Exploring the Transferability of Improving Access to Psychological Therapies (IAPT) to a General Hospital Emergency Inpatient Ward
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Number of participants with moderate or severe anxiety
研究概览
简要总结
Prevalence of anxiety and depression in the general population is known, but is under researched in the acute hospital setting and there is little evidence on the prevalence of anxiety and depression within the emergency medical admission population. A potential intervention for treating such mental health prevalence would be in the form of IAPT methodology which has been utilised in other parts of the NHS demonstrating good outcomes. Therefore, this feasibility study will explore the utility of IAPT in the acute setting.
This study will explore the prevalence of anxiety and depression in the emergency medical population within medical inpatient wards , utilising the assessment tools adopted by the IAPT services and explained in detail below.
The study will explore a) feasibility of introducing psychological intervention to an emergency medical ward and b) provide preliminary data on the outcome of this intervention on hospital length of stay and readmission rates.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Patients admitted to Ipswich Hospital into a ward that cares for patients who are medical emergencies.
- •Patients who score 3 or higher on one or both of the GAD 2 and PHQ
- •Patients that have capacity to consent.
- •Over 18 years old.
- •Ability to speak and read in English as the study will not have the resources to employ interpreters or to get documentation translated.
- •Participants that are not deemed suicidal via screening and medical and nurse assessment.
排除标准
- •Patients not receiving care on a ward caring for medical emergencies.
- •Patients under the age of 18 years old.
- •Patients scoring < 3 on both GAD 2 and PHQ
- •Patients who do not have capacity to consent.
- •Participants that are suicidal as via screening and medical and nurse assessment.
研究组 & 干预措施
IAPT
干预措施: Improving access to psychological therapies (IAPT) (Other)
结局指标
主要结局
Number of participants with moderate or severe anxiety
时间窗: Up to 6 months
How many participants enrol in to the study, that are eligible to participate.
次要结局
- IAPT views(Up to 6 months)