跳至主要内容
临床试验/NCT03988985
NCT03988985已完成不适用

Enhancing the Clinical Effectiveness of Depression Screening Using Patient-targeted Feedback in General Practices: The GET.FEEDBACK.GP Multicentre Randomized Controlled Trial

Universitätsklinikum Hamburg-Eppendorf10 个研究点 分布在 1 个国家目标入组 1,030 人开始时间: 2019年7月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,030
试验地点
10
主要终点
Depression severity (Questionnaire: Patient Health Questionnaire-9)

研究概览

简要总结

The multi-center GET.FEEDBACK.GP randomized controlled trial is designed based on patients' needs and preferences. In order to evaluate the effect of feedback in the broader setting of primary care, a total of 1076 primary care patients with elevated levels of depression (PHQ-9 score ≥ 10) will be randomized into three groups who either receive a) patient-targeted and physician-targeted feedback of depression screening results, b) a physician-targeted feedback of depression screening results only, or c) no feedback of screening results. The primary study outcome is depression severity after 6 months, secondary outcomes include the patients' behavior and cognitions after the screening, depression care according to German guideline recommendations and the health economic evaluation.

详细描述

Major depression is one of the most significant clinical disorders. In primary care, every sixth patient suffers from increased depression level, which is associated with higher risk of suicide, increased risk of onset and progression of chronic physical conditions. Still, depression is under recognized and undertreated in primary care. Moreover, evidence regarding the efficacy of depression screening in primary care is insufficient to draw clear conclusions. Our previous mono-center depression screening trial in cardiac patients, provides first evidence that written patient-targeted feedback improves depression severity, encourages greater patient participation and engagement in mental health. To amplify these effects, the multi-center GET.FEEDBACK.GP randomized controlled trial is now designed based on patients' needs and preferences. In order to evaluate the effect of feedback in the broader setting of primary care, a total of 1076 primary care patients with elevated levels of depression (PHQ-9 score ≥ 10) will be randomized into three groups who either receive a) patient-targeted and physician-targeted feedback of depression screening results, b) a physician-targeted feedback of depression screening results only, or c) no feedback of screening results. The primary study outcome is depression severity after 6 months, secondary outcomes include the patients' behavior and cognitions after the screening, depression care according to German guideline recommendations and the health economic evaluation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Screening
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Gender: male, female, diverse
  • Maximum Age: no maximum age
  • Attendance in primary care with medical consultation
  • Age ≥ 18 years;
  • Sufficient language skills;
  • Informed consent
  • Patient Health Questionnaire-9 > 9 points

排除标准

  • Life threatening health status;
  • Severe somatic or/and psychological disorder that needs urgent treatment;
  • Known diagnosis of a depressive disorder
  • Current depression treatment
  • Acute suicidal tendency;
  • Severe cognitive or/and visual difficulties;
  • Not being able to fill out questionnaires
  • No contact details

结局指标

主要结局

Depression severity (Questionnaire: Patient Health Questionnaire-9)

时间窗: Six months after screening

Level of depression severity six months after screening (Patient Health Questionnaire-9)

次要结局

  • Depression severity (Questionnaire: Patient Health Questionnaire-9)(One and twelve months after screening)
  • Anxiety (Questionnaire: Generalized Anxiety Disorder-7)(One, six and twelve months after screening)
  • Health economic Evaluation (Questionnaire: Client Sociodemographic and Service Receipt Inventory)(Six and twelve months after screening)
  • Somatic symptom severity (Questionnaire: Somatic Symptom Scale-8)(One, six and twelve months after screening)
  • Depression treatment(Six and twelve months after screening)
  • Quality-adjusted life years (Questionnaire: EuroQol-5D)(Six and twelve months after screening)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (10)

Loading locations...

相似试验