Anxiety disorders are treatable. Most people are treated with talk therapy, medicine, or both. Common first medicines are selective serotonin reuptake inhibitors (SSRIs) and serotonin-norepinephrine reuptake inhibitors (SNRIs). Each card links to its source: a U.S. Food and Drug Administration (FDA) label or record, a National Institute of Mental Health (NIMH) page, or, for treatments still in clinical trials, the trial registry or company announcement.
Antidepressants and young people
Antidepressant labels carry an FDA boxed warning: in short-term studies, antidepressants increased suicidal thoughts and behaviors in children, teens, and young adults. Anyone starting a medicine or changing a dose should be watched closely, especially in the first few weeks. Never stop a medicine without talking to the prescriber.
All benzodiazepines carry an FDA boxed warning about abuse, misuse, addiction, physical dependence, and withdrawal reactions. Taking them with opioids or alcohol can slow breathing dangerously, and stopping suddenly can cause serious withdrawal, including seizures.
Started a medicine and still not feeling better?Antidepressants used for anxiety may take several weeks to start working, and there are next steps if the first one does not help.Source
Curious what people say online?A separate social media analysis counts how often people posting on Reddit said each anxiety medicine helped. It reflects self-selected online posts, not clinical evidence, and is not a recommendation.
Lexapro · a selective serotonin reuptake inhibitor (SSRI)
Generalized anxiety disorder (GAD) in adults and children 7 and older
An antidepressant from the SSRI group. SSRIs and similar antidepressants are commonly used to treat anxiety disorders.
Show details
What it is
An antidepressant from the SSRI group. SSRIs and similar antidepressants are commonly used to treat anxiety disorders.
FDA status / limitation
The Lexapro label covers generalized anxiety disorder in adults and in children 7 years and older.
Typical use
A daily tablet or liquid. Like other antidepressants used for anxiety, it may take several weeks to start working.
Safety flags
Side effects such as headaches, nausea, or trouble sleeping are usually not severe, especially when the dose starts low and rises slowly. Do not combine with monoamine oxidase inhibitors (MAOIs), and do not stop suddenly, because withdrawal symptoms can occur. Boxed warning: antidepressants increased suicidal thoughts and behaviors in children, teens, and young adults in short-term studies. Everyone starting one should be watched closely, especially in the first weeks and after dose changes.
Panic disorder · social anxiety disorder · GAD, in adults
An SSRI antidepressant with several anxiety uses on its label.
Show details
What it is
An SSRI antidepressant with several anxiety uses on its label.
FDA status / limitation
The Paxil label covers panic disorder, social anxiety disorder, and generalized anxiety disorder in adults, along with obsessive-compulsive disorder and post-traumatic stress disorder. The extended-release Paxil CR label covers panic disorder and social anxiety disorder.
Typical use
A daily tablet. Full effect can take several weeks.
Safety flags
Side effects such as headaches, nausea, or trouble sleeping are usually not severe, especially when the dose starts low and rises slowly. Do not combine with monoamine oxidase inhibitors (MAOIs), and do not stop suddenly, because withdrawal symptoms can occur. The National Institute for Health and Care Excellence (NICE) notes paroxetine is especially likely to cause a withdrawal syndrome. Boxed warning: antidepressants increased suicidal thoughts and behaviors in children, teens, and young adults in short-term studies. Everyone starting one should be watched closely, especially in the first weeks and after dose changes.
Panic disorder · social anxiety disorder, in adults
An SSRI antidepressant. NICE guidance suggests it as the first medicine to try for generalized anxiety disorder, a use that is not on the U.S. label.
Show details
What it is
An SSRI antidepressant. NICE guidance suggests it as the first medicine to try for generalized anxiety disorder, a use that is not on the U.S. label.
FDA status / limitation
The Zoloft label covers panic disorder and social anxiety disorder in adults, along with obsessive-compulsive disorder, post-traumatic stress disorder, and other conditions.
Typical use
A daily tablet or liquid. Full effect can take several weeks.
Safety flags
Side effects such as headaches, nausea, or trouble sleeping are usually not severe, especially when the dose starts low and rises slowly. Do not combine with monoamine oxidase inhibitors (MAOIs), and do not stop suddenly, because withdrawal symptoms can occur. Boxed warning: antidepressants increased suicidal thoughts and behaviors in children, teens, and young adults in short-term studies. Everyone starting one should be watched closely, especially in the first weeks and after dose changes.
