PACTR202404890252448RecruitingUnknown
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
Faculty of Medicine and Health Sciences0 sites10 target enrollmentStarted: March 28, 2024Last updated:
Trial Snapshot
- Phase
- Unknown
- Status
- Recruiting
- Enrollment
- 10
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 19 Year(s) to 44 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •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).
Exclusion Criteria
- •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.
Investigators
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