Clinical Trials for Depression

Currently registered clinical trials for Depression from ClinicalTrials.gov. 27 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Depression from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 27
  • Active, not recruiting: 2
  • Completed: 16
  • Other: 5

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT02543983 — Neurobiology of Suicide

StatusRecruiting
PhasePhase 2
SponsorNational Institute of Mental Health (NIMH)
Enrollment325
Study TypeINTERVENTIONAL
ConditionsHealthy Volunteers; Depression
Interventions; ;

Background:

There are no good treatments for people considering suicide. Researchers want to study suicide with questions, blood tests, brain imaging, and sleep studies. They hope to better understand suicide, so they can help suicidal people.

Objective:

To understand what happens in the brain when someone has thought about or attempted suicide.

Eligibility:

Group 1: Adults ages 18 70 who …

StatusRecruiting
PhaseN/A
SponsorNational Institute on Drug Abuse (NIDA)
Enrollment620
Study TypeINTERVENTIONAL
ConditionsMajor Depressive Disorder; Substance Use Disorder; Normal Physiology
Interventions;

Background:

Nicotine dependence leads to about 480,000 deaths every year in the United States. People with major depressive disorder (MDD) are twice as likely to use nicotine compared to the general population. They have greater withdrawal symptoms and are more likely to relapse after quitting compared with smokers without MDD. More research is needed on how nicotine affects brain function in …

NCT05660642 — An Open-Label Study to Evaluate the Safety, Tolerability and Pharmacodynamics of BPL-003 in Patients With Treatment Resistant Depression

StatusRecruiting
PhasePhase 2
SponsorBeckley Psytech Limited
Enrollment72
Study TypeINTERVENTIONAL
ConditionsTreatment Resistant Depression
Interventions

An open-label, multi-centre, Phase 2a study to evaluate the safety, tolerability, and pharmacodynamics of one and two doses of intranasal BPL-003 combined with psychological support, in patients with treatment resistant depression when administered as monotherapy or as adjunctive therapy with defined SSRIs (citalopram, escitalopram, sertraline or fluoxetine).

NCT05850689 — Study of Lumateperone as Adjunctive Therapy in the Treatment of Patients With Major Depressive Disorder

StatusRecruiting
PhasePhase 3
SponsorIntra-Cellular Therapies, Inc.
Enrollment470
Study TypeINTERVENTIONAL
ConditionsMajor Depressive Disorder
Interventions;

This is a multicenter, randomized, double-blind, placebo-controlled parallel-group, fixed-dose study in patients with a primary diagnosis of MDD according to criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) who have an inadequate response to ongoing ADT.

NCT06372964 — Multicenter Study of Lumateperone for the Treatment of Bipolar Depression in Pediatric Patients

StatusRecruiting
PhasePhase 3
SponsorIntra-Cellular Therapies, Inc.
Enrollment384
Study TypeINTERVENTIONAL
ConditionsBipolar Depression
Interventions;

This is a multicenter, randomized, double-blind, placebo-controlled study in pediatric patients who are experiencing major depressive episodes (MDEs) associated with a primary diagnosis of bipolar I or bipolar II disorder as confirmed by Kiddie Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL), according to criteria of the Diagno…

NCT06445933 — Vitamin B6 and Depression in Pregnant and Peri-partum Women

StatusRecruiting
PhaseN/A
SponsorNational Taiwan University Hospital
Enrollment150
Study TypeINTERVENTIONAL
ConditionsPostpartum Depression; Heart Rate Variability
Interventions;

Perinatal depression is a highly prevalent and serious health issue during pregnancy. According to statistics, approximately one out of every ten postpartum women experiences this condition. Symptoms can manifest as mood fluctuations or emotional lows. Unfortunately, these symptoms are often overlooked by patients themselves or misinterpreted by others as normal adjustments to the new role of m…

NCT06559306 — Phase 3 Study of Adjunctive Treatment With Seltorexant in Adult and Elderly Participants With Major Depressive Disorder and Insomnia Symptoms