Panic disorder, with or without agoraphobia, in adults
One of the most widely used SSRI antidepressants.
Show details
What it is
One of the most widely used SSRI antidepressants.
FDA status / limitation
The Prozac label covers panic disorder with or without agoraphobia, along with obsessive-compulsive disorder and other conditions.
Typical use
A daily capsule. Full effect can take several weeks.
Safety flags
Side effects such as headaches, nausea, or trouble sleeping are usually not severe, especially when the dose starts low and rises slowly. Do not combine with monoamine oxidase inhibitors (MAOIs), and do not stop suddenly, because withdrawal symptoms can occur. Boxed warning: antidepressants increased suicidal thoughts and behaviors in children, teens, and young adults in short-term studies. Everyone starting one should be watched closely, especially in the first weeks and after dose changes.
Effexor XR · a serotonin-norepinephrine reuptake inhibitor (SNRI)
GAD · social anxiety disorder · panic disorder, in adults
An antidepressant from the SNRI group, used alongside SSRIs for anxiety disorders.
Show details
What it is
An antidepressant from the SNRI group, used alongside SSRIs for anxiety disorders.
FDA status / limitation
The Effexor XR label covers generalized anxiety disorder, social anxiety disorder, and panic disorder in adults.
Typical use
A daily capsule. Full effect can take several weeks.
Safety flags
Side effects such as headaches, nausea, or trouble sleeping are usually not severe, especially when the dose starts low and rises slowly. Do not combine with monoamine oxidase inhibitors (MAOIs), and do not stop suddenly, because withdrawal symptoms can occur. NICE notes venlafaxine is especially likely to cause a withdrawal syndrome and is more dangerous in overdose. Boxed warning: antidepressants increased suicidal thoughts and behaviors in children, teens, and young adults in short-term studies. Everyone starting one should be watched closely, especially in the first weeks and after dose changes.
An SNRI antidepressant that is also used for some kinds of long-lasting pain.
Show details
What it is
An SNRI antidepressant that is also used for some kinds of long-lasting pain.
FDA status / limitation
The duloxetine label covers generalized anxiety disorder in adults and in children 7 years and older, along with several pain conditions.
Typical use
A daily capsule. Full effect can take several weeks.
Safety flags
Side effects such as headaches, nausea, or trouble sleeping are usually not severe, especially when the dose starts low and rises slowly. Do not combine with monoamine oxidase inhibitors (MAOIs), and do not stop suddenly, because withdrawal symptoms can occur. Boxed warning: antidepressants increased suicidal thoughts and behaviors in children, teens, and young adults in short-term studies. Everyone starting one should be watched closely, especially in the first weeks and after dose changes.
Anxiety disorders · short-term relief of anxiety symptoms
A different type of anti-anxiety medicine that NIMH says can be used to treat anxiety over longer periods.
Show details
What it is
A different type of anti-anxiety medicine that NIMH says can be used to treat anxiety over longer periods.
FDA status / limitation
The label covers the management of anxiety disorders and short-term relief of anxiety symptoms.
Typical use
Taken every day. It needs 3 to 4 weeks to reach full effect and does not work on an as-needed basis.
Safety flags
The most common side effects on the label are dizziness, drowsiness, nausea, headache, and nervousness. Do not take it with an MAOI or within 14 days of stopping one.
generic hydroxyzine hydrochloride · an antihistamine
Symptom relief of anxiety and tension
An antihistamine. MedlinePlus lists relieving anxiety and tension among its uses, along with itching from allergic skin reactions and sedation around surgery.
Show details
What it is
An antihistamine. MedlinePlus lists relieving anxiety and tension among its uses, along with itching from allergic skin reactions and sedation around surgery.
FDA status / limitation
The label covers symptom relief of anxiety and tension linked to psychoneurosis, and says its effectiveness for longer than 4 months has not been studied.
Typical use
Taken as directed by the prescriber. Ask how often to take it and for how long.
