Stress

243

Review clinical trials related to Stress. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Ecological Momentary Assessment of State-Dependent Decision-Making and Metacognition Across a Psychopathology Continuum

Background: Making decisions during daily life is a complicated behavior. Even simple choices can be affected by a range of emotions, stresses, and moods. Mental health issues such as depression and anxiety can lead people to make decisions that have negative effects on their lives. Learning how changes in feeling affect a person's decisions may help researchers find ways to help them make more positive choices. Objective: To learn how changes in a person's feelings and emotions affect their decisions. Eligibility: People aged 18 to 55 years who are healthy or who have some level of depressive, anxiety, substance-related, or addictive disorders. Design: All study activities can be done remotely; participants may use a smartphone app, a website, or telehealth. Participants will have a baseline visit. They will complete tasks that require decisions; these tasks are like games they play on their phone. They will also answer questions about their habits, how they feel, their sleep quality, and any problem behaviors. They may wear a smartwatch during the study; it will record data such as their movements and heart rate. For 12 weeks, a study app will prompt participants to respond. They will be asked to answer questions about how they are feeling, any problematic behaviors, or big life events; they will be asked to complete tasks that require making decisions. They may record a video or audio clip describing their day and how they feel. For 3 of the 12 weeks, participants will get prompts up to 6 times per day. For 9 weeks, they will get up to 3 prompts per day. They will have an end-of-study visit to discuss their experiences.

Participants needed: 420
Trial details
Age: 18-55Biological sex: AllType: ObservationalSponsor: National Institute of Mental Health (NIMH)Updated: Oct 7, 2026Locations: 1
Eligibility criteria

Understands study procedures as well as the risks and benefits associated with t... [+4]

Any unstable medical conditions (not well-controlled or are subject to frequent... [+17]

Status: Not yet recruiting

The Effect of Audio-hypnosis on the Academic Performance of Nursing Students.

Exam stress significantly affects the mental health and cognitive functions of nursing students. Audio-hypnosis offers a practical and low-cost intervention. Objective: To evaluate the effect of a single audio-hypnosis session on perceived stress, heart rate, and academic results. Methods: A pilot randomized trial will be conducted with 20 second-year students at ISPITS Safi, divided into an intervention group and a control group (n=10 each). Anxiety (VAS), heart rate (HR), and exam grades were analyzed.

Participants needed: 20
Trial details
Biological sex: AllType: InterventionalSponsor: HASSAN 1st universityUpdated: Oct 7, 2026Locations: 1
Eligibility criteria

Students enrolled in the first year of nursing training at the Higher Institute... [+1]

Students who refuse to participate or do not sign consent. [+3]

Status: Not yet recruiting

PURSUIT: A Technologically Augmented School-based Program to Improve Child Coping and Prevent Substance Use.

The study investigators aim to test an online support platform for Michigan youth aged 8-18 years enrolled in elementary, middle, or high school and their parent/caregiver. The online support platform will be hosted on the Computerized Intervention Authoring System (CIAS) 3.0 and will provide evidence-based cognitive behavioral coping skills for physical (pain) and mental (stress, mood) health symptoms, with additional substance use prevention content for youth aged 12 and older. Evaluations will occur at baseline and then a post assessment approximately 8 weeks later.

Participants needed: 100
Trial details
Age: 8-18Biological sex: AllType: InterventionalSponsor: Michigan State UniversityUpdated: Oct 6, 2026Locations: 1
Eligibility criteria

Aged eight to 18 years [+1]

Age under 8 [+2]

Status: Recruiting

State-dependent Interoception, Value-based Decision-making, and Introspection

Background: Negative emotional states can affect a person s behavior as they make decisions. For example, hunger may make people more impatient; they may then make riskier choices. Other negative emotional states that can change behavior include stress, pain, and sadness. By learning more about how emotions affect thinking and behavior in healthy people, researchers hope to better understand how to identify and treat people with mental disorders. Objective: To learn how negative emotions affect the brain and decision-making behavior. Eligibility: Healthy people aged 18 to 55 years. Design: Participants will have 3 clinic visits in 3 weeks. Participants will fill out questionnaires. They will be asked about their personal history, their personality, and state of mind. For 2 visits, participants will be assigned to different groups. Each group will experience 1 type of emotional stressor: Some participants will watch a video. Some will have to do arithmetic problems. Some will have heat applied to an arm or leg. Some will experience cold by immersing their hand in ice water. For a snack craving test, some will be tempted by food after a 4-hour fast. During these tests, participants will have sensors attached to their bodies. They will be videotaped. Saliva samples will be collected. After the stressors, participants will do tasks on a computer. They will need to make choices. Some participants will perform these decision-making tasks while lying in a brain scanner for functional magnetic resonance imaging. The brain scan involves lying on a table that slides into a cylinder that takes images of the brain. ...

