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临床试验/DRKS00003277
DRKS00003277
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Increasing the efficiency of depression-screening using patient-targeted feedback: Randomized controlled trial - DEPSCREEN-INFO

Bundesministerium für Bildung und Forschung Dienstsitz Berlin0 个研究点目标入组 4,151 人2012年7月3日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
F32
发起方
Bundesministerium für Bildung und Forschung Dienstsitz Berlin
入组人数
4151
状态
已完成
最后更新
去年

概览

简要总结

Background: International guidelines advocate depression screening in patients with coronary heart disease (CHD) and other chronic illnesses, but evidence is lacking. Aims: To test the differential efficacy of written patient-targeted feedback v. no written patient feedback after depression screening. Method: Patients with CHD or hypertension from three cardiology settings were randomised and screened for depression (ClinicalTrials.gov Identifier: NCT01879111). Compared with the control group, where only cardiologists received written feedback, in the intervention group both cardiologists and patients received written feedback regarding depression status. Depression severity was measured 1 month (primary outcome) and 6 months after screening. Results: The control group (n = 220) and the patient-feedback group (n = 155) did not differ in depression severity 1 month after screening. Six months after screening, the patient-feedback group showed significantly greater improvements in depression severity and was twice as likely to seek information about depression compared with the control group. Conclusions: Patient-targeted feedback in addition to screening has a significant but small effect on depression severity after 6 months and may encourage patients to take an active role in the self-management of depression.

注册库
who.int
开始日期
2012年7月3日
结束日期
2014年5月1日
最后更新
去年
研究类型
Observational
性别
All

研究者

发起方
Bundesministerium für Bildung und Forschung Dienstsitz Berlin

入排标准

入选标准

  • Attendance in a cardiac clinic;
  • Clinical diagnosis of coronary heart disease or hypertension;
  • Age \= 18 years;
  • Sufficient language skills;
  • Informed consent

排除标准

  • Life threatening health status;
  • Severe somatic or/and psychological disorder that needs urgent treatment;
  • Acute suicidal tendency;
  • Severe cognitive or/and visual difficulties;
  • Not being able to fill out questionnaires

结局指标

主要结局

未指定

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