Safety flags
Can cause drowsiness and dry mouth, and adds to the effect of alcohol and other medicines that slow the brain. The label warns about a heart rhythm problem called QT prolongation and says not to use it in early pregnancy.
Short-term physical symptoms, such as performance anxiety
Heart and blood pressure medicines that can calm a racing heart, sweating, and trembling.
Show details
What it is
Heart and blood pressure medicines that can calm a racing heart, sweating, and trembling.
FDA status / limitation
Not approved for anxiety. The National Institute of Mental Health (NIMH) says providers may prescribe them off-label for short-term anxiety symptoms, and that they are commonly the medicine of choice for the performance anxiety type of social anxiety disorder.
Typical use
Taken as needed before a situation that sets off physical symptoms.
Safety flags
Generally not recommended for people with asthma or diabetes, because they may worsen both conditions.
alprazolam (Xanax), clonazepam (Klonopin), lorazepam (Ativan), diazepam (Valium), and others
Alprazolam: GAD and panic disorder · clonazepam: panic disorder · lorazepam and diazepam: anxiety disorders
Sedative anti-anxiety medicines that work quickly. Because tolerance and dependence can develop, providers may prescribe them only for brief periods.
Show details
What it is
Sedative anti-anxiety medicines that work quickly. Because tolerance and dependence can develop, providers may prescribe them only for brief periods.
FDA status / limitation
Each label lists its own anxiety uses, as shown above. The U.S. Food and Drug Administration (FDA) requires a boxed warning on all benzodiazepines about abuse, misuse, addiction, physical dependence, and withdrawal reactions. NICE advises against them for generalized anxiety disorder except briefly in a crisis, and against them for panic disorder.
Typical use
Usually short-term or as needed, at the lowest dose that works, with regular check-ins.
Safety flags
Physical dependence can develop after several days to weeks, even as prescribed. Stopping suddenly or cutting the dose too fast can cause withdrawal reactions, including seizures, so any taper should be slow and planned with the prescriber. Combining them with opioids, alcohol, or other sedating medicines can cause severe breathing problems and death.
GAD · panic disorder · social anxiety disorder · phobias
A therapy that helps people notice anxious or unhelpful automatic thoughts, question them, and change the behaviors that keep anxiety going. NIMH calls CBT the gold standard therapy for generalized anxiety disorder and social anxiety disorder.
Show details
What it is
A therapy that helps people notice anxious or unhelpful automatic thoughts, question them, and change the behaviors that keep anxiety going. NIMH calls CBT the gold standard therapy for generalized anxiety disorder and social anxiety disorder.
FDA status / limitation
There is no FDA approval process for psychotherapies. NIMH lists CBT as research-supported for each major anxiety disorder. NICE recommends individual CBT, usually 12 to 15 weekly one-hour sessions for generalized anxiety disorder, with applied relaxation as an alternative.
Typical use
One-on-one or in a group, in person or online. Group CBT can offer extra benefits for social anxiety.
Safety flags
Finding a therapist you trust matters. It is fine to ask about their training and approach before starting.
Panic disorder · social anxiety disorder · phobias
Facing feared situations, objects, or body sensations step by step in a supportive setting, from least to most frightening, until the fear fades. For panic, interoceptive exposure practices the body sensations of a panic attack.
Show details
What it is
Facing feared situations, objects, or body sensations step by step in a supportive setting, from least to most frightening, until the fear fades. For panic, interoceptive exposure practices the body sensations of a panic attack.
FDA status / limitation
NIMH describes exposure therapy as a CBT method for anxiety disorders. MedlinePlus lists exposure-based treatment among the talk therapies often tried first for specific phobias.
Typical use
Practiced with a therapist and between sessions. It may be combined with relaxation exercises.
Safety flags
It is meant to feel uncomfortable but manageable. Work at a pace agreed with the therapist.
A therapy that encourages accepting thoughts and feelings without judging them, and committing to meaningful activities. It uses mindfulness and goal setting.
Show details
What it is
A therapy that encourages accepting thoughts and feelings without judging them, and committing to meaningful activities. It uses mindfulness and goal setting.
FDA status / limitation
NIMH says a growing body of research shows it works for generalized anxiety disorder and social anxiety disorder.
Typical use
One-on-one or in a group, with a trained therapist.