Participants needed: 900
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: National Institute of Mental Health (NIMH)Updated: Oct 2, 2026Locations: 1
Eligibility criteria

Ability of subject to understand and the willingness to sign a written informed... [+2]

Unable to comply with study procedures or follow-up visits [+22]

Status: Not yet recruiting

Talk Parenting Education Program II

The goal of this clinical trial is to learn whether Talk Parenting, a voice-based program delivered through an Amazon Echo Dot (Alexa), can help parents and caregivers of children ages 3-5 years improve challenging bedtime and morning routines. The main questions it aims to answer are: Does using Talk Parenting improve families' bedtime and morning experiences and children's sleep/wake habits? Does using Talk Parenting improve parents' routine-related parenting practices and confidence, strengthen the parent-child relationship, and reduce children's behavior problems and parents' stress? Researchers will compare families who receive Talk Parenting right away to families who wait 6 weeks to receive the program (a waitlist control group receiving usual services during the wait). Participants will: Complete online questionnaires at the start of the study and again about 6 weeks later (and a follow-up questionnaire later in the study). Receive a pre-configured Amazon Echo Dot (to keep) and instructions to use Talk Parenting routines at home, including a bedtime routine, a brief calming routine, and a morning routine (enabled after the first 2 weeks).

Participants needed: 184
Trial details
Age: 3-90Biological sex: AllType: InterventionalSponsor: Oregon Research Behavioral Intervention Strategies, Inc.Updated: Oct 5, 2026Locations: 1
Eligibility criteria

Referred by a participating agency [+5]

Families of target-age children with a developmental disability severe enough th... [+1]

Status: Recruiting

Exercise Effects on the Neurobiology Underlying Stress-related Eating Behaviors in Veterans

The purpose of this study is to learn more about how common lifestyle interventions, such as exercise, affect how our brains respond to performing thinking tasks and to viewing pictures of foods and various other objects. The investigators are also interested in how changes in hormones that might be different in men and women could affect how lifestyle interventions change these brain responses.

Participants needed: 132
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: VA Office of Research and DevelopmentUpdated: Oct 5, 2026Locations: 1
Eligibility criteria

Veteran [+3]

Currently pregnant [+6]

Status: Not yet recruiting

Effects of School-Based Ignatian Examen Meditation on Well-Being, Gratitude, Hope, and Spirituality in Hong Kong Catholic Primary School Students

This study aims to investigate the effects of Ignatian Examen Meditation on students' psychological well-being, gratitude, hope, and spirituality. Specifically, it examines whether participation in Examen Meditation improves emotional well-being by reducing stress, anxiety, and depression, enhancing students' sense of gratitude and hope, and strengthening spiritual development. The study also explores the lived experiences of students and teachers who participate in the programme. Regarding significance, this study addresses the lack of empirical studies examining Examen Meditation in Asian educational settings. The findings will provide evidence regarding the effectiveness of a Catholic contemplative practice in supporting students' mental health and spiritual formation. It may contribute to the development of school-based well-being programmes in Catholic schools by demonstrating the potential benefits of Examen Meditation for psychological well-being, the sense of gratitude and hope and spiritual growth.

Participants needed: 360
Trial details
Age: 9-12Biological sex: AllType: InterventionalSponsor: Chinese University of Hong KongUpdated: Oct 5, 2026Locations: 1
Eligibility criteria

Students aged 9-12 years. [+4]

Students younger than 9 or older than 12. [+2]

Status: Not yet recruiting

Exploring PTSD Symptoms, Barriers and Facilitators to Mindfulness

The purpose of this study is to investigate justice-involved Black/African American female adolescents' (JI BAFAs; N=35) self-reported outcomes: stress, posttraumatic stress disorder (PTSD), recidivism, etc., as well as their parents/caregivers' (P/Cs; N=35) stress and pre- and post- intervention results along with their views of an adapted intervention.

