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临床试验/ISRCTN31789096
ISRCTN31789096已完成不适用

Randomised controlled feasibility trial of a web-based intervention to reduce consumption in people with 'hazardous and harmful' alcohol intake compared with a face-to-face intervention

niversity College London (UCL)/Royal Free London NHS Foundation Trust (UK)0 个研究点目标入组 200 人开始时间: 2014年4月16日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200

研究概览

简要总结

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Participants will be hazardous and harmful drinkers in north London, identified using a validated screening tool such as AUDIT, referred from primary care, secondary care, or self-referred, to CAS.
  • 2. Patients aged 18 or over at time of screening
  • 3. Diagnosis of an alcohol use disorder using AUDIT criteria (score 8 or over)
  • 4. Residing in a stable place of residence
  • 5. Providing informed consent for randomisation, treatment and follow-up
  • 6. Patients without prior internet experience, or without home access to the internet will be included, but will be offered additional training as part of their facilitated access to DYD.
  • All participants will be given information about local free or low-cost public internet access points, such as libraries, health centres and cluster rooms.

排除标准

  • 1. Patients undergoing treatment for substance use or primary drug dependence (excluding nicotine) in the past 90 days
  • 2. Already receiving help for an alcohol use disorder
  • 3. Outstanding legal issues likely to lead to imprisonment
  • 4. Severe mental or physical illness likely to preclude active participation in treatment or follow-up
  • 5. Severe physical dependency on alcohol (LDQ > 20)
  • 6. Unable to consult in English without an interpreter
  • 7. Pregnancy
  • 8. Patients with severe physical dependency or severe and complex co-existing physical or mental health problems will be referred for Tier 4 services in line with DH guidelines
  • 9. Patients at risk of high risk of self-harm or suicide will not be excluded, but will be referred back to their GP for additional help

研究者

发起方
niversity College London (UCL)/Royal Free London NHS Foundation Trust (UK)

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