Search Clinical Trials
Before medications are approved by the U.S. Food and Drug Administration (FDA) or before certain therapy methods are widely accepted as effective, they are tested on people who volunteer to participate in a clinical trial.
Organizations across the country are looking for people like you to take part in their research studies. The list of studies below have been selected from ClinicalTrials.gov based on their inclusion of one or more of the following terms: anxiety disorders, depression, OCD, PTSD, and bipolar disorder.
The Anxiety and Depression Association of America (ADAA) is supportive of research that is conducted through clinical trials. Participating in research can potentially help change the mental health outcomes for you and others who suffer anxiety, depression, and related disorders. You may learn about new interventions/treatments that are being considered.
Read this ADAA blog about things to know and questions to ask before committing to a clinical trial.
This website page is brought to you in partnership with ResearchMatch.
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Postpartum Care in the NICU (PeliCaN) Transitions
University of Pennsylvania
Stress Disorders, Post-Traumatic
Premature Birth
Postpartum Depression
Postpartum Anxiety
This is a randomized controlled trial of a dyad-centered, doula support and healthcare
coordination model of care in a large urban neonatal intensive care unit (NICU), which
serves a high-risk, low-income, majority Black population. In addition to doula support
and coordination of care in the NICU,1 expand
This is a randomized controlled trial of a dyad-centered, doula support and healthcare coordination model of care in a large urban neonatal intensive care unit (NICU), which serves a high-risk, low-income, majority Black population. In addition to doula support and coordination of care in the NICU, there will be a warm handoff to a community doula to continue the support once infants leave the Hospital of the University of Pennsylvania (HUP) NICU. Type: Interventional Start Date: Sep 2024 |
Massage for GAD: Neuroimaging and Clinical Correlates of Response
University of Utah
Generalized Anxiety Disorder
This clinical trial will compare the effects of Swedish massage or light touch therapy on
brain activity and symptoms of anxiety.
This is a randomized research study and subjects will be randomized into one of two study
touch intervention groups, and will have an equal chance of being placed in on1 expand
This clinical trial will compare the effects of Swedish massage or light touch therapy on brain activity and symptoms of anxiety. This is a randomized research study and subjects will be randomized into one of two study touch intervention groups, and will have an equal chance of being placed in one of the groups: 1. Swedish massage therapy twice per week for 6 weeks. 2. Light touch therapy twice per week for 6 weeks. The Primary Objective is to identify brain networks activated by touch interventions using fMRI brain imaging in subjects with generalized anxiety disorder. Subjects will undergo two fMRI scanning sessions (one before and one after) twice per week for 6 weeks of touch intervention. Subjects will also be asked to complete questionnaires on anxiety, stress and depression. Type: Interventional Start Date: May 2024 |
Tele-PROTECT Therapy: Effectiveness, Empowerment, and Implementation
Weill Medical College of Cornell University
Depression
Elder Abuse
The purpose of this randomized trial is to conduct a fully powered effectiveness trial of
video-delivered PROTECT (Tele-PROTECT) compared to a video-delivered depression education
(DepEd) control condition to be delivered to 140 English- and Spanish-speaking NYC elder
abuse victims. Investigators h1 expand
The purpose of this randomized trial is to conduct a fully powered effectiveness trial of video-delivered PROTECT (Tele-PROTECT) compared to a video-delivered depression education (DepEd) control condition to be delivered to 140 English- and Spanish-speaking NYC elder abuse victims. Investigators hypothesize three main aims: 1. Effectiveness Aim: Tele-PROTECT participants will have significantly greater and clinically meaningful reductions in depression when compared to the DepEd control; 2. Abuse Impact Aim: Tele-PROTECT participants will demonstrate greater safety related empowerment compared to DepEd control, which can help participants take steps to reduce risk; 3. Implementation Aim: Stakeholders' views of the factors impacting the implementation of Tele-PROTECT based on characteristics of the intervention, agency setting, and population served will contribute to a national dissemination of Tele-PROTECT Participants will - Receive 9 weeks of tele health psychotherapy delivered by a Master's level mental health clinician from the Weill Cornell Medicine research team. Participants will be assigned to "Tele-PROTECT" or "DepEd" psychotherapy randomly. - Participate in one baseline assessment and four follow-up assessments at weeks 3, 6, 9, and 12 administered by a trained member of the research team. Type: Interventional Start Date: Sep 2023 |