Participants needed: 90
Trial details
Age: 14-90Biological sex: AllType: InterventionalSponsor: University of MichiganUpdated: Oct 2, 2026
Eligibility criteria

Black girls aged 14-18 [+6]

Prisoners per the IRB definition [+5]

Status: Not yet recruiting

Personalized Care for Prenatal Stress Reduction & Prevention of Preterm Birth (PTB) Disparities

The goal of this clinical trial is to learn if a personalized prenatal support program \[(Personalized Toolkit Building a Comprehensive Approach to Resource optimization and Empowerment in Pregnancy \& Beyond, (PTBCARE+)\] works to lower stress and lower the risk of early delivery in pregnant individuals at high-risk for delivering preterm. The main question\[s\] it aims to answer are: * Does the PTBCARE+ patient support program lower patient-reported stress levels during pregnancy? * Does the PTBCARE+ patient support program improve biologic measures of stress during pregnancy? * Does the PTBCARE+ patient support program result in a higher chance of delivering a healthy baby at or close to full term? Researchers will compare people who participate in the PTBCARE+ patient support program to those receive usual care to see if the PTBCARE+ patient support program lowers patient-reported stress, improves biologic measures of stress, and increases the chance of delivering a healthy baby at or close to full term. Participants will be randomly assigned to receive the PTBCARE+ patient support program or usual prenatal care. All participants will be asked to: * complete 2 study visits during pregnancy - including completing electronic surveys, providing a blood and urine sample, measuring the heart rate variability by a clip or the ear or finger, and body composition evaluation using a simple scale-like device. * complete one study visit postpartum that includes completing electronic surveys, and measuring heart rate variability. Blood and urine sample collection and body composition evaluation via InBody scale are optional at the postpartum visit. People who are randomly assigned to receive the PTBCARE+ support program will receive several resources to help them during pregnancy. These things include items such as: * a stress reduction toolkit; * access to an online website that can also be downloaded as a smart phone app; * the option to receive an electronic massage while in clinic, and more. * additional support gifts provided at routine clinical appointments People who are randomly assigned to receive usual prenatal care will not receive any additional support resources from the study during pregnancy.

Participants needed: 1,228
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of North Carolina, Chapel HillUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

Viable, singleton pregnancy, 8+0 to 19+6 weeks, dated by last menstrual period ±... [+18]

Participation in another intervention based clinical trial during pregnancy that... [+23]

Status: Recruiting

How Does the Opioid System Shape Stress and Social Behaviour in Men and Women and What Role Does Childhood Unpredictability Play?

The study aims to investigate sex differences in the effect of mu-opioid receptor (MOR) activation on stress response and social behaviour modulated by early life stress.

Participants needed: 72
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Sara L. KrollUpdated: Sep 28, 2026Locations: 1
Eligibility criteria

Age 18-40 years [+7]

Any current instable medical or neurological condition [+21]

Status: Recruiting

2D:4D Ratio in Relation to Anxiety and Stress Among Anesthesiology Residents

Anesthesiologists are exposed to substantial occupational stress, making their psychological well-being essential for both personal health and optimal patient care. Early identification of mental health disorders among healthcare professionals is important for improving well-being and maintaining healthcare quality.

Participants needed: 116
Trial details
Age: 20-35Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Sep 30, 2026Locations: 1
Eligibility criteria

Any anesthesiologists who voluntarily agreed to participate in the study. [+2]

Incomplete questionnaires and/or irrelevant responses. [+5]

Status: Recruiting

Adapting a Stress Management Intervention to Reduce Cardiovascular Disease Risk

Women living with HIV have 2-4x higher risk for cardiovascular disease compared to women without HIV, with women living with HIV in the Southern US being particularly at risk. While an increased prevalence of traditional risk factors (e.g., hypertension, diabetes, and obesity) partially explain this risk, evidence suggests that increased exposure to structural and social stressors (e.g., poverty, discrimination, and stigma) among women living with HIV in the South negatively contribute to cardiovascular disease disparities through their impact on stress. The Stress Management and Resiliency Training (SMART) program is an effective, evidence-based intervention proven to improve resiliency to environmental stressors and reduce the physiologic responses to stress which contribute to cardiovascular disease. While the SMART program has demonstrated efficacy in a wide range of populations and settings, it has not been designed for or tested among women living with HIV in the South, where unique cultural and faith-based context may diminish the uptake and value of the intervention to mitigate cardiovascular disease risk. The purpose of this study is to adapt the evidence-based SMART program in consideration of the needs and contexts of women living with HIV in the Southern US and pilot the adapted intervention to establish the feasibility, acceptability, and preliminary impact of the adapted intervention to reduce stress and mitigate cardiovascular disease risk among this population.

