Psychological Stress

21

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

Condition / disease
Location
Status: Not yet recruiting

Effect of Mandala Coloring on Menopausal Attitude, Perceived Stress and Mindfulness

Menopause is a natural life stage associated with hormonal changes that may affect women physically and psychologically. During this period, women may experience increased stress levels, negative attitudes toward menopause, and decreased mindfulness. Mandala coloring is a structured art-based intervention that may promote relaxation and improve psychological well-being. This randomized controlled trial aims to evaluate the effect of mandala coloring on attitudes toward menopause, perceived stress, and mindfulness levels among menopausal women.

Participants needed: 140
Trial details
Age: 45-55Biological sex: FemaleType: InterventionalSponsor: Ondokuz Mayıs UniversityUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Women aged 45-55 years [+3]

Diagnosed psychiatric or cognitive disorders [+4]

Status: Recruiting

COVID-19 Pandemic Impact on Alcohol (PIA) - A Natural History Study

Background: The SARS-CoV-2 virus has caused a pandemic infection called COVID-19. It is a global threat to people, communities, and health systems. Researchers are concerned about the mental health effects of the pandemic. They want to learn more about how it is affecting people s alcohol use and problems, and how it may continue to affect them over time. Objective: To study the impact of the COVID-19 pandemic on alcohol use and consequences in individuals across the spectrum of alcohol use and those with alcohol use disorder. Eligibility: Participants who have been screened under the NIAAA Screening, Assessment and Management Protocol (14-AA-0181) Design: Participants will complete a baseline survey by phone. It will ask about alcohol use, alcohol dependence, and stress. It covers 2 time periods: the 12 months before the pandemic started and the time since it started. Participants will get an ID code and a link to an online survey. They will complete the online survey within a week of the phone survey. Participants will complete a series of online surveys over 24 months. For the first year, surveys will be completed weekly for the first 4 weeks, then biweekly for the next 8 weeks, and then every 1-2 months for the rest of the year. For the second year, surveys will be completed every 6 months. Surveys will cover the following topics: * Alcohol use and its consequences * Other substance use * Stress * Impact of the COVID-19 pandemic * Pain * Physical health * Sleep * Quality of life. Because the course of the pandemic may change, the frequency of the surveys may change. Participation lasts 2 years.

Participants needed: 1,500
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: National Institute on Alcohol Abuse and Alcoholism (NIAAA)Updated: Jun 24, 2026Locations: 1
Eligibility criteria

Participants who have enrolled in the NIAAA Natural History Protocol (14-AA-0181... [+1]

Status: Not yet recruiting

Theta Healing-Based Intervention in Women With Polycystic Ovary Syndrome

This randomized controlled study aims to evaluate the effect of a Theta Healing-based intervention on fertility concerns, self-compassion, and body image in women diagnosed with Polycystic Ovary Syndrome (PCOS). Participants will be randomly assigned to intervention and control groups. The intervention group will receive a structured 5-day Theta Healing-based online intervention program, while the control group will continue routine care. Outcome measures will be assessed at baseline and 6 weeks after the intervention.

Participants needed: 142
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Ankara Medipol UniversityUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Women aged 18-45 years [+4]

Diagnosed psychiatric disorder [+3]

Status: Not yet recruiting

NeuroFinance Human Stress Trial During Financial and Informational Volatility

The NeuroFinance Human Stress Trial (NFHST-2026-001) is a decentralized observational clinical study designed to evaluate how financial market volatility, economic uncertainty, digital media exposure, and information-driven stress environments affect human physiologic and behavioral health. Participants will undergo remote monitoring using wearable biosensors, cardiovascular telemetry devices, sleep tracking systems, heart rate variability monitoring, and behavioral analytics platforms. The study will use artificial intelligence and machine learning systems to analyze relationships between external financial and informational events and biologic stress responses, including autonomic nervous system activity, sleep disruption, cardiovascular strain, emotional resilience, and inflammatory signaling. The goal of the study is to develop predictive digital biomarkers and AI-assisted forecasting systems capable of identifying stress-related physiologic deterioration before clinical manifestation.