StatusRecruiting
PhasePhase 3
SponsorJanssen Research & Development, LLC
Enrollment752
Study TypeINTERVENTIONAL
ConditionsDepressive Disorder, Major
Interventions; ;

The purpose of this study is to know how well seltorexant works, and also to evaluate safety and maintenance effect of seltorexant compared with placebo as an adjunctive therapy to an antidepressant in improving depressive symptoms in participants with major depressive disorder with insomnia symptoms (MDDIS) who have had an inadequate response to current antidepressant therapy with a selective …

NCT06049888 — Does Social Media Impact Adolescent Mental Health?

StatusRecruiting
PhaseN/A
SponsorGeorgetown University
Enrollment500
Study TypeINTERVENTIONAL
ConditionsMental Health
Interventions

The mental health of adolescents in the United States has seen a steep decline, roughly coinciding with the increasing popularity of social media and smartphones. But does social media have a causal impact on the mental health of adolescents or are concerns about the effect of social media on kids a form of public hysteria? In this study, the investigators will conduct the first field experimen…

NCT06547489 — Zelquistinel or Placebo for the Reduction of Symptoms of Major Depressive Disorder

StatusRecruiting
PhasePhase 2
SponsorSyndeio Biosciences, Inc
Enrollment164
Study TypeINTERVENTIONAL
ConditionsMajor Depressive Disorder
Interventions

The goal of this clinical trial is to learn if zelquistinel works to treat depression in adults. It will also learn about the safety of zelquistinel. The main questions it aims to answer are:

Does zelquistinel reduce depression scores in participants compared to participants who take a placebo (a look-alike tablet that contains no zelquistinel)?

What medical problems are observed in participa…

NCT06384196 — Identity-Based Transdiagnostic Therapy for Young People With Anxiety and Depression

StatusRecruiting
PhaseN/A
SponsorUniversity of Barcelona
Enrollment138
Study TypeINTERVENTIONAL
ConditionsDepression; Anxiety
Interventions;

Depression and anxiety are the most prevalent mental disorders among both the general population and young adults, and transdiagnostic treatments for these patients are mostly based on cognitive-behavioral therapy (CBT). Based on common (transdiagnostic) principles of treatment (e.g., emotional exposure), these approaches have proliferated and demonstrated their efficacy in comparison to disord…

NCT07048574 — TIDES 2.0: Prevalence and Longitudinal Course of Depression, Anxiety, and Behavior Problems in Children With Cystic Fibrosis Under 12 Years of Age

StatusRecruiting
PhaseN/A
SponsorState University of New York at Buffalo
Enrollment600
Study TypeOBSERVATIONAL
ConditionsCystic Fibrosis (CF)

This is a longitudinal, observational epidemiological study designed to estimate the prevalence of depression, anxiety, and behavior problems in children ages 18 months through 11 years with cystic fibrosis (CF).

NCT07113067 — Accelerated rTMS vs. Sham for Stroke Apathy

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorMedical University of South Carolina
Enrollment40
Study TypeINTERVENTIONAL
ConditionsApathy; Stroke; Stroke Sequelae; Stroke/Brain Attack; Stroke/ Cerebrovascular Accident (Ischemic or Hemorrhagic)
Interventions; ;

Apathy is a common set of symptoms seen in many people following a stroke. Apathy occurs when a person has lost motivation, becomes withdrawn, and stops doing things that used to be important to them. Apathy has a large negative impact on a person’s quality of life, and can also have a large impact the people who take care of them. There are currently no FDA-approved treatments to help with apa…

NCT06188923 — A New Intervention to Improve Function in Veterans With Anxiety and Depression

StatusRecruiting
PhasePhase 2
SponsorVA Office of Research and Development
Enrollment84
Study TypeINTERVENTIONAL
ConditionsAnxiety and Depression
Interventions;

