Studies brain stimulation and heart rate changes in people with treatment-resistant depression
Tests repetitive magnetic brain stimulation in adults with treatment-resistant depression.
Plain-language title generated from the registry record
Registry title: Neurocardiac Predictors of Treatment Response to RTMS in Depression
Key facts
- Where
- Vancouver, CanadaSee the site
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 19 and 65 years old?
Source: NCT05139862, who can take part
Where in Canada
- Non-Invasive Neurostimulation Therapies (NINET) Laboratory, UBC Department of PsychiatryVancouver, CanadaNo longer taking part
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- University of British Columbia
- Trial code
- NCT05139862
- Record updated
- 24 December 2024
- Original description
Heartbeat is controlled by the brain and is regular but flexible to change in response to environmental and internal stimuli. This feature is known as heart rate variability (HRV). Major depressive disorder (MDD) has been associated with diminished HRV and this is a reflection of abnormal brain function caused by MDD. Repetitive transcranial magnetic stimulation (rTMS) is a treatment that stimulates specific areas of the brain. The goal of this study is to test the hypothesis that rTMS induces changes in connectivity between the area of the brain stimulated with rTMS and deeper areas in the brain associated to heart rate regulation. 110 patients with TRD will be recruited and will undergo a concurrent TMS-fMRI session before receiving a course of iTBS to the L-DLPFC for 30 sessions at 120% rMT.Read full original descriptionShow less
Neuro-cardiac Predictors of Treatment Response to RTMS in Depression: a Mechanistic Study Using Interleaved TMS-fMRI
Heartbeat is controlled by the brain and is regular but flexible to change in response to environmental and internal stimuli. This feature is known as heart rate variability (HRV). Major depressive disorder (MDD) has been associated with diminished HRV and this is a reflection of abnormal brain function caused by MDD. Repetitive transcranial magnetic stimulation (rTMS) is a treatment that stimulates specific areas of the brain. The goal of this study is to test the hypothesis that rTMS induces changes in connectivity between the area of the brain stimulated with rTMS and deeper areas in the brain associated to heart rate regulation. 110 patients with TRD will be recruited and will undergo a concurrent TMS-fMRI session before receiving a course of iTBS to the L-DLPFC for 30 sessions at 120% rMT.
Inclusion: Patients will be included if they:; are female or male; are outpatients; are voluntary and competent to consent to treatment; have a DSM 5 diagnosis of MDD, single or recurrent confirmed by Mini-International Neuropsychiatric Interview (MINI) version 6.0; are between the ages of 18 and 65 years; have failed to achieve a clinical response to an adequate dose of an antidepressant based on an Antidepressant Treatment History Form (ATHF) score of > 3 in the current episode OR have been unable to tolerate at least two separate trials of antidepressants at less than the minimum adequate dose and/or duration (ATHF 1 or 2); A score ≥ 18 on the Hamilton Depression Rating Scale (HDRS-17 item); Have had no increase or initiation of any psychotropic medication in the 4 weeks prior to screening; Able to adhere to the treatment schedule; pass the TMS and MRI adult safety screening questionnaires.
Exclusion: have a concomitant major unstable medical illness; have previously received rTMS; have any intracranial implant (e.g., aneurysm clips, shunts, stimulators, cochlear implants, or electrodes) or any other metal object within or near the head, excluding the mouth, that cannot be safely removed; if participating in psychotherapy, must have been in stable treatment for at least 3 months prior to study entry, with no anticipated change in the frequency of therapeutic sessions, or focus of therapeutic sessions over the duration of the study; are currently taking lorazepam greater than 2 mg daily (or equivalent) or any dose of an anticonvulsant, due to the potential to limit rTMS efficacy; have failed more than three adequate trials (ATHF > 3) of medication in the current episode; have a history of substance use within the last 3 months; have a lifetime (MINI) diagnosis of any psychotic or bipolar disorder; have a MINI anxiety disorder or personality disorder assessed by a study investigator to be primary and causing greater impairment than MDD; have any significant neurological disorder, any history of seizure (except those therapeutically induced by ECT), significant head trauma with loss of consciousness for > 5 min; have a non-correctable clinically significant sensory impairment (i.e., cannot hear well enough to cooperate with interview); have a clinically significant laboratory abnormality, in the opinion of the one of the principal investigators; Patients are excluded if they:; have active suicidal intent; are pregnant; have ever failed a course of ECT.