Participants needed: 2,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Truway Health, Inc.Updated: Jun 3, 2026Locations: 1Duration: 24 Months
Eligibility criteria

Adults age 18 years and older. [+7]

Individuals unable or unwilling to provide informed consent. [+5]

Status: Recruiting

Psychosocial, Environmental, and Chronic Disease Trends in Puerto Rico

The overall goal is to identify trends and longitudinal associations in psychosocial, food-related, and cardiometabolic risk factors that can guide public health priorities and future research needs aimed at reducing cardiovascular-related disparities in Puerto Rico. To this end, investigators will establish 'PROSPECT: Puerto Rico Observational Study of Psychosocial, Environmental, and Chronic disease Trends', an island-wide, longitudinal population cohort of 2,500 adults (30-75 years) in PR recruited with a community-wide sampling strategy, and assessed in a network of several partner clinics across the island. The study will collect comprehensive data on multiple psychosocial, dietary, and food-related factors, CVD biological markers, and medical record data, with follow-up at 2-years, and will assess variations by urban-rural area and by timing before-after Maria.

Participants needed: 2,500
Trial details
Age: 30-75Biological sex: AllType: ObservationalSponsor: Harvard School of Public Health (HSPH)Updated: May 5, 2026Locations: 1
Eligibility criteria

Age 30-75 years old at the time of enrollment [+4]

Status: Recruiting

Health Surveillance at Constructor University Bremen (CUB) and Among HAW-Hamburg Employees

The aim of Health Surveillance is to analyze and describe the state of health of students at Constructor University, key influencing factors and individual resources by using mixed-method design.

Participants needed: 363
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Jacobs University Bremen gGmbHUpdated: May 1, 2026Locations: 2
Eligibility criteria

English language skills [+4]

Illiteracy [+1]

Status: Recruiting

Effect of Ashwagandha Root Extract on Stress, Anxiety, and Sleep Quality in Adults Experiencing Minority Stress

Sexual and gender minority adults often experience elevated levels of chronic stress due to stigma, discrimination, and social adversity, commonly referred to as minority stress. This persistent stress is associated with increased anxiety, mood disturbances, impaired sleep quality, and reduced quality of life. There is a need for safe, non-pharmacological interventions that can support mental well-being in this population. This randomized, double-blind, placebo-controlled study is designed to evaluate the efficacy and safety of Ashwagandha (Withania somnifera) root extract in reducing stress and improving anxiety and sleep quality in adults experiencing minority stress. A total of 80 adults aged 18 to 45 years who self-identify as sexual or gender minorities and report moderate to high perceived stress will be enrolled. Participants will be randomly assigned to receive either Ashwagandha root extract (300 mg capsules taken twice daily) or an identical placebo for 8 weeks. Efficacy will be assessed using validated psychological and quality-of-life questionnaires, including the Perceived Stress Scale, Depression Anxiety Stress Scale, Pittsburgh Sleep Quality Index, and other mood and minority stress measures. Salivary cortisol will be measured as a biological marker of stress. Safety will be evaluated through monitoring of adverse events throughout the study.

Participants needed: 80
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: SF Research Institute, Inc.Updated: Apr 27, 2026Locations: 1
Eligibility criteria

Self-identified as a sexual or gender minority (e.g., lesbian, gay, bisexual, tr... [+3]

Current psychiatric diagnosis (e.g., major depressive disorder, bipolar disorder... [+3]

Status: Not yet recruiting

Short-Term Mindfulness Intervention for Anxiety and Maternal Attachment in NICU Mothers

This randomized controlled study aims to evaluate the effects of a short-term mindfulness-based stress reduction (MBSR) program on anxiety levels and maternal attachment in mothers whose infants are admitted to the Neonatal Intensive Care Unit (NICU). A total of 33 mothers will be recruited and assigned to intervention and control groups. The intervention group will receive a structured four-session mindfulness program, while the control group will receive standard care. Data will be collected using the Maternal Attachment Scale and the State-Trait Anxiety Inventory. The findings are expected to provide evidence on the effectiveness of mindfulness-based interventions in reducing anxiety and improving maternal-infant bonding during the postpartum period.

Participants needed: 66
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: Apr 9, 2026
Eligibility criteria

Not listed

Status: Not yet recruiting

Exploring the Decision to Drink (More) Alcohol Following Manipulations of Stress and Social Context

This preregistration documents an experiment examining the effects of acute stress and social context on alcohol-related decision-making. The study uses a 2x2 factorial design (stress vs. control × social vs. alone) with dyadic recruitment.