A smartphone app that delivers CBT techniques for generalized anxiety disorder.
Show details
What it is
A smartphone app that delivers CBT techniques for generalized anxiety disorder.
FDA status / limitation
FDA cleared Daylight on August 30, 2024, as a prescription digital therapeutic to improve generalized anxiety disorder symptoms as an add-on to usual care in adults 22 and older. It was tested in a trial of 351 adults against online anxiety education.
Typical use
Available on the order of a licensed health care provider, who can follow progress through an online portal. It adds to care; it does not replace a clinician.
Safety flags
Not for emergencies. Contact a clinician or 988 if anxiety gets worse or thoughts of self-harm appear.
Symptoms of panic disorder · stress and anxiety symptoms in teens 13 to 17
A system that leads the user through guided, monitored breathing exercises.
Show details
What it is
A system that leads the user through guided, monitored breathing exercises.
FDA status / limitation
FDA cleared Freespira on August 23, 2018, as an add-on treatment for symptoms of panic disorder and post-traumatic stress disorder. A clearance on April 25, 2025, added teens 13 to 17 for symptoms of stress and anxiety.
Typical use
Prescription only, used under the direction of a health care professional together with other treatment.
Safety flags
An add-on, not a replacement for therapy or medicine.
A dissolving tablet (orally disintegrating tablet, or ODT) form of LSD, a psychedelic, tested as a single supervised dose.
Show details
What it is
A dissolving tablet (orally disintegrating tablet, or ODT) form of LSD, a psychedelic, tested as a single supervised dose.
Access boundary
Not FDA approved. Available only to people enrolled in a clinical trial. Not something to buy, order online, or try on your own.
Where it stands
Status as of September 2026: the company reported two positive Phase 3 trials in generalized anxiety disorder, Voyage (August 12, 2026) and Panorama (September 14, 2026). It plans to meet FDA in late 2026 and expects to file for approval in the first half of 2027 (company projection).
Typical use
Only given within clinical trials today. In Panorama, people were monitored for at least 8 hours on dosing day.
Safety flags
A psychedelic that causes temporary changes in perception and thinking, so trial doses are given under medical supervision. The company reports mostly mild to moderate side effects on the dosing day and no suicidality signal. Safety is still being studied.
A daily pill being tested against placebo over 8 weeks for generalized anxiety disorder.
Show details
What it is
A daily pill being tested against placebo over 8 weeks for generalized anxiety disorder.
Access boundary
Not FDA approved. Available only to people enrolled in a clinical trial. Not something to buy, order online, or try on your own.
Where it stands
Status as of October 2026 (trial registry): two Phase 3 trials, planning about 576 and 384 adults, began recruiting in mid-2026. Main results are estimated in late 2028.
Typical use
Only given within clinical trials today.
Safety flags
Safety for this use is still being studied. Ask the trial team about risks.
On-demand treatment of social anxiety disorder in adults 18 to 65
A capsule tested as a single dose, compared with placebo.
Show details
What it is
A capsule tested as a single dose, compared with placebo.
Access boundary
Not FDA approved. Available only to people enrolled in a clinical trial. Not something to buy, order online, or try on your own.
Where it stands
Status as of October 2026 (trial registry): a Phase 3 trial of about 500 adults has finished recruiting, with main results estimated in December 2026. No results have been posted yet.
Typical use
Only given within clinical trials today.
Safety flags
Safety is still being studied. Ask the trial team about risks.
JNJ-99245354 (Intra-Cellular Therapies, Johnson & Johnson)
Added to current treatment for GAD that has not responded well enough
A once-daily pill being tested as an add-on for adults whose generalized anxiety disorder has not improved enough with their current treatment.
Show details
What it is
A once-daily pill being tested as an add-on for adults whose generalized anxiety disorder has not improved enough with their current treatment.
Access boundary
Not FDA approved. Available only to people enrolled in a clinical trial. Not something to buy, order online, or try on your own.
Where it stands
Status as of October 2026 (trial registry): an add-on Phase 3 trial of about 705 adults is listed as not yet recruiting, and a long-term Phase 3 safety study is recruiting.
Typical use
Only given within clinical trials today.
Safety flags
Safety is still being studied. Ask the trial team about risks.