Self-Management Interventions After an ICD Shock
University of Washington
Implantable Defibrillator User
Stress Reaction
Ptsd
Stress Management
Social Cognitive Theory
This study, "Biobehavioral Intervention to Reduce PTSD Symptoms After an ICD Shock,"
addresses a critical need in cardiology care by describing the feasibility and
acceptability of a timely, highly promising, electronically-delivered intervention for
patients who have recently received an ICD deliv1 expand
This study, "Biobehavioral Intervention to Reduce PTSD Symptoms After an ICD Shock," addresses a critical need in cardiology care by describing the feasibility and acceptability of a timely, highly promising, electronically-delivered intervention for patients who have recently received an ICD delivered shock. The study intervention and outcomes are designed to reduce anxiety, enhance return to activities of daily living (ADLs), and prevent the development of severe distress and post-traumatic stress disorder (PTSD), and ultimately promote quality of life. The study is a two-arm, embedded mixed methods, randomized trial (N=60, 30/group). The purpose is to determine feasibility and potential effects of a self-management intervention (SPSM) plus usual care (UC) compared to UC alone, delivered during the critical 1 month period after an ICD shock when distress is high. The intervention will be delivered over 1 month following an ICD shock; a 6-month follow-up will be used to assess the sustainability of intervention effects and determine if the incidence of PTSD is reduced. SPSM includes: 1) training in heart rate (HR) self-monitoring; and 2) individualized learning through 4 self-paced, web-based modules. The study interventions are delivered at a crucial time, closely after an ICD shock when stress is high, but PTSD has not yet developed. The specific aims are to: 1) examine the effects of the SPSM intervention plus UC vs. UC alone on the primary outcome of ICD shock anxiety at 1 and 6 months post-shock event, 2) describe the impact of SPSM plus UC compared to UC alone on the secondary outcomes of total daily physical activity, depression, PTSD symptoms, QOL, salivary cortisol levels, and self-efficacy and outcome expectations at 1 and 6 months post-shock event, and 3) assess feasibility, acceptability, and safety of the SPSM intervention, SDOH will be used to describe differential responses to the SPSM intervention. This study fills a significant gap in the care of patients with an ICD, through the systematic testing of a brief, novel and cost-effective intervention that provides the knowledge and skills to improve quality of life. Study findings will be used to design future larger RCTs to test intervention effectiveness for more diverse samples and settings. Type: Interventional Start Date: Oct 2024 |
Post-Hospital Intervention for Veterans With Comorbid Bipolar and Substance Use Disorders
VA Office of Research and Development
Bipolar Disorder
Substance Use Disorders
This trial aims to evaluate the effectiveness of a novel intervention for Veterans with
co-occurring bipolar and substance use disorders following a psychiatric hospitalization.
Half of the participants will receive a specialized psychosocial intervention program,
while the other half will receive1 expand
This trial aims to evaluate the effectiveness of a novel intervention for Veterans with co-occurring bipolar and substance use disorders following a psychiatric hospitalization. Half of the participants will receive a specialized psychosocial intervention program, while the other half will receive an enhanced safety monitoring program, both provided in addition to their routine care. Type: Interventional Start Date: Nov 2020 |
Neurobiological Mechanisms of Aging and Stress on Prospective Navigation
Georgia Institute of Technology
Aging
Anxiety
Memory Impairment
Two hallmarks of both healthy aging and age-related disease are 1) memory and
navigational deficits, particularly in orienting towards goal locations and planning how
to navigate to them, and 2) increased susceptibility to stress and altered regulation of
the stress response. However, there are mar1 expand
Two hallmarks of both healthy aging and age-related disease are 1) memory and navigational deficits, particularly in orienting towards goal locations and planning how to navigate to them, and 2) increased susceptibility to stress and altered regulation of the stress response. However, there are marked individual differences in these age-related changes. The investigators' proposal will help characterize factors that contribute to this variability. Participants will be pseudorandomly assigned to stress-manipulated or control groups. The investigators will give both groups a novel immersive navigation task, validated by the PI in healthy young adults. This paradigm gives participants the opportunity to either (a) flexibly draw on spatial memory in order to plan efficient routes to goal locations, or (b) fall back on inefficient, but cognitively less-demanding, stimulus-response associations (i.e., habits). Using neuroimaging and behavioral measures, the investigators' protocol will test whether experimentally-induced stress leads individuals to bring fewer details about future locations to mind when route planning, and whether such restricted prospective thought ultimately biases participants towards relatively inflexible, habitual actions. Type: Interventional Start Date: Sep 2019 |