Participants needed: 160
Trial details
Age: 21-50Biological sex: AllType: InterventionalSponsor: University of WashingtonUpdated: Feb 6, 2026
Eligibility criteria

Drinking alcohol at least once a week [+1]

Currently pregnant or trying to become pregnant [+4]

Status: Recruiting

Effectiveness of a Waitlist App "Stappvoorstap" During Mental Healthcare Waiting Times

This study evaluates the effectiveness of Stappvoorstap, a mobile self-management application designed for adults on mental health waiting lists in the Netherlands. The app helps users monitor daily stress levels, recognize personal stress patterns, and provides coping strategies, relaxation exercises, and supportive resources. Using a multiple baseline single-case experimental design, participants use the app for 4 weeks while completing weekly questionnaires measuring perceived stress, coping self-efficacy, and quality of life. The study aims to determine whether the app can reduce stress and improve wellbeing during the waiting period before mental healthcare treatment begins.

Participants needed: 54
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: GGZ CentraalUpdated: Feb 5, 2026Locations: 1
Eligibility criteria

Currently on a waiting list at a mental health organization in the Netherlands. [+3]

Currently enrolled in another medical-scientific research study

Status: Not yet recruiting

Horse-assisted Intervention, Heart Rate Variability & Stress

In this study, the effects of an animal-assisted intervention on people with increased stress levels are investigated. The data collected will be compared with those of participants with high stress levels but without animal-assisted intervention (participants only observe nature) and with a control group consisting of people without stress exposure. The study will be performed in the following setting: Questionnaire examination on chronic stress, questionnaire on current well-being and heart rate variability (HRV) measurement before the horse-assisted intervention, one HRV measurement and one questionnaire examination (POMS) on current well-being after the horse-assisted intervention, one questionnaire (POMS) on current well-being 5 days after the horse-assisted intervention.

Participants needed: 123
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Medical University of GrazUpdated: Sep 29, 2025Locations: 1
Eligibility criteria

Male, female and diverse [+1]

Animal hair allergies (especially horse hair allergies, fear of horses) [+3]

Status: Recruiting

Cerebrovascular Health and Resilience in Midlife

This study examines cardiovascular responses to a brief psychological challenge under laboratory conditions among adult volunteers. The study volunteers are asked to complete two study sessions. In one session, the volunteers are asked to provide demographic and health-related information via questionnaires and an interview. In that session, volunteers would then be asked to undergo evaluations of their body composition, blood pressure, heart rate, and other signs of cardiovascular function and health. Lastly, volunteers would be asked to take part in a brief and challenging psychological task after a period of rest while cardiovascular activity is measured. In the other session, volunteers are asked to undergo magnetic resonance imaging and to complete neuropsychological tests of memory, attention, and processing speed. In addition to these two sessions, volunteers are asked to complete online questionnaires. The study is designed to examine associations between transient changes in cardiovascular activity induced by the psychological task, measures of overall cardiovascular health, and measures of cerebrovascular health measured by magnetic resonance imaging. Study results are expected to provide new information about the relationships between cardiovascular activity changes to psychological challenges and cardiovascular and cerebrovascular health in adults.

Participants needed: 450
Trial details
Age: 40-59Biological sex: AllType: InterventionalSponsor: University of PittsburghUpdated: Sep 26, 2025Locations: 1
Eligibility criteria

Able to attend 2 study visits at the University of Pittsburgh campus in Oakland... [+1]

Uncontrolled hypertension (systolic blood pressure >160 or diastolic blood press... [+12]

Status: Recruiting

Psilocybin-Assisted Therapy for Intergenerational Trauma

This is an open-label psilocybin-assisted therapy study that will examine the safety and tolerability of psilocybin-assisted therapy in the offspring of genocide survivors with mood and anxiety disorders. The study will also investigate the efficacy of psilocybin-assisted therapy in reducing symptoms such as depression, anxiety and stress, as well as changes to the psychological effects of parental exposure to genocide, and changes to psychological resilience.

