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The Effects of Peer Co-led Educational Group Intervention for Adults With Attention-Deficit Hyperactivity Disorder (ADHD)

The Effects of Peer Co-led Educational Group Intervention for Adults With Attention-Deficit Hyperactivity/Impulsivity Disorder

Peer co-led education describes educators who are expert patients, user representatives or former patients, participating and teaching in educational interventions in cooperation with health care professionals. Peer co-led education is included in the Norwegian national guidelines for treatment of mental disorders, but despite some promising results for the treatment of other conditions, still little is known about the efficacy of peer co-led educational group interventions interventions for adults with attention deficit and hyperactivity disorder (ADHD).

This pilot trial will evaluate patient satisfaction with and preliminary efficacy of a 2-session peer co-led educational group program designed to address specific challenges faced by adults diagnosed with ADHD at an outpatient clinics in mid-Norway.

研究概览

研究类型

介入性

注册 (实际的)

56

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Trondheim、挪威、7055
        • Tiller DPS

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 67年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Confirmed ADHD-diagnosis
  • speaking a Scandinavian language

Exclusion Criteria:

  • Unable to give informed consent
  • Psychosis
  • Severe learning difficulties

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Educational intervention
Patients randomized to the intervention group will start with a group-based educational program immediately after the randomization.
The group-based educational program consists of two sessions that run over two consecutive weeks. Each session consists of a lecture from a recruited expert on the topic of the session and by expert patients with a following discussion of the topic facilitated by the course leader.
其他名称:
  • 患者教育
Diagnostic treatment with medication. In addition, some patients receive cognitive behavioral therapy (not systematically given to every patient). If needed, patients are also offered assistance with regard to economy, housing, education, and work as well as contact with family and network.
其他名称:
  • 照常治疗
有源比较器:Waiting list
Participants randomized to the waiting list control group receive no educational intervention for the duration of the 10 weeks. During this period participants can receive standard treatment, consisting of diagnostic treatment with medication.
Diagnostic treatment with medication. In addition, some patients receive cognitive behavioral therapy (not systematically given to every patient). If needed, patients are also offered assistance with regard to economy, housing, education, and work as well as contact with family and network.
其他名称:
  • 照常治疗
No educational intervention for the duration of the 10 weeks. During this period participants can receive standard treatment.

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
Change in client Satisfaction
大体时间:from baseline to 2-weeks follow-up
Client satisfaction will be measured with Client Satisfaction Questionnaire, short form (Attkisson & Zwick, 1982). The scale consists of 8 items scored on a Likert scale from 1 (low satisfaction) to 4 (high satisfaction). Total scores range from 8 to 32, with higher scores indicating greater satisfaction.
from baseline to 2-weeks follow-up
change in patient activation
大体时间:from baseline to 10-weeks follow-up
Patient activation will be measured with the Norwegian version of the Patient Activation Measure Mental Health (PAM-MH) (Green et al 2010))
from baseline to 10-weeks follow-up

次要结果测量

结果测量
措施说明
大体时间
change in general self-efficacy
大体时间:from baseline to 10 weeks follow-up
General Self-Efficacy Scale, 6-item scale ranging from 1 ('not at all true') to 4 ('exactly true'). Total scores range from 6 to 24, with higher scores indicating greater self-efficacy. (Romppel et al 2013)
from baseline to 10 weeks follow-up
change in ADHD-related symptoms
大体时间:from baseline to 10 weeks follow-up
Hopkin's Symptom Checklist (SCL), 9-items scale with high scores on SCL-9 indicating ADHD-related symptom burden (Eich et al 2011)
from baseline to 10 weeks follow-up
change in ADHD-related symptoms
大体时间:from baseline to 10 weeks follow-up
Norwegian version of the WHO Adult ADHD Self-report scale, ASRS Short Form (Kessler et al 2005)
from baseline to 10 weeks follow-up
change in Quality of Life
大体时间:from baseline to 10 weeks follow-up
Adult Attention Deficit/Hyperactivity Disorder Quality of Life Scale, AAQoL short Form (Brod et al 2006)
from baseline to 10 weeks follow-up

其他结果措施

结果测量
措施说明
大体时间
Use of health services and work participation
大体时间:through study completion, an average of 24 weeks
Self-reported work participation and received services: 3 questions about both work status and received treatment
through study completion, an average of 24 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

合作者

调查人员

  • 研究主任:Anne-Lise Løvaas, md phd、St. Olavs Hospital

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2018年5月31日

初级完成 (实际的)

2020年3月15日

研究完成 (实际的)

2020年3月15日

研究注册日期

首次提交

2018年4月25日

首先提交符合 QC 标准的

2018年6月5日

首次发布 (实际的)

2018年6月6日

研究记录更新

最后更新发布 (实际的)

2022年1月27日

上次提交的符合 QC 标准的更新

2022年1月25日

最后验证

2021年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

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.

Group-based education的临床试验

3
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