Studying the Health of Asians to Advance Knowledge, Treatments, and Interventions for Depression
University of Texas Southwestern Medical Center
Depression
Treatment Resistant Depression
Mood Disorders
Bipolar Disorder
Mental Disorders
SHAKTI (from the Sanskrit word for "power") is a 5-year natural history, longitudinal,
prospective study of a cohort of 6,000 participants that will help uncover the
socio-demographic, lifestyle, clinical, psychological, and neurobiological factors that
contribute to antidepressant treatment respon1 expand
SHAKTI (from the Sanskrit word for "power") is a 5-year natural history, longitudinal, prospective study of a cohort of 6,000 participants that will help uncover the socio-demographic, lifestyle, clinical, psychological, and neurobiological factors that contribute to antidepressant treatment response (remission, recurrence, relapse and individual outcomes in depressive disorders) and resilience. As this is an exploratory study, we will assess a comprehensive panel of carefully selected participant specific parameters - socio-demographic (age, sex, gender, race, ethnicity, economic); life habits (physical activity, substance use); clinical (medical history, anxious depression, early life trauma), biological (biomarkers in blood, saliva, urine, stool), behavioral (cognitive, emotional), neurophysiological (EEG), and neuroimaging (magnetic resonance imaging; MRI) with the goal of developing the most robust predictive models of depression treatment response and of outcomes. Type: Observational Start Date: Mar 2024 |
Self-Adjusted Nitrous Oxide: A Feasibility Study in the Setting of Vasectomy
Beth Israel Deaconess Medical Center
Procedural Pain
Pain Catastrophizing
Procedural Anxiety
This study is being done to see if nitrous oxide during vasectomy decreases pain and
anxiety, and also assess whether patients have better satisfaction when they control
their own level of nitrous oxide during the procedure. If we find that patients
experience less pain or anxiety with nitrous oxid1 expand
This study is being done to see if nitrous oxide during vasectomy decreases pain and anxiety, and also assess whether patients have better satisfaction when they control their own level of nitrous oxide during the procedure. If we find that patients experience less pain or anxiety with nitrous oxide, it could be suggested that self-adjusted nitrous oxide (SANO) may be a useful tool for improving experience of care during vasectomy. Type: Interventional Start Date: May 2023 |
Transforming Adolescent Mental Health Through Accessible, Scalable, Technology-supported Small-grou1
University of Oregon
Anxiety Depression
Suicidal Ideation
Adolescence is a developmental period of significant risk for anxiety, depressive
symptoms, and suicidality, and the investigators propose to target key peer-based risk
and protective factors using Cooperative Learning (CL). CL is a small-group instructional
approach that can enhance peer relations1 expand
Adolescence is a developmental period of significant risk for anxiety, depressive symptoms, and suicidality, and the investigators propose to target key peer-based risk and protective factors using Cooperative Learning (CL). CL is a small-group instructional approach that can enhance peer relations and reduce peer-related risks, as well as promote academic engagement and achievement and reduce racial disparities. CL will be delivered with the aid of technology that automates the design and delivery of CL lessons, promoting rapid implementation, scalability, high fidelity, accessibility, and sustainability. Type: Interventional Start Date: Sep 2023 |
ENCALM: a Study of ENX-102 As a Monotherapy Treatment in Patients with Generalized Anxiety Disorder
Engrail Therapeutics INC
Generalized Anxiety Disorder
The ENCALM trial is designed to evaluate the efficacy and safety of ENX-102 in patients
diagnosed with generalized anxiety disorder (GAD) expand
The ENCALM trial is designed to evaluate the efficacy and safety of ENX-102 in patients diagnosed with generalized anxiety disorder (GAD) Type: Interventional Start Date: Jul 2023 |
Technology-Assisted Implementation of a Mobile Health Program for Serious Mental Illness
University of Washington
Schizophrenia
Bipolar Disorder
Major Depressive Disorder
Schizo Affective Disorder
The goal of this clinical trial is to learn about how a digital training platform can
enhance implementation and effectiveness of a validated mHealth system, called FOCUS, in
people with serious mental illness. The main question this research aims to answer is
whether patients obtain similar outcom1 expand