Medicine names, uses, and warnings come from FDA labels on DailyMed, FDA device records and safety pages, NIMH, MedlinePlus, and NICE guidance. Cards marked In clinical trials cite the trial registry or the company's own announcement, and company plans can change. Status was checked on October 8, 2026. Labels change; check the linked source for the latest.
Everyday habits
Things that can help alongside treatment
Healthy habits that NIMH and MedlinePlus describe. They can help alongside care; they are not a substitute for diagnosis or treatment.
Talk with a health care provider before starting any supplement or making big changes.
Caffeine and sleep
NIMH healthy habits
Cutting back on caffeine and getting enough sleep can reduce anxiety symptoms.
Researchers found these choices helped when paired with standard care such as psychotherapy and medicine.
MedlinePlus lists this among the self-care steps that can help. If you are prescribed a sedative, do not drink alcohol while taking it.
If substance use is part of the picture, see the Substance Abuse and Mental Health Services Administration (SAMHSA) National Helpline on the Resources page.
1,208 anxiety studies were recruiting on ClinicalTrials.gov as of October 8, 2026. Below are 50 of them, each with at least one site in the United States, picked to cover different anxiety disorders, age groups, and kinds of treatment: medicines, therapy, and devices.
Talk with your doctor before joining a trial
A listing here is not a recommendation. Studies test treatments that may not work or may have side effects, and each one has its own rules about who can join. Ask your doctor, or your child's doctor, whether a study fits, and keep taking current treatment unless your care team says otherwise. A research study is not emergency care: in a crisis, call or text 988.
Find a study near you
This opens ClinicalTrials.gov with recruiting anxiety studies already selected. Type your city or ZIP code in the Location box to see studies close to home.
ITI-1284 as an add-on in people with generalized anxiety disorder
Generalized anxiety
What is tested:
ITI-1284 10 mg, ITI-1284 20 mg
Who can join:
Any age · Generalized Anxiety Disorder
Where:
25 US sites in California, Florida, Texas and 8 more states · also Bulgaria, Czechia, Poland and 1 more country
Sponsor:
Intra-Cellular Therapies, Inc
Titles on ClinicalTrials.gov
Brief title: Study of ITI-1284 as an Adjunctive Treatment in Patients With Generalized Anxiety Disorder
Official title: A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of ITI-1284 as an Adjunctive Treatment in Patients With Generalized Anxiety Disorder Who Have an Inadequate Response to Generalized Anxiety Disorder Treatment
ITI-1284 on its own in people with generalized anxiety disorder
Generalized anxiety
What is tested:
ITI-1284 10 mg, ITI-1284 20 mg
Who can join:
Ages 18 and older · Generalized Anxiety Disorder
Where:
25 US sites in California, Florida, New York and 10 more states · also Bulgaria, Poland, Serbia and 1 more country
Sponsor:
Intra-Cellular Therapies, Inc
Titles on ClinicalTrials.gov
Brief title: Study of ITI-1284 as Monotherapy Treatment in Patients With Generalized Anxiety Disorder
Official title: A Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy, Safety, and Tolerability of ITI-1284 as Monotherapy Treatment in Patients With Generalized Anxiety Disorder Who Have Had Inadequate Response to Generalized Anxiety Disorder Treatment
Oral ABBV-932 added to antidepressant therapies in adults with generalized anxiety disorder
Generalized anxiety
What is tested:
ABBV-932, Antidepressant Therapy (ADT)
Who can join:
Ages 18 to 65 · Generalized Anxiety Disorder (GAD)
Where:
49 US sites in California, Florida, Texas and 19 more states · also Puerto Rico
Sponsor:
AbbVie
Titles on ClinicalTrials.gov
Brief title: Study to Assess Adverse Events and Change in Disease Activity When Oral ABBV-932 is Added to Antidepressant Therapies in Adult Participants With Generalized Anxiety Disorder
