jRCT1030250720招募中不适用
Development and Preliminary Evaluation of the Efficacy and Safety of Video-Assisted Group Cognitive Behavioral Therapy for Obsessive-Compulsive Disorder (VOCT)
未提供0 个研究点目标入组 15 人开始时间: 待定
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 15
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
- Single Arm Study
入排标准
- 年龄范围
- 18age old over 至 65age old under(—)
- 性别
- All
入选标准
- •Age 18 or older at the time of consent acquisition
- •Diagnosed with obsessive-compulsive disorder by a primary physician and currently undergoing treatment
- •Permission to participate in this study is obtained from the primary physician
- •Able to respond to interviews online
- •Understands the purpose and content of this study and provides written informed consent to participate voluntarily
- •Consent to not share the program and its materials developed by the research team with others
- •Aged 18 years or older and 65 years or younger at the time of consent acquisition
- •Currently receiving outpatient treatment at this hospital for a diagnosis of obsessive-compulsive disorder
- •Y-BOCS-SR score of 8 points or higher
- •Has obtained permission from their primary physician to participate in this study
- •Understands the purpose and content of this study and has provided written informed consent to participate voluntarily
排除标准
- •Individuals deemed unsuitable for this study by the principal investigator
- •Individuals exhibiting significant suicidal ideation at the pre-intervention assessment stage
- •Individuals exhibiting significant manic episodes at the pre-intervention assessment stage
- •Individuals for whom weekly attendance during the intervention period is known to be difficult in advance
- •Individuals scheduled to receive other structured psychotherapy (excluding supportive therapy) during the intervention period
- •Individuals with physical illness or severe cognitive impairment at the pre-intervention assessment point that would make participation in group cognitive behavioral therapy difficult
- •Individuals who received treatment with structured psychotherapy, modified electroconvulsive therapy, or transcranial magnetic stimulation (excluding medication) within 3 months prior to the pre-intervention assessment.
- •Individuals with difficulty accessing the internet or operating basic digital devices.
- •Other individuals deemed unsuitable for this study by the principal investigator.
研究者
相似试验
尚未招募
Unknown
Efficacy of a web-based virtual clinic in the treatment of sexual dysfunction and the enhancement of the sexual quality of life for couples.Sexual dysfunctionIRCT20110827007422N5Mashhad University of Medical Sciences80
尚未招募
不适用
A Randomized Controlled Trial to Evaluate the Effect of a Senior-targeted SNS "Oshiruco" on Social Frailty among Older Adultsfrailty
social frailtyfrailty social frailtyjRCT1022250034100
招募中
2 期
Development, Validation and Evaluation of the Effectiveness of the native Spiritual Care Protocol Based on Iranian-Islamic Culture in Advance Cancer Patients and Their Caregiversadvance cancer.Malignant neoplasm without specification of siteIRCT20220509054792N1Iran University of Medical Sciences5
招募中
1 期
Prospective feasibility pilot study evaluating the value of [68Ga]Ga-PENTIXAFOR PET-CT in patients with metastatic Small Cell Lung Cancer (SCLC) at diagnosis and disease progression (PASSIFLORE)2024-514057-30-00Institut De Cancerologie De L Ouest15
招募中
3 期
Acceptance Based Emotion Regulation Group Intervention in Type 1 Bipolar PatientsIRCT20240217061031N1Artesh University of Medical Sciences36