The goal of this clinical trial is to learn about how a digital training platform can enhance implementation and effectiveness of a validated mHealth system, called FOCUS, in people with serious mental illness. The main question this research aims to answer is whether patients obtain similar outcomes to previous FOCUS studies when using FOCUS with clinicians trained on a newly developed digital training platform. Participants will be asked to use the FOCUS smartphone application and receive mobile health coaching from clinicians who have been trained using the digital training platform. Type: Interventional Start Date: Aug 2023 |
Academic-Community EPINET (AC-EPINET)
Indiana University
Schizophrenia
Schizoaffective Disorder
Schizophreniform Disorders
Major Depression with Psychotic Features
Bipolar Disorder with Psychotic Features
The investigators propose to examine the effects of CSC services delivered via TH
(CSC-TH) versus the standard clinic-based CSC model (CSC-SD) on engagement and outcomes
in a 12-month, randomized trial. expand
The investigators propose to examine the effects of CSC services delivered via TH (CSC-TH) versus the standard clinic-based CSC model (CSC-SD) on engagement and outcomes in a 12-month, randomized trial. Type: Interventional Start Date: Mar 2022 |
Determining Optimal Treatment Sequences in Anxious Depression (DOTS-AD)
University of Cincinnati
Anxious Depression
Depression
Acute, double-blind, adaptively randomized treatment with duloxetine or escitalopram,
followed by double-blind, randomized adjunctive treatment with clonazepam or pregabalin
for persistent symptoms. expand
Acute, double-blind, adaptively randomized treatment with duloxetine or escitalopram, followed by double-blind, randomized adjunctive treatment with clonazepam or pregabalin for persistent symptoms. Type: Interventional Start Date: Mar 2020 |
rTMS to Target Neural Connectivity and Rumination in Treatment-Resistant Depression
Indiana University
Depression, Treatment Resistant
The goal of this clinical trial is to learn if Transcranial Magnetic Stimulation (TMS) to
part of the brain called the ventromedial prefrontal cortex (VMPFC) can treat a symptom
called rumination in adults with major depression that has not responded to at least one
medication trial. The main quest1 expand
The goal of this clinical trial is to learn if Transcranial Magnetic Stimulation (TMS) to part of the brain called the ventromedial prefrontal cortex (VMPFC) can treat a symptom called rumination in adults with major depression that has not responded to at least one medication trial. The main question it aims to answer are: Does TMS to the VMPFC change brain activity on functional magnetic resonance imaging (fMRI) during a negative self-referential processing task in adults with depression? Does TMS to the VMPFC affect rumination in adults with depression? Researchers will compare brain scans and rumination scores before, during, and immediately after TMS. Participants will: Undergo three functional MRI scans Undergo a course of 20 TMS treatments Respond to clinical questionnaires and complete a computer behavioral task Type: Interventional Start Date: Jan 2024 |
Reducing Mental Health Disparities Among Latinxs With a Telenovela Intervention
University of Nevada, Reno
Anxiety Disorders
The primary aim of our study is to determine the effectiveness of an transdiagnostic
telenovela video intervention in reducing anxiety and depressive symptoms using a
pre/post-test design with Spanish-speaking Latinxs. expand
The primary aim of our study is to determine the effectiveness of an transdiagnostic telenovela video intervention in reducing anxiety and depressive symptoms using a pre/post-test design with Spanish-speaking Latinxs. Type: Interventional Start Date: Jul 2024 |
Music-Based Interventions, Aging, Alzheimer's Disease
University of Southern California
Speech Perception
Anxiety
Social Behavior
Using a randomized controlled trial design, the investigators will examine the effects of
music engagement through choir training on the hearing, communication, and psychosocial
well-being of older adults, particularly those at heightened risk of developing dementia. expand
Using a randomized controlled trial design, the investigators will examine the effects of music engagement through choir training on the hearing, communication, and psychosocial well-being of older adults, particularly those at heightened risk of developing dementia. Type: Interventional Start Date: Oct 2024 |
Psychotherapy Effects on Reward Processing in PTSD
University of Texas at Austin
Post Traumatic Stress Disorder
Diminished Pleasure
Anhedonia
PTSD
Chronic PTSD
The purpose of this study is to identify how trauma-focused psychotherapy changes the
function of brain circuitry in posttraumatic stress disorder (PTSD) and how this mediates
improvements in the diminished ability to experience positive emotions following a
traumatic or extremely stressful life ev1 expand
The purpose of this study is to identify how trauma-focused psychotherapy changes the function of brain circuitry in posttraumatic stress disorder (PTSD) and how this mediates improvements in the diminished ability to experience positive emotions following a traumatic or extremely stressful life event. In this instance, the investigators will be using cognitive processing therapy (CPT), a widely-utilized and evidence-based treatment for PTSD. Type: Interventional Start Date: Jun 2024 |
