Augmentation of Exposure Therapy With D-Cycloserine in Patients With Agoraphobia With or Without Panic Disorder
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 73
- 试验地点
- 1
- 主要终点
- Panic- and Agoraphobia Rating Scale (PAS)
研究概览
简要总结
Since decades, D-Cycloserine (DCS, drug class: Oxazolidinone) is proven to be an effective antibiotic agent in the treatment of tuberculosis. Furthermore it takes action in the central nervous system as an partial agonist on NMDA receptors. Because of glutamate mediated neuronal long-term potentiation in long-term memory DCS has an augmenting effect on emotional learning, as it occurs in exposure therapy of anxiety disorders. In this context we use DCS in addition to exposure therapy as a part of cognitive behavioral therapy (CBT) in patients suffering from agoraphobia with or without panic disorder. Thereby DCS is applicated oral as a capsule of 50mg, on three consecutive therapy sessions.
详细描述
The present study is a multicenter study with two participating institutions: The "Klinik für Psychiatrie und Psychotherapie, Charité - Universitätsmedizin Berlin" and the "ZPHU - Zentrum für Psychotherapie am Institut für Psychologie, Humboldt-Universität zu Berlin". It is a randomized, placebo-controlled and double blind study with agoraphobic patients receiving a manualized cognitive behavioral therapy. The randomization and blindness refers to medication with an antibiotic called D-Cycloserine: One group receives D-Cycloserine after exposure sessions and the other group is treated with a placebo. The aim is to find out, whether or not D-Cycloserine augments psychotherapy outcome when administered after an exposure. Altogether, 78 patients will be treated. Before therapy, all patients receive a clinical examination to ensure that no contraindications for participating (like cardiac defects or serious central nervous system diseases) are present. In the following diagnostic sessions therapists conduct standardized assessments and after four diagnostic sessions therapy starts. All patients receive six therapy sessions, whereof three consist of exposures. When exposures are successful, D-Cycloserine or Placebo is administered afterwards. At the last therapy session another clinical examination to control several parameters is conducted. One month after therapy, two follow-up sessions with assessments take place.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •written consent (as per AMG §40 (1) 3b)
- •diagnosis of agoraphobia; severity of the disorder due to the CGI should at least be "moderately ill"
- •age: 18-75 years
- •negative pregnancy test for premenopausal women and safe contraception (Pearlindex < 1) during the study
- •accessibility (geographical vicinity) for treatment and follow-up
- •Compliance of the patient
排除标准
- •Known overreaction after taking of D-Cycloserine
- •Actual pharmacotherapy with ethionamides and/ or isoniazide
- •Judicial or regulatory hospitalization in a mental institution (as per AMG §40 (1) 4)
- •Severe psychiatric disorder like schizophrenia, addiction or dementia
- •acute suicidal tendency
- •epilepsy or other diseases concerning the CNS (e.g. brain tumor, encephalitis)
- •internal disease like severe hypertension, cardiac insufficiency, cardiac arrhythmia, severe dysfunction of liver or kidney, insulin-dependent diabetes mellitus or disorders of the hematopoiesis
- •lactation
- •changes in a psychopharmacotherapy or discontinuation of a pretreatment with psychoactive drugs less than 4 weeks previous to the begin of the study
- •disturbance of the day and night rhythm
- •disorder-specific psychotherapy
- •participation in another AMG-study during the last month previous to the inclusion in the study or during the participation in this study
研究组 & 干预措施
D-Cycloserine + CBT
Patients receiving CBT (cognitive behavioral therapy) and D-Cycloserine (3 times, 50 mg, oral) directly after an exposure
干预措施: CBT (Behavioral)
D-Cycloserine + CBT
Patients receiving CBT (cognitive behavioral therapy) and D-Cycloserine (3 times, 50 mg, oral) directly after an exposure
干预措施: D-Cycloserine (Drug)
Placebo + CBT
Patients receiving CBT (cognitive behavioral therapy) and a placebo pill (3 times, looking identical to the DCS pill) directly after an exposure
干预措施: CBT (Behavioral)
结局指标
主要结局
Panic- and Agoraphobia Rating Scale (PAS)
时间窗: Change from Baseline to Posttreatment (5 weeks)
The PAS is designed for patients with agoraphobia or panic disorder who are at least 15 years old. It can be used to determine the severity of the disorder or to examine therapeutic success. There is a self-rating and a clinician-rating version available with 14 items each, yet the items are the same in both versions. Answers are given on a five-point Likert scale from "0" to "4" with higher scores indicating a higher severity. For determination of the severity of the disorder, 13 items are summed up, only item "U" (asking if panic attacks occur expected or unexpected) is not considered, resulting in scores between 0 and 52. There are also five sub scores if only special contents are of interest: Panic attacks, agoraphobic avoidance, anticipatory anxiety, disability, and worries about health. For the present study the German version of the questionnaire is used.
次要结局
- Clinical Global Index (CGI)(Change from Baseline to Posttreatment (5 weeks) and follow-up (9 weeks))
- Beck Anxiety Inventory (BAI)(Change from Baseline to Posttreatment (5 weeks) and follow-up (9 weeks))
- Agoraphobic Cognitions, Body Sensations Questionnaire and Mobility Inventory (AKV)(Change from Baseline to Posttreatment (5 weeks) and follow-up (9 weeks))
- Anxiety Sensitivity Index (ASI)(Change from Baseline to Posttreatment (5 weeks) and follow-up (9 weeks))
- Beck Depression Inventory first revised(BDI II)(Change from Baseline to Posttreatment (5 weeks) and follow-up (9 weeks))
- Brief Symptom Inventory (BSI)(Change from Baseline to Posttreatment (5 weeks) and follow-up (9 weeks))
研究者
Prof. Dr. Andreas Ströhle
assistant medical director
Charite University, Berlin, Germany