Anxiety and depression symptoms occur at high rates in Veteran populations and can significantly impact function, compromising the ability to work and to successfully form and maintain valued relationships. Several other symptoms commonly occur with anxiety and depression, including poor sleep quality and chronic pain. Since all these symptoms frequently occur together, they may have a common u…

NCT07687940 — Feasibility and Effects of a Blended Baduanjin Exercise and Green Tea Consumption Program on Depressive Symptoms, Gut Microbiota and Quality of Life in Older Adults

StatusRecruiting
PhaseN/A
SponsorHong Kong Baptist University
Enrollment48
Study TypeINTERVENTIONAL
ConditionsDepressive Symptoms
Interventions;

Depression is a common mental health issue in older adults, often manifesting as insomnia, low mood, vague somatic complaints, cognitive decline, and recurrent thoughts of death or suicide. Even subthreshold depressive symptoms in late life significantly impair quality of life. In Hong Kong, recent data show high prevalence of depressive symptoms among community-dwelling older adults (43.7% in …

NCT06926296 — Moral Injury in French Healthcare Workers

StatusRecruiting
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment3073
Study TypeINTERVENTIONAL
ConditionsMoral Injury
Interventions

Healthcare professionals are facing an escalating crisis, with burnout rates ranging between 40% and 60% and a growing intention to leave the profession, affecting one in five physicians and one in four nurses in the coming years. While current interventions focused on individual resilience, such as mindfulness, peer support, and workload management, have been promoted as solutions, they have f…

NCT07691411 — An Ecological Momentary Assessment Based Program to Support Self-Management for Post-stroke Patients

StatusRecruiting
PhaseN/A
SponsorThe Hong Kong Polytechnic University
Enrollment50
Study TypeINTERVENTIONAL
ConditionsStroke; Post Stroke
Interventions

The goal of this feasibility study is to test whether a new approach that combines real-time symptom tracking (Ecological Momentary Assessment) with machine learning can help people recovering from a stroke to better manage depression, thinking difficulties, and daily functioning. The main questions it aims to answer are:

Is this combined approach practical and acceptable for post-stroke survi…

NCT06389565 — Change My Story Task Shifted Mental Health Intervention

StatusRecruiting
PhaseN/A
SponsorMassachusetts General Hospital
Enrollment80
Study TypeINTERVENTIONAL
ConditionsHiv; Depression; Psychological Distress
Interventions;

Psychological distress and depression are common among young people living with HIV (Y-PLWH) and negatively impact medication adherence and disease control. In low- and middle-income countries, this problem is compounded by the lack of trained mental health professionals on the provider side and the requirement of frequent clinic-based visits imposing greater cost, inconvenience, and stigma for…

NCT06696755 — A Study to Assess Adverse Events and Change in Disease Activity of Oral Icalcaprant in Adult Participants With Bipolar I or II Disorder

StatusRecruiting
PhasePhase 2
SponsorAbbVie
Enrollment195
Study TypeINTERVENTIONAL
ConditionsBipolar I Disorder; Bipolar II Disorder
Interventions;

Bipolar disorder is a severe chronic mood disorder that affects up to 4% of the adult population and 1.8% of the pediatric population in the United States. This study will assess how safe and effective Icalcaprant is in treating adult participants with bipolar I or II disorder.

Icalcaprant is an investigational drug being developed for the treatment of depressive episodes in adult participants…

NCT07412756 — A Study of Brenipatide in Adult Participants With Major Depressive Disorder

StatusRecruiting
PhasePhase 3
SponsorEli Lilly and Company
Enrollment1000
Study TypeINTERVENTIONAL
ConditionsDepressive Disorder, Major
Interventions;

This study evaluates the safety and efficacy of brenipatide when administered with standard of care (SoC) compared to placebo plus SoC in delaying the return of major depressive symptoms.