Cancer Pain Management Using a Web-based Intervention
University of Texas at Austin
Cancer of Breast
Depressive Symptoms
Cancer Pain
This study is funded by the HEAL Initiative (https://heal.nih.gov/). Based on Preliminary
Studies (PSs), the research team developed and pilot-tested an evidence-based Web
App-based information and coaching/support program for cancer pain management (CAPA) that
was culturally tailored to Asian Amer1 expand
This study is funded by the HEAL Initiative (https://heal.nih.gov/). Based on Preliminary Studies (PSs), the research team developed and pilot-tested an evidence-based Web App-based information and coaching/support program for cancer pain management (CAPA) that was culturally tailored to Asian American breast cancer survivors using multiple unique features. However, CAPA rarely considered depressive symptoms accompanying pain in its design or components, and PSs indicated the necessity of further individualization of the intervention components of CAPA due to diversities in the needs of ABD. The purpose of the proposed 2-phase study is to further develop CAPA with additional components for ABD and the individual optimization functionality (CAI) and to test the efficacy of CAI in improving cancer pain experience of ABD. The specific aims are to: a) develop and evaluate CAI through an expert review and a usability test (R61 phase); b) determine whether the intervention group (that uses CAI and usual care) will show significantly greater improvements than the active control group (that uses CAPA and usual care) in primary outcomes (cancer pain management and cancer pain experience including depressive symptoms) from baseline to post 1-month and post 3-months; c) identify theory-based variables (attitudes, self-efficacy, perceived barriers, and social influences) that mediate the intervention effects of CAI on the primary outcomes; and d) determine whether the effects of CAI on the primary outcomes are moderated by selected background, disease, genetic, and situational factors. This study is guided by the Bandura's Theory and the stress and coping framework by Lazarus and Folkman. The R61 phase includes: (a) the intervention development process, (b) a usability test among 15 ABD, 15 family members, and 15 community gatekeepers; and (c) an expert review among 10 experts in oncology. The R33 phase adopts a randomized repeated measures control group design among 300 ABD. Long-term goals are: (a) to extend and test CAI in various healthcare settings with diverse subgroups of ABD, (b) examine the costeffectiveness, sustainability, and scalability of CAI in the settings, and (c) translate CAI into health care for ABD. Type: Interventional Start Date: Feb 2024 |
PD, PK, and Safety of ALTO-203 in Patients With MDD
Alto Neuroscience
Major Depressive Disorder
Anhedonia
The goal of this clinical trial is to determine the pharmacodynamic effects of ALTO-203
in patients with MDD in a randomized, placebo-controlled, single-dose crossover treatment
period. Additionally, safety, tolerability, and PK will be assessed in a subsequent
randomized placebo-controlled multi-d1 expand
The goal of this clinical trial is to determine the pharmacodynamic effects of ALTO-203 in patients with MDD in a randomized, placebo-controlled, single-dose crossover treatment period. Additionally, safety, tolerability, and PK will be assessed in a subsequent randomized placebo-controlled multi-dose parallel-group treatment period of 28 days. Participants will complete subjective response questionnaires and perform cognitive tasks during the single-dose period, in which participants will receive ALTO-203 25 μg and 75 μg, as well as placebo. During the multiple-dose period, participants will receive either ALTO-203 25 μg, 75 μg , or placebo. Safety will be assessed over the single dose and 28-day multiple dose periods. Type: Interventional Start Date: Mar 2024 |
IN Midazolam vs IN Dexmedetomidine vs IN Ketamine During Minimal Procedures in Pediatric ED
University of Oklahoma
Laceration of Skin
Anxiety
Discharge Time
Pain in young children has been universally under-recognized due to their inability to
describe or localize pain. Improvements in pharmacological interventions are necessary to
optimize patient and family experience and allow for successful and efficient procedure
completion. This is the first stud1 expand
Pain in young children has been universally under-recognized due to their inability to describe or localize pain. Improvements in pharmacological interventions are necessary to optimize patient and family experience and allow for successful and efficient procedure completion. This is the first study that will compare three intranasal medications (Intranasal Midazolam, Dexmedetomidine, and Ketamine) to evaluate the length of stay after medication administration along with patient and provider satisfaction. The objective of this study is to demonstrate superior intranasal anxiolysis for pediatric laceration repairs with the shortest emergency department stay and highest patient and provider satisfaction. Based on previous studies and medication pharmacokinetics, we hypothesize that Intranasal Ketamine will have the shortest Emergency Department (ED) stay followed by Midazolam and then Dexmedetomidine with the longest stay; however, Dexmedetomidine will have the highest patient and provider satisfaction followed by Ketamine and then Midazolam. Type: Interventional Start Date: Nov 2023 |