Participants needed: 100
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Rachel YehudaUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Age at least 18 years old at time of signing the informed consent [+12]

Not able to give adequate informed consent. [+10]

Status: Not yet recruiting

Effect of Adding Progressive Muscle Relaxation to Physical Therapy Program on Fatigue, Mobility and Stress Among Individuals With Traumatic Lower Limb Amputation in the Gaza Strip

Lower limb amputation is a life-altering condition with profound physical and psychological consequences, including fatigue, impaired mobility, stress, and asymmetrical weight-bearing. These challenges are particularly severe in conflict-affected settings like the Gaza Strip, where access to rehabilitation services is limited. This study aims to evaluates the effect of adding Progressive Muscle Relaxation (PMR), a simple and cost-effective relaxation technique, to standard physical therapy on Fatigue, mobility, weightbearing distribution and stress outcomes among adults with unilateral traumatic lower limb amputation in Gaza. Study design: RCT with 60 participants will be randomly assigned to either (1) a control group receiving standard physiotherapy or (2) an intervention group receiving standard physiotherapy plus PMR. Outcomes will be measured using validated instruments: Fatigue Severity Scale (FSS), 2-Minute Walk Test (2MWT), Perceived Stress Scale (PSS-10), and dual bathroom scale method for weight-bearing distribution. Assessments will be conducted at baseline, post-intervention (6 weeks), and follow-up (8 weeks). The study aims to determine whether integrating PMR into rehabilitation improves fatigue reduction, functional mobility, stress management, and weight-bearing symmetry compared to physiotherapy alone. Findings will contribute to evidence-based rehabilitation strategies for amputees in low-resource, high-stress environments.

Participants needed: 60
Trial details
Age: 18-59Biological sex: AllType: InterventionalSponsor: Marah RadiUpdated: Aug 24, 2025Locations: 1
Eligibility criteria

Adults aged 18 to 59 years. [+2]

Severe comorbidities (e.g., uncontrolled cardiovascular disease). [+2]

Status: Recruiting

RELIEF OF PSYCHOEMOTIONAL STRESS USING XENON SEDATION

The goal of this clinical trial is to propose for implementation and evaluate the effectiveness of xenon sedation for the relief of psychoemotional stress disorder before the operation of refractive laser vision correction patients with high anxiety and stress instability who underwent xenon analgosedation before refractive laser vision correction. The main question\[s\] it aims to answer are: 1. To develop a method of xenon sedation in patients with a high level of psychoemotional stress before surgery - refractive laser vision correction. 2. To evaluate the effect of inhaled xenon anesthesia in a sub-narcotic dose on the duration of surgery, satisfaction of surgeons and patients with anesthesia, the level of postoperative pain in patients in comparison with anxiolytics. The following will be studied: the level of preoperative anxiety, the dynamics of glycemia and blood cortisol levels, heart rate variability, electrical microamplitudes of the ECG signal, the anti-stress and analgesic effect of xenon. If there is a comparison group: the researchers will compare \[the group with xenon sedation and the control group\] to see if there is \[an anti-stress effect of xenon in patients before laser vision correction\].

Participants needed: 140
Trial details
Phase: Early Phase 1Age: 18-45Biological sex: AllType: InterventionalSponsor: The S.N. Fyodorov Eye Microsurgery State InstitutionUpdated: Jun 27, 2025Locations: 1
Eligibility criteria

upcoming operation ReLEx® SMILE; [+2]

Status: Recruiting

Effect of Aerobic Exercise With Synchronous Music on Functions Among Medical Students

Researchers invite participants to volunteer to participate in this cross-sectional, interventional study. This research examines the effects of 8-week aerobic exercise of different intensities combining synchronized music on psychology, attention, and executive function among Chinese college students, and also validates the reliability and validity of the Chinese version of Brief College Student Hassles Scale, the Perceived Stress Scale for Medical Students, Brief Multidimensional Students'Life Satisfaction Scale, Positive Thinking Skills Scale, Attentional Function Index, Procrastination Assessment Scale-Student and Behavioral Assessment of the Dysexecutive Syndrome-College version, providing a research basis for aerobic exercise to improve the cognitive function and mental health level of Chinese college students. Participants will be invited to participate in the intervention study, in which participants will be assigned to the intervention group and control group. Participation in this study will last approximately 8 weeks for a total of 24 sessions, 40 minutes each session, and participants will not be forced to participate in this study if they do not wish to. This study will include up to 134 participants who will be assigned to the intervention and control groups in a randomized manner.

