Depression Severe

4

Review clinical trials related to Depression Severe. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Brain Stimulation for Severe Depression

Chronic intracalvarial cortical stimulation is a minimally invasive method involving the neurosurgical placement of an electrode above the inner table of the skull. Over time, intracalvarial cortical stimulation is intermittently activated to modulate locally and distally connected brain regions. Because of the important role played by the dorsolateral prefrontal cortex in mood regulation, the goal of this study is to apply intracalvarial prefrontal cortical stimulation (IpCS) over the dorsolateral prefrontal cortex in severely treatment-resistant depressed (TRD) patients. Per the DSM-V and Centre for Medicare and Medicaid Services (CMS) nomenclatures, TRD patients are commonly defined as those whose treatment failed to produce response or remission after 2 or more attempts of sufficient duration and treatment dose. In the investigator's study, eligible TRD subjects will have a diagnosis of major depressive disorder with a suboptimal response to an adequate dose and duration of at least two different antidepressant treatment categories. These subjects will also have had exposure and transiently (non-durably) responded to non-invasive neurostimulation. The investigator anticipates that severely Treatment Resistant Depressed (TRD) Subjects with IpCS of the dorsolateral prefrontal cortex will show a significant decrease in depression symptoms as measured by the Montgomery-Asberg Depression Rating Scale (MADRS) at four months post-implant when compared to baseline. The investigator will enroll up to 20 subjects with severe refractory depression in an open trial, followed for up to one year. Depressive and cognitive symptoms will be rated periodically to assess the safety and efficacy of this procedure.

Participants needed: 20
Trial details
Age: 21-80Biological sex: AllType: InterventionalSponsor: Inner Cosmos IncUpdated: Apr 15, 2026Locations: 2
Eligibility criteria

Subject has a diagnosis of chronic (≥ two years) or recurrent (multiple prior ep... [+7]

The IpCS would (in the investigator's judgment) pose an unacceptable surgical or... [+10]

Status: Recruiting

Telehealth Behavioral Activation for Teens

Behavioral activation is one such empirically supported intervention. Derived from cognitive-behavioral therapy, a well-established treatment for depression, behavioral activation uses psychoeducation and skill-building to increase an individual's engagement in valued and enjoyable activities (e.g., socializing with family and friends, exercising, participating in a hobby) in order to improve depressive symptoms. Research has shown that behavioral activation is an effective intervention for depressed youth. Additionally, it has been shown as a promising intervention that can be conducted in a brief, virtual format and can be effectively implemented by both trained clinicians and trained, non-licensed interventionists. This project will provide Behavioral Activation for youth (12-17) experiencing depression or suicidal ideation who are currently enrolled in the Youth Depression Suicide Network study in Texas.

Participants needed: 250
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Baylor College of MedicineUpdated: Jul 20, 2025Locations: 1
Eligibility criteria

Participants must be enrolled in the Texas Youth Depression Suicide Research Net... [+9]

Have an acute medical or psychological condition(s) that that would, in the judg... [+3]

Status: Recruiting

Kintsugi Voice Device Pivotal Study

A prospective, single arm, non-randomized, pivotal clinical validation study to evaluate the ability of the Kintsugi Voice Device (the Device) to aid clinical assessment for depression by comparing its output with a diagnosis made by a clinician using the Structured Clinical Interview for DSM-5 (SCID-5-RV) for up to 1000 English speaking adult patients ages 22 and older living in the United States. Recruitment will occur for 1 year and participation will be for up to 2 weeks

Participants needed: 1,000
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: Kintsugi Mindful Wellness, Inc.Updated: Apr 30, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Integrated Depression Care

The Integrated DEpression CAre (IDECA) Programme is a multi-faceted intervention strategy aiming to improve guideline adherence and shared care practices for depression management in both providers and patients, as measured through a set of process and clinical outcome indicators (primary outcome measure).

Participants needed: 150
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University GhentUpdated: Jun 6, 2024Locations: 2
Eligibility criteria

persons between 18-65 [+2]

Severe depression warranting direct referral to specialized services