Participants needed: 48
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of Alabama at BirminghamUpdated: Sep 28, 2026Locations: 1
Eligibility criteria

cis-gender females at least 18 years of age [+2]

severe mental illness [+2]

Status: Recruiting

Diaphragmatic and Box Breathing on Heart Rate Variability and Perceived Stress

The goal of this clinical trial is to learn if diaphragmatic breathing and box breathing work to enhance resilience and manage stress in physical therapy students. It will also learn about their effects on overall physiological and psychological parameters. The main questions it aims to answer are: Do these breathing techniques improve heart rate variability (HRV)? How do these interventions affect participants' perceived stress levels, cognitive performance, and academic achievement? Researchers will compare diaphragmatic breathing and box breathing to a control group to see if these non-invasive methods work to improve physiological adaptation and manage stress. Participants will: Be randomly assigned to practice diaphragmatic breathing, practice box breathing, or join a control group Have their heart rate variability (HRV) measured as a primary sign of physiological adaptation Complete assessments to evaluate their perceived stress, cognitive performance, and academic achievement

Participants needed: 60
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Sep 28, 2026Locations: 1
Eligibility criteria

Academic Status: Currently enrolled, full-time undergraduate Physical Therapy st... [+4]

Pre-existing Breathing Expertise: Individuals with professional training in yoga... [+7]

Status: Not yet recruiting

Photobiomodulation, Heart Rate Variability, and Acute Stress

Photobiomodulation (PBM) is a form of light therapy that uses red or near-infrared light to influence biological processes. In prior studies, PBM has been shown to improve various physiological functions, including tissue repair, inflammation, and cognitive performance. However, little is known about its impact on autonomic nervous system regulation. Thus, the goal of this study is to evaluate the effects of PBM on vagal activity, as measured by heart rate variability (HRV), in healthy adults undergoing experimental stress.

Participants needed: 40
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: Brigham and Women's HospitalUpdated: Sep 24, 2026
Eligibility criteria

Healthy adults, aged 18-64 years [+2]

Taking medications that could significantly influence autonomic function [+2]

Status: Recruiting

Effects of Probiotic Supplementation on Stress and Anxiety in Students

This randomized, double-blind, placebo-controlled study evaluates the efficacy and safety of an 8-week probiotic supplementation (Lactobacillus plantarum LP140 and Bifidobacterium breve BB010 in total daily dose 1 × 10¹⁰ CFU or matching placebo) in reducing perceived stress and anxiety, and improvement related psychological parameters in healthy university students during the examination period. The primary outcome is the change in Perceived Stress Scale (PSS-10) score at week 5 and week 8 of interevention compared to placebo. The secondary outcomes are the changes in DASS-21 subscales (Stress, Anxiety, Depression), State-Trait Anxiety Inventory - State version scale (STAI-S), Sense of Coherence Scale (SOC-29), Pittsburgh Sleep Quality Index (PSQI), self-reported gastrointestinal symptoms (Likert scale) and incidence of adverse events during the 8-week lasting interventional study.

Participants needed: 200
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Nordic Biotic Sp. z o.o.Updated: Sep 25, 2026Locations: 1
Eligibility criteria

Male or female students aged 18-40 years [+5]

Irritable bowel syndrome (Rome IV criteria) or any chronic intestinal disease (i... [+10]

Status: Not yet recruiting

MIND-WELL Intervention

Lung cancer patients often go through more than one type of treatment, such as chemotherapy, radiation, and immunotherapy. These treatments can lead to several transition periods, which may increase stress and leave some needs unmet for patients and their family caregivers. The purpose of this study is to find out whether a program that includes mindfulness (stress reduction) and education is helpful, acceptable, and practical for lung cancer patients and their family caregivers. We also want to learn if this program helps them feel better prepared during these transitions.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of ArizonaUpdated: Sep 24, 2026Locations: 1
Eligibility criteria

Lung cancer patients aged 18 years or older who are currently receiving or sched...

