RTMS Feasibility Study on Adolescent Depression Stimulation
- Conditions
- Major Depressive DisorderUnipolar DepressionBipolar Depression
- Interventions
- Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
- Registration Number
- NCT06126198
- Lead Sponsor
- Uppsala University
- Brief Summary
This is an open-label study, in which all participants receives an active treatment with repetitive transcranial magnetic stimulation (rTMS) according to clinical protocol. The aim with this pilotstudy is to investigate the feasibility to perform a trial of low-frequency rTMS on treatment-resistant depression in adolescents. The study includes adolescents 13-19 years old, with average to severe depression.
- Detailed Description
The intervention follows the identical clinical procedure used for adults. Initially, the resting motor threshold will be determined by stimulation over the motor cortex, by finding the minimal intensity that produces a motor response in the corresponding distal wrist muscles. The rTMS will be delivered with a powerMAG research ppTMS stimulator (Mag \& More), and a figure-of -eight coil, PMD70-pCool (Mag \& More). The intervention is within the intended use of this CE-marked medical device. The research participants will receive 1Hz rTMS with daily sessions on 20-30 consecutive week days. The magnetic pulses will be applied at 120% of the resting motor threshold with a figure-of-eight coil at a 45 degree angle towards the midline. The 1Hz rTMS protocol is applied 6 trains of 1-min duration separated by 30-sec inter-train "off" periods over the right DLPFC (F4 site 5 according to the10-20 system). The total duration of one 1 Hz rTMS session is 8 min 30 s.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
- Informed consent from parents and legal guardian
- Age 13-19 years
- Diagnosis of uni- or bipolar depression verified through a Mini International Neuropsychiatric Interview for children and adolescents (MINI-KID)
- Treatment with at least two SSRIs at an adequate dose for at least 8 weeks
- Epilepsy or medical history of seizures
- Conductive ferromagnetic or other magnetic sensitive metals implanted in the head or within 30 cm of the treatment coil
- Implanted device that is activated or controlled in any way by physiological signals
- Implanted medication pumps
- Intracardiac lines (even if removed)
- Active substance use disorder
- Treatment with any medication that could lower the threshold for seizures
- Usage of benzodiazepines both as prescribed drug and illegal use
- Any condition that seriously increases the risk of non-compliance or loss of follow-up
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Active treatment Repetitive Transcranial Magnetic Stimulation (rTMS) Active treatment with Repetitive Transcranial Magnetic Stimulation (rTMS) according to clinical protocol.
- Primary Outcome Measures
Name Time Method Inclusion rate - two years Participant inclusion during the course of the study
Attrition rate two years Participant drop-off during the course of the study
- Secondary Outcome Measures
Name Time Method CGAS (Children's Global Assessment Scale) score 4 weeks, 6 weeks Children's Global Assessment Scale, score 1-100, where a high score indicates high functioning.
MADRS (Montgomery and Asberg Depression Rating Scale) score at Baseline, 4 weeks, 6 weeks Montgomery and Asberg Depression Rating Scale, score 0-60, where a high score indicates symtoms of depression.
Trial Locations
- Locations (1)
Uppsala University
🇸🇪Uppsala, Sweden