The trial is divided into three periods as follows: a screening period that will last approximately 1 month, a treatment period that will last a minimum of 12 months, and the follow up period that will last a…

NCT07508215 — Efficacy of Bright Light Therapy on Cognitive Impairment in Major Depressive Disorder and Its Neuroimaging Mechanisms: Protocol for a Randomised Controlled Trial

StatusRecruiting
PhaseN/A
SponsorPeking University Sixth Hospital
Enrollment120
Study TypeINTERVENTIONAL
ConditionsMajor Depressive Disorder (MDD); Neuroimaging; Bright Light Treatment; Cognitive Impairment
Interventions;

This study aims to validate the therapeutic efficacy and safety of bright light therapy (BLT) in ameliorating cognitive impairment (CI) in major depressive disorder (MDD), characterize the functional and structural features of the hippocampus (HPC)-dorsolateral prefrontal cortex (dlPFC) neural circuitry in MDD participants with CI and examine the mediating effect of the HPC-dlPFC neural circuit…

NCT07686718 — To Establish Whether Individuals With Premenstrual Dysphoric Disorder (PMDD) Demonstrate a Different Luteal-phase Sex Hormone Profile and Ratio Compared With Asymptomatic Controls.

StatusRecruiting
PhaseN/A
SponsorLancaster University
Enrollment50
Study TypeOBSERVATIONAL
ConditionsPremenstrual Dysphoric Disorder ( PMDD)

The aim of this project is to compare the ovarian hormone levels 7 days after ovulation and progesterone:oestradiol ratios between PMDD individuals and a control cohort (case control study).

NCT07688720 — Transcutaneous Auricular Neurostimulation (tAN) for Premenstrual Dysphoric Disorder (PMDD) and Perimenopause

StatusRecruiting
PhaseN/A
SponsorTexas Christian University
Enrollment20
Study TypeINTERVENTIONAL
ConditionsPerimenopause; PMDD
Interventions

Transcutaneous Auricular Neurostimulation (tAN) will be administered to women with premenstrual syndrome (PMS), premenstrual dysphoric disorder (PMDD), and perimenopause. The investigators will examine whether tAN improves symptomology by collecting self-report data before the intervention, during the intervention, and following the intervention.

NCT07224165 — Developing a Digital Intervention for Adolescent Nonsuicidal Self-injury

StatusRecruiting
PhaseN/A
SponsorNorthwestern University
Enrollment80
Study TypeINTERVENTIONAL
ConditionsNonsuicidal Self-injury; Depression; Anxiety
Interventions;

This is a feasibility trial of a digital mental health intervention aimed at adolescents (ages 14-18) with nonsuicidal self-injury and who are not currently engaged in mental health treatment. The study has two arms: a self-guided DMHI and an active control which will involve the delivery of non-interactive psychoeducational content via the same app interface. The primary goals of this project …

NCT07684911 — Longitudinal Study on the Sustainability of Transcranial Magnetic Stimulation Protocols - Biomarkers

StatusRecruiting
PhaseN/A
SponsorHospital Center Guillaume Régnier
Enrollment30
Study TypeOBSERVATIONAL
ConditionsDepression - Major Depressive Disorder; Depression Bipolar; Depression Unipolar
Interventions

Despite advances in the effective treatment of major depressive disorder using repetitive transcranial magnetic stimulation (rTMS), the processes that determine a patient’s response trajectory remain poorly understood.

Currently, there are no validated clinical or neurophysiological markers that can identify factors predicting the durability of the response to rTMS at the individual level. Thi…

NCT07611773 — EEG Prediction and Clinical Efficacy of tDCS in Major Depression

StatusRecruiting
PhaseN/A
SponsorIonclinics & Deionic SL
Enrollment270
Study TypeINTERVENTIONAL
ConditionsDepression - Major Depressive Disorder
Interventions;

The purpose of this randomized controlled trial is to investigate the non-inferiority, and possible superiority, of a high-dose home-based tDCS protocol compared with a conventional home-based protocol, and to assess its cost-effectiveness, in patients with major depression.

