DRKS00030936招募中Unknown
Research project to test the efficacy of an online follow-up program for patients with anxiety disorder using randomized controlled designs
Sympatient GmbH0 个研究点目标入组 414 人开始时间: 2022年12月14日最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 发起方
- 入组人数
- 414
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 80 Years（—）
- 性别
- All
入选标准
- •? Presence of a primary diagnosed anxiety disorder (for RCT-A: agoraphobia with/without panic disorder F40.0-/6B32; for RCT-P: panic disorder F41.0/6B34; for RCT-S: social phobia F40.1/6B34).
- •? Current, at least mild, anxiety symptomatology as measured by a summed score of at least 30 on the LSAS for the RCT-S, or at least 8 on the PAS for the RCT-A and RCT-P at the time of baseline interview (T0)
- •? One prior psychotherapeutic treatment for the anxiety disorder completed within the past 12 months
- •? No current medication for the anxiety disorder or medication stable for at least 4 weeks before inclusion
- •? Presence of internet access and a device to use Invirto Aftercare.
- •? Sufficient understanding of the German language
- •? Willingness to use Invirto Nachsorge on their own responsibility.
排除标准
- •?Acute suicidality
- •?Current ongoing psychotherapeutic treatment at baseline assessment
- •?Diagnosis of schizophrenic or bipolar disorder
- •?Contraindication to the Invirto aftercare medical device
研究者
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