PACTR202404890252448招募中Unknown
A pilot pre- post trial of the feasibility, acceptability, tolerability, and efficacy of accelerated bilateral theta-burst stimulation for depression in adults with HIV in South Africa
试验速览
- 阶段
- Unknown
- 状态
- 招募中
- 入组人数
- 10
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- All
入选标准
- •Adults (= 18 years) diagnosed with HIV
- •On ART for an uninterrupted period of at least six months
- •Current comorbid MDD diagnosis confirmed by a diagnostic interview.
- •Able to attend the treatment and monitoring visits at the university campus during office hours.
- •Able to provide written informed consent.
- •For participants on psychotropic medication, a stable dose (=2 months) will be required before the pre-treatment assessment. These participants will continue with their current treatment regimens for the duration of their trial participation.
- •Participants will also be required not to engage in other interventions (i.e., psychotherapy) during the study
- •period (six weeks from pre-treatment to one-month follow-up).
排除标准
- •Known with life-threatening medical illnesses (e.g., cancer), or serious psychiatric conditions (e.g., psychosis, mania).
- •Participants with specific TMS-associated contraindications (e.g., metal implants close to the skull area or uncontrolled epilepsy) will also be excluded.
研究者
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