Introduction Seminar About Patient Participation and Treatment Options for Psychiatric Patients on Waiting List
Introduction Seminar About Patient Participation and Treatment Options for Patients on Waiting List in a Community Mental Health Centre - Development, Effect, Experiences and Costs
Patient participation is a central concept in Norwegian health policy. It is mandatory in hospitals and emphasised as one of the most prioritised areas by the Government. Studies from Norway have repeatedly found that patients who seek help in community mental health centres ("DPS") are dissatisfied with the information they receive and about their possibility for real influence in their treatment.
One way to improve individual patient participation might be to give patients information before they start their treatment. This can be done as group based patient education to reduce the resources needed. Furthermore, as there are waiting lists for treatment, such introduction seminars could be held while patients are waiting to use this time in a meaningful way.
The present study therefore aims at testing the effect of an introduction seminar for patients on waiting list in a community mental health centre.
研究概览
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
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Trondheim、挪威、7055
- Tiller DPS
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Patients older than 18 years referred for out patient treatment who get a guarantee of starting treatment between 2 and 6 months will be included.
Exclusion Criteria:
- patients with a guarantee of starting treatment in less than two months and
- patients who do not understand the consequences of taking part in the study
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
---|---|
有源比较器:日常护理
|
日常护理
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实验性的:Introduction seminar
Psychoeducation for patients on waiting list
|
The seminar will be held over two half days, each lasting 2.5 hours.
Up to 30 patients can participate in each seminar.
The details of the content of the program will be developed based on study one.
The preliminarily plans are to give general information about the community mental health centre, the available treatment options and patients rights by presentations from health personnel and user representatives.
At the end of each day, the patients will be divided into small groups mentored by health personnel were they can discuss the presentations and ask questions.
In the breaks, literature and other type of information for patients will be on display.
All participants will get a folder with details of the program and leaflets from patient organisations and governmental agencies.
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Behavior and symptoms
大体时间:12 months
|
Behavior and Symptom Identification Scale (BASIS-32)
|
12 months
|
knowledge on treatment preference
大体时间:1 month
|
1 month
|
|
patient activation (coping)
大体时间:4 months
|
measured with Patient Activation Measure (PAM)
|
4 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
---|---|---|
Client satisfaction
大体时间:Baseline, 4 and 12 months
|
Satisfaction measured with Client Satisfaction Questionnaire (CSQ-8)
|
Baseline, 4 and 12 months
|
Perceived participation
大体时间:Baseline, 4 and 12 months
|
Perceived participation measured with Perception of care (PoC)
|
Baseline, 4 and 12 months
|
Psychiatric Out-Patient Experiences
大体时间:Baseline, 4 and 12 months
|
Psychiatric Out-Patient Experiences Questionnaire (POPEQ)
|
Baseline, 4 and 12 months
|
Quality of Life
大体时间:Baseline, 4 and 12 months
|
WHO-5
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Baseline, 4 and 12 months
|
motivation for treatment
大体时间:Baseline, 1 and 4 months
|
motivation for treatment (questions)
|
Baseline, 1 and 4 months
|
costs
大体时间:Baseline, 1, 4 and 12 months
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data on health care use, sick leave, medication and other direct and indirect costs will be collected
|
Baseline, 1, 4 and 12 months
|
Knowledge
大体时间:Baseline, 1, 4 and 12 months
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measured using a self developed questionnaire
|
Baseline, 1, 4 and 12 months
|
合作者和调查者
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- Introduction seminar
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
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