Official title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Fixed-Dose Study to Evaluate the Efficacy, Safety, and Tolerability of ABBV-932 as an Adjunct to Antidepressant Therapies in the Treatment of Subjects With Generalized Anxiety Disorder Who Have Had an Inadequate Response to Antidepressant Therapies
Fixed doses of SEP-363856 in adults with generalized anxiety disorder
Generalized anxiety
What is tested:
SEP-363856
Who can join:
Ages 18 and older · Generalized Anxiety Disorder
Where:
6 US sites in Florida, Arizona, Nevada and 2 more states
Sponsor:
Otsuka Pharmaceutical Development & Commercialization, Inc
Titles on ClinicalTrials.gov
Brief title: A Trial of the Efficacy and Safety of Fixed Doses of SEP-363856 in Adults With Generalized Anxiety Disorder
Official title: A Phase 3, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multicenter Trial to Compare the Efficacy and Safety of Fixed Doses of SEP-363856 to Placebo in the Treatment of Adults With Generalized Anxiety Disorder
A fixed dose of SEP-363856 in adults with generalized anxiety disorder
Generalized anxiety
What is tested:
SEP-363856
Who can join:
Ages 18 and older · Generalized Anxiety Disorder
Where:
5 US sites in California, Florida, New Jersey and 2 more states
Sponsor:
Otsuka Pharmaceutical Development & Commercialization, Inc
Titles on ClinicalTrials.gov
Brief title: A Trial of the Efficacy and Safety of a Fixed Dose of SEP-363856 in Adults With Generalized Anxiety Disorder
Official title: A Phase 3, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multicenter Trial to Compare the Efficacy and Safety of a Fixed Dose of SEP-363856 to Placebo in the Treatment of Adults With Generalized Anxiety Disorder
11 US sites in California, Florida, Massachusetts and 4 more states
Sponsor:
Newleos Therapeutics, Inc
Titles on ClinicalTrials.gov
Brief title: A Study of NTX-1472 in Social Anxiety Disorder
Official title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety, Tolerability, and Efficacy of NTX-1472, a V1a Receptor Antagonist, in Adults With Social Anxiety Disorder
A mechanistic study to assess a single dose of CYB003 in people with depression and anxiety
Anxiety in general or mixed
What is tested:
CYB003
Who can join:
Ages 21 to 65 · Depression, Anxiety
Where:
1 US site in Ohio
Sponsor:
Ohio State University
Titles on ClinicalTrials.gov
Brief title: A Mechanistic Study to Assess a Single Dose of CYB003 in Participants With Depression and Anxiety
Official title: A Randomized, Double-Blind, Placebo-Controlled Mechanistic Study to Assess a Single Oral Dose of CYB003 in Participants With Major Depressive Disorder (MDD) and Moderate to Severe Anxiety
RecruitingNo phase (therapy or device study)Therapy, behavioral, or digital
Screening and treatment for anxiety and depression (S.T.A.N.D.): Alacrity Center signature project
Anxiety in general or mixed
What is tested:
Self-Guided Online Prevention, Coach-Guided Online Cognitive Behavioral Therapy, Clinician-Delivered Psychological and Psychiatric Care
Who can join:
Ages 18 to 40 · Depression, Anxiety
Where:
1 US site in California
Sponsor:
University of California, Los Angeles
Titles on ClinicalTrials.gov
Brief title: S.T.A.N.D. Alacrity Center Signature Project
Official title: Screening and Treatment for Anxiety & Depression (S.T.A.N.D): Alacrity Center Signature Project on Triaging and Adapting to Level of Care
RecruitingNo phase (therapy or device study)Therapy, behavioral, or digital
Comparing transdiagnostic behavior therapy (TBT) to disorder-specific psychotherapy in veterans with social anxiety disorder
Social anxiety
What is tested:
Transdiagnostic Behavior Therapy, Cognitive Behavioral Therapy for Social Anxiety Disorder
Who can join:
Ages 18 to 80 · Social Anxiety Disorder
Where:
1 US site in South Carolina
Sponsor:
U.S. Department of Veterans Affairs (VA) Office of Research and Development
Titles on ClinicalTrials.gov
Brief title: Comparing TBT to Disorder-Specific Psychotherapy in Veterans With Social Anxiety Disorder
Official title: A Randomized Clinical Trial Comparing Transdiagnostic Behavior Therapy to Disorder-Specific Psychotherapy in the Recovery of Veterans With Social Anxiety Disorder and Comorbid PTSD Symptomatology
Abbreviations: PTSD means post-traumatic stress disorder
