IRCT20240713062416N1尚未招募Unknown
Effectiveness of repeated transcranial magnetic stimulation on sleep quality, emotional disturbance and severity of disorder symptoms in patients with emotional disorders
Islamic Azad University Semnan branch0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- Unknown
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 65 years(—)
- 性别
- All
入选标准
- •Patients must be certified by a psychiatrist or psychologist based on DSM-5 or ICD-10 diagnostic criteria.
- •The age range of participants should be between 18 and 65 years.
- •Patients must have moderate to severe symptom severity as assessed using validated instruments such as the Beck Depression Scale (BDI), Hamilton Anxiety Scale (HAM-A), or similar instruments.
- •Patients must sign informed consent and be willing to participate in all repeated transcranial magnetic stimulation sessions and related assessments.
- •Patients who are currently receiving medication or psychotherapy should have stable treatment and not have any major changes in their treatment for at least 4 weeks before the start of the study.
- •Patients must have significant problems in sleep quality and emotional disturbances that affect their quality of life and daily performance.
排除标准
- •Patients diagnosed with other psychiatric disorders such as psychotic disorders, bipolar disorders or substance abuse disorders in the period of 6 months before the start of the study.
- •Taking medications that may interfere with transcranial magnetic stimulation, such as anticonvulsants or antipsychotics.
- •Patients with serious physical problems such as cardiovascular disease, renal or hepatic failure, or serious neurological disease that may interfere with the treatment protocol.
- •Patients with metal implants in the head or neck area (such as implanted hearing aids) that may be stimulated by magnetic fields.
- •Pregnant or lactating women due to unknown risks to the fetus or infant.
- •Patients who do not attend or follow instructions for repeated transcranial magnetic stimulation sessions or follow-up assessments.
- •Patients who decide to withdraw from the study at any stage of the research and do not want to continue.
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