适用
STATE Trial: SusTained Attention Training to Enhance SleepInsomniaNCT02921074Posit Science Corporation23
已完成
不适用
Double-Blind Randomized Controlled Trial for the Evaluation of a Novel Adaptive Attention Training in Healthy AdolescentsHealthy AdolescentsNCT03213613University of California, San Francisco60
已完成
不适用
Attention Control Training for PTSD in ChildrenPTSDNCT03348540Creighton University89
已完成
不适用
Attention Control Training for PTSD Related to Combat or Interpersonal ViolencePTSDNCT03350360Creighton University73
已完成
不适用
Evaluation of a School-Based Attention Training Programme for Improving ConcentrationAttention Concentration DifficultyNCT04698577University of Limerick36