As a secondary aim, we aim to assess the predictive value of baseline EEG for clinical response to high-dose home-based …

NCT07682935 — Investigation of the Effects of Angling as Supportive Therapy in Schizophrenia Treatment on Serum Parameters, Anxiety, Depression, and Quality of Life

StatusRecruiting
PhaseN/A
SponsorFirat University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsAngling; Supportive Therapeutic; Schizophrenia
Interventions

This study aims to evaluate the effects of recreational fishing (angling) as a supportive therapeutic intervention in individuals diagnosed with schizophrenia. Schizophrenia is a chronic psychiatric disorder characterized by disturbances in thinking, perception, emotion, and behavior, often accompanied by negative symptoms such as social withdrawal, anhedonia, and cognitive impairment, which si…

NCT07346014 — Sleep and Circadian Interventions for College Students at High Risk of Suicide

StatusRecruiting
PhaseN/A
SponsorUniversity of Pittsburgh
Enrollment90
Study TypeINTERVENTIONAL
ConditionsSleep Disturbance; Sleep; Depression; Suicide
Interventions; ;

The purpose of this study is to examine the extent to which delivering sleep and circadian focused interventions in addition to evidenced based psychiatric care for depression and suicide risk may contribute to decreasing suicide risk among high risk young adults. Investigators will evaluate three interventions targeting sleep in acutely suicidal college students enrolled in intensive outpatien…

Active, Not Recruiting

NCT00005398 — University of North Carolina Alumni Heart Study

StatusActive, not recruiting
PhaseN/A
SponsorDuke University
Enrollment6340
Study TypeOBSERVATIONAL
ConditionsCardiovascular Diseases; Heart Diseases; Coronary Disease; Depression
Interventions

To continue surveillance of the participants in the University of North Carolina Alumni Heart Study, which tests the hypothesis that hostility and related psychosocial factors are involved in the pathogenesis of coronary heart disease.

NCT07684677 — Effect of Participating in a Study of Causes of Pregnancy Loss on Mental Health Outcomes: A Target Trial Emulation Using the COPL Cohort and Danish National Registries

StatusActive, not recruiting
PhaseN/A
SponsorAmager Hospital
Enrollment30000
Study TypeINTERVENTIONAL
ConditionsPregnancy Loss, Early; Major Depression; Anxiety; Stress (Psychology)
Interventions

Pregnancy loss is the most common severe pregnancy complication and is associated with significant mental health sequelae, including depression and anxiety. Standard care in Denmark does not include systematic follow-up or aetiological investigation after pregnancy loss. The Copenhagen Odense Pregnancy Loss (COPL) Cohort offered extensive aetiological investigations, and a dedicated clinical fo…

Not Yet Recruiting

NCT06907654 — Couples’ Affect in Relationships Study

StatusNot yet recruiting
PhaseN/A
SponsorUniversity of Wisconsin, Madison
Enrollment2000
Study TypeINTERVENTIONAL
ConditionsDepression Disorders
Interventions;

The goal of this clinical trial is to find out whether learning about well-being impacts the thoughts and feelings of romantic couples. The main question it aims to answer is:

  • Does gaining knowledge about well-being positively impact individuals and their romantic relationships?

Participants will complete online surveys about their thoughts and feelings.

NCT07032428 — Efficacy of kTMP, a Novel Non-invasive Brain Stimulation Method, for the Treatment of Anhedonia

StatusNot yet recruiting
PhaseN/A
SponsorMagnetic Tides
Enrollment104
Study TypeINTERVENTIONAL
ConditionsAnhedonia; Major Depressive Disorder (MDD)
Interventions;

The goal of this proposal is to provide a first assessment of the efficacy of our innovative non-invasive brain stimulation system, kTMP, in the treatment of anhedonia in MDD.