RecruitingNo phase (therapy or device study)Therapy, behavioral, or digital
Video game play to alleviate adolescent anxiety
Children and teens · Anxiety in general or mixed
What is tested:
Eco-Rescue, Bejelewed 3
Who can join:
Ages 11 to 15 · Anxiety, Anxiety Disorders and Symptoms
Where:
1 US site in Florida · also Israel, Switzerland
Sponsor:
School of Health Sciences Geneva
Titles on ClinicalTrials.gov
Brief title: Video Game Play to Alleviate Adolescent Anxiety
Official title: Evaluating the Effect of Gamified Cognitive Training and of Casual Videogame Play on Anxiety in Adolescents: Protocol for a Randomized Controlled Trial
RecruitingNo phase (therapy or device study)Therapy, behavioral, or digital
Personalized artificial intelligence (AI)-driven models in cognitive behavioral therapy for anxiety
Generalized anxiety
What is tested:
Explicit CBT SAR Personalization for 6 weeks, Implicit CBT SAR Personalization for 6 weeks, Control CBT SAR for 6 weeks
Who can join:
Ages 18 and older · Generalized Anxiety Disorder (GAD)
Where:
1 US site in California
Sponsor:
University of Southern California
Titles on ClinicalTrials.gov
Brief title: Personalized AI-Driven Models in Cognitive Behavioral Therapy for Anxiety
Official title: SCH: Personalized AI-Driven Models for Supporting User Engagement and Adherence in Health Interventions: Validation in Cognitive Behavioral Therapy for Anxiety
RecruitingNo phase (therapy or device study)Therapy, behavioral, or digital
Brain activity changes after cognitive behavioral therapy for anxiety in autistic youth from high-need communities
Children and teens · Anxiety in general or mixed
What is tested:
Facing Your Fears (FYF) Intervention: A CBT Focused Group Treatment for Autistic Youth with Anxiety
Who can join:
Ages 8 to 14 · Autism Spectrum Disorder, Anxiety
Where:
2 US sites in New Jersey, Pennsylvania
Sponsor:
Montclair State University
Titles on ClinicalTrials.gov
Brief title: Brain Activity Changes After Cognitive Behavioral Therapy for Anxiety in Autistic Youth From High-Need Communities
Official title: Electrophysiological Correlates of Anxiety-related Improvements Following Cognitive Behavioral Therapy for Autistic Youth in High-Need Communities
The impact of melatonin lotion on sleep and mental health
With another health condition · Anxiety in general or mixed
What is tested:
Melatonin lotion
Who can join:
Ages 18 to 21 · Sleep Problems, Depressive Disorder and Anxiety Disorders
Where:
1 US site in California
Sponsor:
University of Redlands
Titles on ClinicalTrials.gov
Brief title: The Impact of Melatonin Lotion on Sleep and Mental Health
Official title: The Impact of Melatonin Lotion on Actigraphy, Sleep Quality, Autonomic Nervous System Indicators, Mood, Anxiety Symptoms, and Side Effects
With another health condition · Anxiety in general or mixed
What is tested:
CAMERA (Context-Aware Multimodal Ecological Research and Assessment)
Who can join:
Ages 18 to 55 · Anxiety, Memory
Where:
1 US site in New York
Sponsor:
Columbia University
Titles on ClinicalTrials.gov
Brief title: Prediction of Anxiety and Memory State
Official title: Developing the Context-Aware Multimodal Ecological Research and Assessment (CAMERA) Platform for Continuous Measurement and Prediction of Anxiety and Memory State
Recruiting, interventional studies (Phase 2, 3, or 4 studies, plus therapy and device studies that have no phase) whose title and listed conditions are about an anxiety disorder (not anxiety about surgery, a dental visit, a scan, or another procedure) and that have at least one US site, leaving out programs whose late-stage trials failed and records that look out of date (primary completion date passed and no update in the past 6 months). Up to 50 are shown, balanced across anxiety types and treatment kinds (at most 2 per main intervention), then ranked by phase, number of US sites, and size. Phase 1 safety studies and studies with no US site are left out here but appear on ClinicalTrials.gov. Study details change often; always check the study page and contact the study team to confirm who can join. This site does not enroll anyone.