Toward Understanding Drivers of Patient Engagement With Digital Mental Health Interventions - Part1
Brigham and Women's Hospital
Depression
Anxiety Disorders
This study is a clinical trial that evaluates what drives patient engagement and tests
the impact of two strategies-automated motivational push messaging and coach support-to
improve engagement with an evidence-based mobile app intervention for depression and/or
anxiety. expand
This study is a clinical trial that evaluates what drives patient engagement and tests the impact of two strategies-automated motivational push messaging and coach support-to improve engagement with an evidence-based mobile app intervention for depression and/or anxiety. Type: Interventional Start Date: Jun 2023 |
Development of a Transdiagnostic Intervention for Adolescents at Risk for Serious Mental Illness
Massachusetts General Hospital
Anxiety Disorders
Psychotic Disorders
Depressive Disorder
Psychosocial Functioning
This research study aims to develop a brief group-based treatment called Resilience
Training for Teens, then to test how well it protects high school students with mild
symptoms of depression, anxiety, or having unusual feelings from developing mental
illnesses. expand
This research study aims to develop a brief group-based treatment called Resilience Training for Teens, then to test how well it protects high school students with mild symptoms of depression, anxiety, or having unusual feelings from developing mental illnesses. Type: Interventional Start Date: Mar 2024 |
Antidepressant Effects of Nitrous Oxide
University of Chicago
Major Depressive Disorder
Treatment Resistant Depression
To evaluate the acute and sustained antidepressant effects of nitrous oxide in people
with major depressive disorder; and further evaluate these effects by identifying the
optimal dose and regimen to guide current practice, and to plan a future large pragmatic
trial. expand
To evaluate the acute and sustained antidepressant effects of nitrous oxide in people with major depressive disorder; and further evaluate these effects by identifying the optimal dose and regimen to guide current practice, and to plan a future large pragmatic trial. Type: Interventional Start Date: Jun 2021 |
Evaluating the Impact of Focused Muscle Contraction Therapy in U.S. Veterans
University of Illinois at Chicago
Chronic Pain
Acute Pain
Fatigue
Depression
This research study is being done to investigate if the GH Method exercise program
positively affects body composition, improves physical abilities and can improve the
overall sense of wellbeing (e.g. depression, PTSD, etc.) in U.S. Veterans. Subjects will
be asked to complete 94 total visits (four1 expand
This research study is being done to investigate if the GH Method exercise program positively affects body composition, improves physical abilities and can improve the overall sense of wellbeing (e.g. depression, PTSD, etc.) in U.S. Veterans. Subjects will be asked to complete 94 total visits (four (4) study testing visits and 90 exercise visits). Enrolled subjects will be tested for fitness, strength, and health risk factors at UIC 4 times and will complete 90 exercise training visits at the GH FITLab over the next 18 months. Subjects will also be asked to complete questionnaires about depression, post-traumatic stress symptoms and thoughts about harming oneself. Type: Interventional Start Date: Oct 2021 |
Behavioral Activation-Rehabilitation to Improve Depressive Symptoms & Physical Function After Acute1
Johns Hopkins University
Respiratory Insufficiency
Depression
Rehabilitation
Critical Care
More and more people are surviving after receiving life support for respiratory failure
in the intensive care unit, but these patients often experience problems with depression
and physical functioning that lead to reduced quality of life. There is a lack of
treatment for these patients, with past1 expand
More and more people are surviving after receiving life support for respiratory failure in the intensive care unit, but these patients often experience problems with depression and physical functioning that lead to reduced quality of life. There is a lack of treatment for these patients, with past research suggesting that treatment may be more successful if mental and physical health are addressed at the same time. This research evaluates whether a therapy delivered via telephone and home visits, combining treatment for depression and physical rehabilitation, is feasible and might help patients recover. Type: Interventional Start Date: Mar 2018 |
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