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临床试验/NCT05385614
NCT05385614Unknown不适用

Efficacy of Gamified Cognitive Control Training Using de:)Press on Depression Severity add-on to Treatment as Usual

University Hospital Tuebingen1 个研究点 分布在 1 个国家目标入组 112 人开始时间: 2022年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
112
试验地点
1
主要终点
MADRS

研究概览

简要总结

Depression is one of the most frequent and devastating psychiatric diseases with a substantial bur-den for patients and society. It is specifically associated with dysfunctional activity in brain networks subserving cognitive control of emotional information processing. Normalization of this activity is a hallmark of various treatment approaches. Computerized training of cognitive control has shown antidepressant effects in experimental lab settings and small clinical pilot trials. However, motiva-tion, treatment adherence, and access for patients are major challenges that limit its broader use. To address these challenges, we developed a software application (de:)press®) that integrates gamification elements in a standard cognitive control task to support motivation, usage time, usabil-ity, and therefore symptom reduction. In a previous pilot trial, we were able to document that de:)press® is superior to a non-gamified standard cognitive control training in reducing depression symptomatology. Based on these data, we now designed a full-size confirmatory trial for the pur-pose of testing the hypothesis that de:)press® provides a positive healthcare effect by means of reduction in depression severity compared to treatment as usual (TAU). In this randomized, con-trolled, clinical trial 112 patients will be randomized to the intervention group (IG) with de:)press® additional to TAU, or the control group (CG) receiving only TAU. For a period of 6 weeks, the IG is provided with de:)press®. To prove a stable efficacy of de:)press®, the primary endpoint is the dif-ference in the Montgomery-Åsberg Depression Scale (MADRS) change 4 weeks after the end of training between IG and CG.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Participant, Investigator, 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
否

入选标准

  • •Male, female, diverse,
  • •age >= 18,
  • •informed consent,
  • •sufficient understanding of German (native speaker or CEFR level B skills or higher),
  • •unipolar depression diagnosed according to ICD-10 (F32.0, F32.1, F32.2 or F
  • •0, F32.1, F32.2).
  • •consultation with a physician due to depressive symptomatology within the last 6 months

排除标准

  • •Inability to give consent,
  • •inability to use de:)press® on a tablet or smartphone,
  • •acute suicidality,
  • •schizophrenia (F20),
  • •brief psychotic disorder (F23),
  • •schizoaffective disorder (F25),
  • •mental disorders due to known physiological conditions (F00 - F09),
  • •major depressive disorder, single episode, severe with psychotic features (F32.3),
  • •major depressive disorder, recurrent, severe with psychotic features (F33.3),
  • •Intellectual disability (F70 - F79).

研究组 & 干预措施

Control

No Intervention

Control group that will receive the app after primary endpoint was assessed.

Intervention

Experimental

Experimental group that will receive the app at the start of their participation

干预措施: de:)press (Behavioral)

结局指标

主要结局

MADRS

时间窗: 10 weeks

Difference in symptom severity-reduction (MADRS) between IG and CG at the final examination.

次要结局

  • Training sessions(6 weeks)
  • Response rate(10 weeks)
  • IDS-SR reduction(10 weeks)
  • WHO-5 changes(10 weeks)
  • Remission rate(10 weeks)
  • Self-esteem(10 weeks)
  • WPAI changes(10 weeks)
  • Adverse events(10 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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