NCT07685964 — Pregnenolone for Cannabis Use Disorder and Depression

StatusNot yet recruiting
PhasePhase 1 / Phase 2
SponsorUniversity of Texas Southwestern Medical Center
Enrollment20
Study TypeINTERVENTIONAL
ConditionsCannabis Use Disorder; Major Depressive Disorder (MDD)
Interventions

This is UG3 phase of a multi-site, milestone-driven UG3/UH3 research program evaluating pregnenolone for individuals with co-occurring cannabis use disorder (CUD) and major depressive disorder (MDD). Pregnenolone is a neurosteroid that modulates cannabinoid receptor signaling and may reduce cannabis-related effects while also improving mood-related symptoms.

The primary objective of the UG3 ph…

Enrolling by Invitation

NCT07685925 — Intern Health Study 2026

StatusEnrolling by invitation
PhaseN/A
SponsorUniversity of Michigan
Enrollment1000
Study TypeINTERVENTIONAL
ConditionsDepression / Major Depressive Disorder; Mood; Sleep; Physical Activity
Interventions

The aim of this study is to evaluate the efficacy of using a reinforcement learning algorithm to determine the optimal content of a mobile health intervention (message delivered via smartphone) for improving the mood, physical activity, and sleep of medical interns.

NCT07149428 — Longitudinal Deep Phenotyping of Central Mechanisms in Dysosmia: A Pilot Study Using Electrobulbogram (EBG), Functional MRI (fMRI), and Diffusion-Weighted Imaging (DWI)

StatusEnrolling by invitation
PhaseN/A
SponsorNational Institute on Deafness and Other Communication Disorders (NIDCD)
Enrollment80
Study TypeOBSERVATIONAL
ConditionsRespiratory Tract Infection; Smell Disorder; Influenza; Rhinosinusitis; COVID-19

Background:

Loss of the sense of smell can seriously affect a person’s quality of life. The ability to smell can be damaged by many factors, including illnesses, injuries, and exposure to toxic chemicals. The effects can vary, including complete loss of smell, partial loss, and parosomia, which is when things smell differently than they should.

Objective:

To study how brain function changes …

Completed Trials

StatusCompleted
PhaseN/A
SponsorNational Institute of Mental Health (NIMH)
Enrollment1158
Study TypeOBSERVATIONAL
ConditionsMood Disorder

The purpose of this study is to investigate mood and behavior changes in the time period surrounding and including menopause. This is an observational study; volunteers who participate will not receive any new or experimental therapies.

Controversy exists regarding the relationship between estrogen and progesterone (gonadal steroid) changes and midlife-onset depression. This study will examine…

NCT00060775 — The Psychobiology of Childhood Temperament

StatusCompleted
PhaseN/A
SponsorNational Institute of Mental Health (NIMH)
Enrollment550
Study TypeOBSERVATIONAL
ConditionsDevelopmental Psychology

The purpose of this study is to use brain imaging technology to examine brain changes that occur in children when they are exposed to various kinds of emotional tasks and to determine if these changes are related to the child’s temperament.

Studies suggest that the risk for developing mood and anxiety disorders in preschool children may be linked to differences in temperament. The relationship…

NCT04903522 — Can the Affects Conveyed by Baroque Music Reduce Anxiety in Patients With Major Depressive Disorder ?

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment18
Study TypeINTERVENTIONAL
ConditionsMajor Depressive Disorder
Interventions

Major depressive disorder, or characterized depressive episode, is a common illness that limits psychosocial functioning and impairs quality of life. The initial goal of treatment for a major depressive episode is complete remission of depressive symptoms. The most commonly used treatments are antidepressants, psychotherapy or a combination of medication and psychotherapy.

Music therapy can be…

NCT04502758 — Sequential Bilateral Accelerated Theta Burst Stimulation in Adolescents With Suicidal Ideation

StatusCompleted
PhaseN/A
SponsorMayo Clinic
Enrollment58
Study TypeINTERVENTIONAL
ConditionsSuicidal Ideation; Major Depressive Disorder
Interventions;

The purpose of this study is to gather information regarding the use of a new type of transcranial magnetic stimulation (TMS) called theta burst stimulation (TBS) for suicidal ideation in adolescents with Major Depressive Disorder (MDD). The investigators hope to learn if this TMS treatment improves suicidal ideation over 10 days and clinical outcomes over 1 year of follow-up.

