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Anxiety clinical trials

View clinical trials related to Anxiety.

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NCT ID: NCT06162741 Not yet recruiting - Depression Clinical Trials

Type I Hybrid Effectiveness-Implementation Trial of Primary Care Brief Mindfulness Training for Veterans

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

The VA wants to understand what type of integrative and whole health approaches are helpful for Veterans. The study is comparing two primary care based mental health treatments, a mindfulness class that teaches mindfulness meditation and a problem-solving class that teaches problem-solving skills and how to build resilience, for Veterans who are experiencing symptoms of anxiety, depression, and/or PTSD. The goal of the study is to understand if the classes reduce symptoms of anxiety, depression, and/or PTSD and increase overall functioning.

NCT ID: NCT06162624 Not yet recruiting - Depression Clinical Trials

Pilot Effectiveness Trial of an ACT Self-help Workbook Tailored Specifically for Prisons

Start date: September 2024
Phase: N/A
Study type: Interventional

The goal of this research study is to adapt an ACT-self-help workbook to the prison setting and determine the feasibility acceptability, and effectiveness of this workbook. Participants can expect to be in the study for 13 weeks.

NCT ID: NCT06158763 Recruiting - Depression Clinical Trials

Development and Evaluation of a CBT-based Transdiagnostic Transcultural Web App for Mental Health Problems

WCBT
Start date: December 1, 2023
Phase: N/A
Study type: Interventional

This study aims to (1) develop a CBT-based transcultural, transdiagnostic interactive web app and (2) assess the feasibility, acceptability, and preliminary efficacy of this intervention.

NCT ID: NCT06156852 Completed - Anxiety Clinical Trials

Comparing the Effects of Mindfulness-Based and Cognitive Behavioral-Based Stress Reduction in Medical Students

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

We aimed to compare the effects of the Mindfulness-Based Stress Reduction (MBSR) and the Cognitive Behavioural Stress Reduction (CBSR) group interventions on depression and anxiety symptoms and perceived stress of medical students. 323 medical students applied to participate in one of the group interventions and were assessed with the Mini International Neuropsychiatric Interview. Of these, 253 (77% female, mean age=21.9 ± 2.9 years) were allocated into online MBSR (n=127) and online CBSR (n=126) groups after randomization. Their anxiety and depressive symptoms and perceived stress levels were assessed at baseline and after 8 weeks of interventions.

NCT ID: NCT06156306 Recruiting - Anxiety Clinical Trials

CBT-I Versus CBT-I+ACT for Youths With Insomnia and Anxiety

Start date: December 15, 2023
Phase: N/A
Study type: Interventional

Insomnia in adolescents and youth is a long-standing public health concern due to its high prevalence and association with various physical and mental health problems. Insomnia and psychiatric disorders are highly comorbid and intercorrelated in adolescents. Among all mental disorders, anxiety has been shown to be have high comorbidity with insomnia, affecting approximately 30% of individuals. CBT for insomnia (CBT-I) has been shown to be effective in improving sleep complaints and short-term improvement in mood while previous systematic reviews of interventional studies have demonstrated the effectiveness of acceptance and commitment therapy (ACT) interventions in treating insomnia, both as a primary condition and with other physical and/or mental health comorbidities. This study aims to compare the effect of CBT-I and CBT-I combined ACT in improving anxiety symptoms in youth.

NCT ID: NCT06155838 Enrolling by invitation - Depression Clinical Trials

Reducing Depression and Anxiety Among Teens

Start date: November 27, 2023
Phase: N/A
Study type: Interventional

The objective of this clinical trial is to assess the efficacy of the Early Adolescent Skills for Emotions (EASE) program, a school-based, non-specialist psychosocial intervention developed by the WHO for LMICs, in alleviating Anxiety and Depression among teens aged 13-19. The primary inquiries it seeks to address include: Does the EASE intervention effectively reduce anxiety and depression scores 12 weeks after implementation? - Can the EASE intervention enhance quality of life, improve problem-solving skills, and increase perceived emotional support? - Is the EASE intervention beneficial for enhancing the psychological well-being of parents and fostering positive parent-teen relationships?

NCT ID: NCT06154369 Recruiting - Depression Clinical Trials

JoyPop Mobile Mental Health App With Post-Secondary Students

Start date: November 22, 2023
Phase: N/A
Study type: Interventional

Students within post-secondary education settings are experiencing increasing stress, distress, and mental health difficulties. Many post-secondary education settings have identified student mental health and wellbeing as a priority and yet are struggling to adequately meet the needs of students. This has led to exploring whether technology can be used to help promote mental health and wellbeing among students. The JoyPop app is one mobile mental health app with a growing evidence base. It was developed to support improved emotion regulation - a key challenge among students struggling with distress and mental health difficulties. Using a randomized controlled trial (RCT) design, the primary objective of this research is to determine the effectiveness of the JoyPop app in improving emotion regulation among post-secondary students when compared to no intervention. The secondary objectives are to: (1) Assess change in mental health, wellbeing, and resilience between students in each condition to better understand the app's broader impact; (2) Conduct an economic analysis to determine whether receiving the app reduces other health service use and associated costs; (4) Assess students' perspective on the quality of the JoyPop app.

NCT ID: NCT06153628 Enrolling by invitation - Anxiety Clinical Trials

The Effect of Virtual Reality Glasses on Anxiety Level and Breast Milk Amount

Start date: November 3, 2023
Phase: N/A
Study type: Interventional

Pain, anxiety, nausea, vomiting, etc. In coping with symptoms, virtual reality glasses are recommended as a distraction application. The study was planned to examine the effect of virtual reality glasses applied to mothers whose babies were in the neonatal intensive care unit, on the level of anxiety and the amount of breast milk.

NCT ID: NCT06152211 Not yet recruiting - Anxiety Clinical Trials

Music-Based Interventions, Aging, Alzheimer's Disease

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT06150963 Completed - Pain Clinical Trials

Virtual Reality for the Management of Pain and Anxiety for Outpatient Interventional Radiology Procedures

Start date: June 10, 2021
Phase: N/A
Study type: Interventional

This study explores the use of virtual reality (VR) to reduce pain and anxiety during thyroid biopsies and PICC line insertions under local anesthesia. One group experienced the procedure with VR, while the other group did not. Participants completed questionnaires before and after the surgery to measure pain and anxiety levels. The main goal is to observe if VR can significantly decrease pain and anxiety during these procedures.