Inclusion Criteria: Family caregivers aged 18 years or older who are providing a... [+1]

Status: Not yet recruiting

Radicle Relaxation™ CIX: A Study Assessing the Impact of Health and Wellness Products on Stress and Related Health Outcomes

Radicle Relaxation™ CIX: A randomized, double-blind, placebo-controlled study assessing the impact of health and wellness products on stress and related health outcomes

Participants needed: 550
Trial details
Age: 21-105Biological sex: AllType: InterventionalSponsor: Radicle ScienceUpdated: Sep 23, 2026Locations: 1
Eligibility criteria

Adults, at least 21 years of age at the time of electronic consent, inclusive of... [+18]

Status: Not yet recruiting

Evaluation and Implementation of Digital Health Ecosystem in Academic Health Center

Mobile health technologies, such as smartwatches, wearable sensors, and digital applications, have the potential to support healthier lifestyles and improve the management of health conditions. These technologies can collect information on physical activity, sleep, heart rate, heart rate variability, respiratory rate, and other health indicators. However, integrating data from these devices into routine health care and electronic health records remains challenging, particularly in primary care settings and remote communities. The purpose of this study is to evaluate the implementation and feasibility of an integrated digital health ecosystem that combines wearable monitoring using smartwatches with a secure digital platform. The ecosystem is designed to collect, transmit, and display health information in a way that may support patients, health care providers, and researchers. Participants will use wearable technologies and complete questionnaires while health-related information is collected through the digital platform. The study will assess the usability, acceptability, interoperability, and feasibility of implementing this technology in real-world settings, including primary care clinics and remote communities. The study will also explore the potential use of wearable-derived physiological data to support the assessment, monitoring, and management of physiological and psychological stress. The knowledge gained from this study may help improve the integration of digital health technologies into routine care, support self-management and preventive health strategies, and facilitate access to health monitoring in underserved environments. Findings may also contribute to the development of digital health solutions for isolated and extreme environments, including future space exploration missions. This research aligns with priorities identified by the Canadian Space Agency to advance technologies that support safe, healthy, and productive human activities in remote and extreme environments on Earth and during future space missions beyond low Earth orbit.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Laval UniversityUpdated: Sep 21, 2026Locations: 2
Eligibility criteria

Adults aged 18 years or older. [+6]

Severe cognitive impairment or any condition preventing informed consent or stud... [+4]

Status: Recruiting

Effects of Beef-Forward Ready-to-Eat Meals on Recovery Following Simulated Fire Suppression Activities

This clinical trial aims to determine whether consuming beef-based protein before and after physically demanding simulated firefighting activities improves recovery, physical performance, and cognitive performance in healthy adult firefighters. The study will also compare beef-based protein meals with plant-based protein meals. The main questions this study aims to answer are: Does consuming beef-based protein reduce changes in markers of muscle damage, physiological stress, and muscle soreness following a simulated fire ground test? Does consuming beef-based protein help maintain or improve physical and cognitive performance during recovery compared with plant-based protein? Researchers will compare two ready-to-eat meal conditions: beef-based protein, and plant-based protein. Each participant will complete all two conditions in a randomized crossover design, with 14 to 21 days between conditions.

Participants needed: 20
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Sam Houston State UniversityUpdated: Sep 16, 2026Locations: 2
Eligibility criteria

18 to 60 years of age [+5]

Younger than 18 years or older than 60 years [+8]

Status: Not yet recruiting

Racism-related Stress and Objective Short-sleep as Moderators of Treatment Effect in Cognitive Behavioral Therapy for Insomnia

The purpose of this study is to understand whether Black participants with insomnia with objective short-sleep (ISSD) experience less symptom improvement in response to Cognitive Behavioral Therapy for Insomnia (CBTi) than Insomnia with Normal Sleep Duration (INSD) and whether this difference is driven by downstream racism-related stress and experiences. The investigators propose an innovative pragmatic open-label design in which Black participants with insomnia undergo a standard 6-week protocol of digital CBTi. The investigators will quantify ISSD using wireless EEG and will gather high-resolution naturalistic data of racism-related stress using random smartphone prompts and Ecological Momentary Assessments (EMA).

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Johns Hopkins UniversityUpdated: Sep 10, 2026
Eligibility criteria

Non-Hispanic Black adults [+3]

Current alcohol or substance use issues, [+8]

Status: Recruiting

Study of Cannabidiol and Neuroimaging on Stress

Dysregulation in stress responsivity is a growing psychiatry-transdiagnostic fundamental phenomenon, with limited therapeutic strategies. With the legalization of medical and recreational cannabis, many people consume cannabidiol (CBD; a nonintoxicating cannabinoid) to alleviate stress response, without the benefit of scientific guidance. To address this gap, the investigators propose a rigorous translational neuroscience study in a clinical high-risk population to define the roles of CBD in stress response with mechanisms of mesocorticolimbic-network function and hierarchy, neurometabolic, endocrine, and behavior, building upon convergent evidence from animal models and human evidence from our laboratories.