NCT07690709 — Eye-tracking Training for Older Adults

StatusCompleted
PhaseN/A
SponsorChinese University of Hong Kong
Enrollment78
Study TypeINTERVENTIONAL
ConditionsSubjective Memory Complaints; Anxiety
Interventions

The goal of this clinical trial is to learn if a computerized eye-tracking training program can improve mental health and thinking skills in older adults. The main questions it aims to answer are whether eye-tracking training can lower depressive and anxiety symptoms in older adults, and whether it can improve their ability to control impulses and pay attention.

Researchers will compare older …

NCT07683637 — Effect of Auricular Vagus Nerve Stimulation on Pain and Symptoms in Primary Dysmenorrhea

StatusCompleted
PhaseN/A
SponsorIstanbul Gelisim University
Enrollment40
Study TypeINTERVENTIONAL
ConditionsPrimary Dysmenorrhea (PD); Primary Dysmenorrhea
Interventions;

This study aims to investigate the effects of transcutaneous auricular vagus nerve stimulation (taVNS) on menstrual pain, pain threshold, depression, anxiety, menstrual symptoms, premenstrual syndrome, and functional and emotional impact of dysmenorrhea in young adult women with primary dysmenorrhea.

NCT05680727 — Individualized Functional Connectivity Targeting in aiTBS for Depression

StatusCompleted
PhasePhase 2
SponsorBrigham and Women’s Hospital
Enrollment40
Study TypeINTERVENTIONAL
ConditionsDepressive Disorder, Major; Depression; Mood Disorders; Mental Disorder; Psychiatric Disorder
Interventions

The goal of this clinical trial is to estimate the importance of neuroimaging in accelerated intermittent theta burst stimulation (aiTBS) for depression. Participants will receive aiTBS treatment, but they will not know if their treatment spot was found with neuroimaging or head measurements.

NCT06058013 — Study to Assess the Effects of Oral NMRA-335140 Versus Placebo in Participants With Major Depressive Disorder

StatusCompleted
PhasePhase 3
SponsorNeumora Therapeutics, Inc.
Enrollment430
Study TypeINTERVENTIONAL
ConditionsMajor Depressive Disorder
Interventions;

This is a randomized, double-blind, placebo-controlled, multicenter study to evaluate the effects of NMRA-335140 (formerly BTRX-335140) on symptoms of depression in participants with Major Depressive Disorder (MDD). The study design consists of a Screening Period (up to 28 days), and a 6-week Treatment Period (during which participants will receive either NMRA-335140 or placebo). At the complet…

NCT06832462 — A Prospective and Experimental Study on the Effect of One-Day of Acceptance and Commitment Therapy (ACT) on Psychological Flexibility, Psychological Capital, Anxiety and Depression Among Undergraduate Students.

StatusCompleted
PhaseN/A
SponsorUniversiti Teknologi Malaysia
Enrollment61
Study TypeINTERVENTIONAL
ConditionsAnxiety; Depression
Interventions

The goal of this study is to examine the effect of a one-day ACT intervention on psychological flexibility and psychological capital among undergraduate students at UTM who have anxiety and depression. Undergraduate students who scored moderate or above on anxiety and depression questionnaires during screening and volunteered to participate will be invited to a one-day ACT intervention. The par…

NCT06133309 — Phenomenological Explorations of the Esketamine-Induced Transient Dissociative State

StatusCompleted
PhaseN/A
SponsorCentre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Enrollment15
Study TypeINTERVENTIONAL
ConditionsDepressive Disorder
Interventions