Participants needed: 134
Trial details
Biological sex: AllType: InterventionalSponsor: Universiti Sains MalaysiaUpdated: Mar 26, 2025Locations: 1
Eligibility criteria

Medical students willing to participate in aerobic training [+3]

History of major depressive disorder in the past 6 months [+2]

Status: Recruiting

A Randomized Controlled Evaluation of a Compassion-course for Healthcare Professionals

The aim is to investigate whether an internet-based compassion course of five modules contributes to reducing stress of conscience and work-related stress, increase the experience of professional quality of life and self-compassion in healthcare professionals.

Participants needed: 548
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: Linnaeus UniversityUpdated: Mar 19, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Trauma and Cardiometabolic Health in an American Indian Community

Volunteers for the study are asked to participate in two laboratory sessions. In the first laboratory session, volunteers are asked to provide a blood sample which will be used to measure factors related to health. Participants also complete questionnaires related to demographic and health-related information and undergo evaluations of their body composition. In the second laboratory visit, participants are asked to have cardiovascular, neuroendocrine, and inflammatory activity measured during a brief period of rest and during a short challenging psychological task. Participants will also complete questionnaires. The study is designed to examine the associations between experiences such as trauma and resiliency with changes in bodily systems during a challenge and current health.

Participants needed: 400
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Montana State UniversityUpdated: Mar 17, 2025Locations: 1
Eligibility criteria

18-40 years [+2]

Uncontrolled hypertension

Status: Recruiting

The Associations of Psychological Stress With Therapy Efficacy and Prognosis of Lung Cancer (STRESS-LUNG)

This is the prospective, observational cohort study (STRESS-LUNG) to explore the associations of psychological stress with progression, efficacy of immune checkpoint inhibitors (ICIs) and prognosis of Lung Cancer. The participants including the patients diagnosed with advanced non-small-cell lung cancer (NSCLC) who received the first-line therapy or neoadjuvant therapy of ICIs; patients diagnosed with advanced small-cell lung cancer (SCLC) receiving the first-line therapy ICIs; patients diagnosed with early small-cell lung cancer (SCLC) receiving surgery.

Participants needed: 750
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Second Xiangya Hospital of Central South UniversityUpdated: Feb 25, 2025Locations: 1Duration: 5 Years
Eligibility criteria

Age ≥ 18 years; [+7]

Epidermal growth factor receptor (EGFR)-sensitizing mutation and/or anaplastic l... [+44]

Status: Not yet recruiting

Parental Stress and Attachment in Preterm Infants

Introduction: Advances in neonatology mean a significant reduction in mortality in premature infants as well as an increase in the risk of morbidity in the medium, short and long term. Furthermore, previous studies have linked prematurity, as an associated risk factor, with possible alterations in the bonding between the child and his or her mother in the first years of life. The possible impact that the stay in the neonatal unit may have on the mental health of the parents is noted. In fact, several studies have shown that the hospital environment of neonatal units may contribute to increased stress and anxiety in mothers. On the other hand, prematurity is one of the causes of referral to Child Development and Early Care Centres, to address their development in the first years of life, as well as for family support. One of the functions of early childhood professionals is to guarantee the development of a secure attachment between the child and his or her caregivers. Little is known about whether maternal stress levels can influence mother-child interactions and thus influence the attachment relationship in the early years of life. Objective: to analyse the association between mothers' stress level due to preterm birth and attendance at a Child Development and Early Care Centre and child development and patterns of mother-child interactions.

Participants needed: 60
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Cardenal Herrera UniversityUpdated: Feb 7, 2025Locations: 1Duration: 1 Year
Eligibility criteria

Children born under 37 weeks of gestation, [+1]

Status: Not yet recruiting

Effectiveness of Stress Self-management Health Education Based on IMB Theory Among Nursing Students

The aim of this cluster randomized controlled study is to test the effectiveness of IMB stress self-management health education on nursing students registered in first semester. The main question aims to answer are: Does IMB stress self-management health education program improving stress in nursing students? Researcher will compare wait-list group without any intervention to experimental group which received IMB stress self-management health education, to see if IMB stress self-management health education works to improving stress among nursing students. Participants will Attend IMB stress self-management health education program once a week for 8 weeks. In addition, complete questionnaires at pre-intervention, post-intervention, 1-month post-intervention, 3-months post-intervention, 6-months post-intervention.

Participants needed: 120
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Changzhi Medical CollegeUpdated: Jun 4, 2024
Eligibility criteria

cluster [+7]

cluster [+5]