Participants needed: 160
Trial details
Phase: Phase 1, Phase 2Age: 18-25Biological sex: AllType: InterventionalSponsor: Icahn School of Medicine at Mount SinaiUpdated: Sep 10, 2026Locations: 1
Eligibility criteria

Ability to understand and give informed consent. [+5]

Have a medical condition that would make study participation unsafe, and/or whic... [+13]

Status: Recruiting

Effects of Pork Protein on Recovery Following Simulated Fireground Activity

The goal of this clinical trial is to learn whether consuming pork-based protein before and after physically demanding simulated firefighting activities can improve recovery, physical performance, and cognitive performance in healthy adult firefighters. The study will also compare pork-based protein meals with plant-based protein meals and a carbohydrate-focused control condition. The main questions this study aims to answer are: Does consuming pork-based protein reduce changes in markers of muscle damage, physiological stress, and muscle soreness following a simulated fire ground test? Does consuming pork-based protein help maintain or improve physical and cognitive performance during recovery compared with plant-based protein and a carbohydrate-focused control condition? Researchers will compare three ready-to-eat meal conditions: pork-based protein, plant-based protein, and a carbohydrate-focused control condition. Each participant will complete all three conditions in a randomized crossover design, with 14 to 21 days between conditions.

Participants needed: 20
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Sam Houston State UniversityUpdated: Sep 15, 2026Locations: 2
Eligibility criteria

18 to 60 years of age [+5]

Younger than 18 years or older than 60 years [+8]

Status: Recruiting

Impact of Peanut Consumption on Stress, Immune Function, Inflammation, and Cardiovascular Health in High-Stress Individuals

The purpose of this research is to determine whether peanut consumption improves indicators of cardiovascular disease (CVD) risk in human subjects following the consumption of study foods.

Participants needed: 70
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: USDA, Western Human Nutrition Research CenterUpdated: Sep 11, 2026Locations: 1
Eligibility criteria

Males and females [+3]

Less than 18 and over 65 years old [+28]

Status: Recruiting

The Effect of Using a Stress Ball During Transrectal Ultrasound-Guided Prostate Biopsy on Anxiety, Pain, and Hemodynamic Variables

The Effect of Using a Stress Ball During Transrectal Ultrasound-Guided Prostate Biopsy on Anxiety, Pain, and Hemodynamic Variables

Participants needed: 72
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: Mersin UniversityUpdated: Sep 9, 2026Locations: 1
Eligibility criteria

Aged 18 years or older, [+7]

Under 18 years of age, [+7]

Status: Recruiting

The Impact of 12-week Ashwagandha Supplementation Induced by Resistance Training on Strength, Levels of Neurotrophic and Stress Response Proteins, Oxidative and Psychological Stress, and Cognitive Function in Physically Active Male Adults

This clinical trial will study the effects of Ashwagandha (Withania somnifera), a natural plant extract, on physical and mental health in adult men. Ashwagandha is known for its potential to reduce stress, support hormonal balance and improve sleep and physical performance. The study will explore how taking Ashwagandha for 12 weeks, with resistance training, affects various health markers such as stress hormones, brain function, muscle strength, body composition, sleep quality, and cognitive abilities. Participants will be healthy, non-smoking men aged 25-40, with regular resistance training experience. They will be randomly assigned to one of two groups: (1) weight training + Ashwagandha, (2) weight training + placebo. The study is double-blinded, meaning neither participants nor researchers will know who is receiving Ashwagandha or placebo. Participants will: * Take Ashwagandha or a placebo every day for 12 weeks * Train in the gym three times a week Researchers will assess changes in blood markers (like cortisol, testosterone and BDNF - brain-derived neurotrophic factor), physical performance (muscle strength and endurance), sleep quality, stress perception and cognitive function before and after the 12-week period. The goal is to better understand how Ashwagandha works.

Participants needed: 40
Trial details
Age: 25-40Biological sex: MaleType: InterventionalSponsor: Gdansk University of Physical Education and SportUpdated: Sep 3, 2026Locations: 1
Eligibility criteria

Minimum 6 months of consistent resistance training experience [+3]

History of cardiovascular events, liver disorders, or psychiatric illness [+3]