Ketamine is an anaesthetic used in low doses to treat depressive disorders. A related molecule, Esketamine, has recently been launched on the market for the treatment of resistant depression. One of the side effects of ketamine, like Esketamine, is induction of transient dissociative state. Dissociation has been described as disruption in continuity of conscious thought and emotion, cognitive p…

NCT05927987 — Feasibility and Acceptability of Problem Management Plus (PM+) for Prisoners in the Netherlands - a Pilot RCT

StatusCompleted
PhaseN/A
SponsorVU University of Amsterdam
Enrollment56
Study TypeINTERVENTIONAL
ConditionsAnxiety Disorders; Psychological Distress; Depressive Disorder
Interventions

The goal of this pilot randomised controlled trial is to evaluate the feasibility and acceptability of the - specifically to the prison context adapted - World Health Organization’s Problem Management Plus (PM+) intervention for individuals detained in Dutch remand prisons. The main question[s] it aims to answer are:

  • To what extent is the contextually adapted PM+ intervention feasible and …

NCT07691021 — Narrative Therapy for Anxiety and Depression in Palestinian Refugee Adolescents

StatusCompleted
PhaseN/A
SponsorNablus University for Vocational and Technical Education
Enrollment120
Study TypeINTERVENTIONAL
ConditionsAnxiety; Depression - Major Depressive Disorder
Interventions

This study evaluated whether a culturally adapted 10-week narrative therapy program could reduce anxiety and depression symptoms among middle school students living in refugee camps in Northern Palestine. Adolescents aged 12-15 years from UNRWA-operated schools with moderate-to-severe anxiety and depression symptoms participated. The study used a quasi-experimental design with 120 students assi…

NCT06792136 — A Study of ONO-1110 in Patients With Major Depressive Disorder

StatusCompleted
PhasePhase 2
SponsorOno Pharmaceutical Co., Ltd.
Enrollment103
Study TypeINTERVENTIONAL
ConditionsMajor Depressive Disorder (MDD
Interventions;

To Evaluate the Efficacy and Safety of ONO-1110 in Patients with Major Depressive Disorder

NCT06979154 — Pilot Study of Personalized Aperiodic Transcranial Alternating Current Stimulation in Antenatal Depression (PandA-tACS)

StatusCompleted
PhaseN/A
SponsorUniversity of North Carolina, Chapel Hill
Enrollment6
Study TypeINTERVENTIONAL
ConditionsAntenatal Depression; Major Depressive Disorder; Major Depressive Disorder in Pregnancy; Healthy Controls
Interventions

The purpose of this study is to develop the safety, feasibility, and tolerability of a personalized transcranial alternating current stimulation (tACS) approach in antenatal depression.

NCT07364825 — Acute Psychiatric Care at Home for Lower-risk Patients With Acute Psychiatric Illness Who Require Inpatient Care

StatusCompleted
PhaseN/A
SponsorBrigham and Women’s Hospital
Enrollment41
Study TypeINTERVENTIONAL
ConditionsPsychosis; Anxiety; Depression; Behavioral and Psychiatric Symptoms of Dementia
Interventions

The goal of this pilot randomized controlled trial is to learn if adult patients with acute psychiatric conditions can receive hospital-level care at home. The main question it aims to answer is:

1. Estimate the eligibility rate for BHH among screened patients. What percentage of eligible patients agree to enroll in behavioral health home hospital (intervention)?

NCT07396779 — Cognitive Task-Based Walking Effects on Cognition, Mood, Sleep, and Quality of Life in Older Adults With Brain Fog

StatusCompleted
PhaseN/A
SponsorMedipol University
Enrollment90
Study TypeINTERVENTIONAL
ConditionsBrain Fog; Cognitive Impairment; Geriatric Population
Interventions;

This randomized controlled trial aims to investigate the effects of cognitive task-based walking exercise on cognitive function, depressive symptoms, sleep quality, and quality of life in older adults experiencing brain fog. Eligible participants will be randomly assigned to either a cognitive task-based walking exercise group or a walking-only exercise group. The intervention will be conducted…