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Data sourced from ClinicalTrials.gov. Always consult a healthcare provider before enrolling.

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CompletedN/A

TODAY! A Mobile App Study

The aim of this study is to conduct a small randomized controlled trial (RCT) for a 10-week mobile phone intervention using principles of Cognitive Behavior Therapy to target general and minority stressors and treat anxiety and depression i

Chicago, Illinois, United StatesView details
CompletedN/A

Competence-feedback and Therapy Outcome

In a randomized controlled study design, n = 58 treatments of patients with depression were to be conducted under a feedback-condition, in which the therapist would receive feedback five times within 20 treatment sessions. The competence-fe

Mainz, GermanyView details
CompletedN/A

Effect of Music Therapy on Hospital Anxiety/Depression and Comfort Level

Aim: It has been determined that there are limited studies in our country where music is used as a nursing intervention and the effects of music therapy on the psychological symptoms and comfort levels of individuals with chronic diseases a

Merkez, Amasya, Turkey (Türkiye)View details
WithdrawnEARLY_Phase 1

Theophylline for Depression Study

Depression is very common and poses a huge disease burden. About 20% of the US population suffers from depression at least once in their lifetime.

Los Angeles, California, United StatesView details
CompletedN/A

Effects of Orally Administered Thymus Vulgaris Leaves on Memory, Anxiety, Depression, and Sleep Quality in University Students: A Randomized Controlled Trial

Thymus vulgaris could potentially serve as a safer alternative to stimulant drugs for enhancing memory among university students. Furthermore, Thymus vulgaris may offer additional benefits in terms of reducing anxiety, depression, and impro

Zarqa, JordanView details
CompletedPhase 4

Combination Treatment Study for Memory Impairment and Depression

Patients presenting with depression (DEP) and cognitive impairment (CI), represent a unique, understudied population that is difficult to diagnose, treat and estimate prognosis. Our pilot data, supported by the literature, suggest that many

New York, New York, United States+1 moreView details
CompletedN/A

Dyspnea and Psychosocial Effects of Hand Fan Application in COPD Patients

This randomized controlled trial aims to evaluate the effects of hand fan application on dyspnea, illness perception, anxiety, and depression in COPD patients. A total of 56 voluntary COPD patients (28 experimental, 28 control) will be recr

Ardahan, Ardahan, Turkey (Türkiye)View details
CompletedPhase 2

Open Label Extension Assessing the Tolerability of BCI-024 in Combination With BCI-049 in Patients With Major Depressive Disorder (MDD)

The objective of this study is to allow patients who have participated in the precursor study of BCI-024 in combination with BCI-049 versus placebo or BCI-024 alone (Protocol #CBM-IT-01) to receive 6 weeks of open-label treatment with an in

Garden Grove, California, United States+8 moreView details
CompletedN/A

Nurse Suicide: Physiologic Sleep Health Promotion Trial

The purpose of this study is to identify factors (sleep, psychiatric characteristics, stressful life events, and work environment characteristics) that potentiate or mitigate adverse effects of real-world stressors that predispose nurses to

Cortlandt Manor, New York, United StatesView details
UnknownN/A

Based-virtual Reality Diagnosis for Neuropsychiatric Diseases and Sleep/Wake Disorders

The objective of this research is to develop original virtual reality scenarios and/or new virtual reality equipments to evaluate or diagnose pathologies, such as attention deficit disorders or neuropsychiatric pathologies, addiction, anxie

Bordeaux, FranceView details
CompletedN/A

Implementation Trial of Evidence Based Practices for Mood Disorders

The objective of this Implementation Trial is to evaluate the implementation of evidence based practices for Bipolar Disorder and Treatment Resistant Depression in small rural Federally Qualified Health Centers. The evidence based practices

Eudora, Arkansas, United States+5 moreView details
By invitationN/A

Effectiveness of mHealth Post-discharge Intervention for Patients With Severe Mental Illness

The overall aim of this program of research is to improve the continuity of care for patients with serious mental illness (SMI) by supporting a safer and more efficient bridge from hospital to outpatient care using a mobile device-delivered

Providence, Rhode Island, United StatesView details
Not yet recruitingN/A

Telemedicine-mHealth Symptom Cluster Intervention for Advanced Cancer Patients: Finding Our Center Under Stress (FOCUS)

In response to the symptom needs experienced in advanced cancer, the investigators developed a brief, integrated CBT-ACT symptom management intervention, Finding Our Center Under Stress (FOCUS). Using FOCUS, participants learn skills to sel

Columbus, Ohio, United StatesView details
WithdrawnN/A

Late-life Depression and Cerebral Perfusion

The long-term goal is to determine if decreased blood flow to the brain (cerebral hypoperfusion) is predictive of antidepressant outcomes in late-life depression (LLD). Studies in younger adult report that successful antidepressant treatmen

Nashville, Tennessee, United StatesView details
CompletedPhase 1

Enhancing the Effects of Alcohol Treatment With L-Carnitine

The primary objective of this study is to evaluate the effects of L-carnitine, 2.97g daily on alcohol cue-elicited alcohol craving during a human laboratory paradigm after 4 weeks of daily dosing among participants ages 18-25 with alcohol u

Providence, Rhode Island, United StatesView details
CompletedN/A

Project Collabri for Treatment of Depression

The purpose of this study is to determine whether treatment of patients with depression according to the Collabri Model is more effective in reducing symptoms compared to treatment as usual (TAU)

Copenhagen, DenmarkView details
CompletedPhase 3

An Open-label Study of Lumateperone as Adjunctive Therapy in the Treatment of Patients With Major Depressive Disorder

This is a multicenter, open-label, fixed dose, 26 week study of patients with MDD. Eligible patients from the lead-in studies will enter the Open-label Safety Study at the Screening/Baseline Visit (Visit 1/Day 1), at which point patient eli

Phoenix, Arizona, United States+108 moreView details
CompletedPhase 3

Deprexil in Subjects With Signs and Symptoms of Depression

The purpose of the study is to assess the efficacy of DEPREXIL administration in combination with relaxation psychotherapy in the treatment of patients with signs and symptoms of depression. The duration of this double-blind placebo control

Havana, La Habana, CubaView details
UnknownN/A

ICBT for Mental Health Problems Related to the Climate Crisis

The study seeks to investigate the effects of a guided internet-based cognitive behavioral therapy (ICBT) programme on adult mental health problems related to the climate crisis. ICBT will be compared to a wait-list control group.

Linköping, Östergötland County, SwedenView details
CompletedN/A

Storytelling Video Intervention for Depressed Primary Care Patients - Pilot Trial

The overall aim of this program of research is to refine and test a newly developed storytelling video intervention (sTVi) for depressed primary care patients. The purpose of the proposed project is to establish the feasibility, acceptabili

Providence, Rhode Island, United StatesView details
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