Heart Rate Variability

20

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

Condition / disease
Location
Status: Recruiting

JOB STRESS in OPHthalmology Physicians and Residents

Ophthalmology physicians and residents work under stress conditions during night emergency ophthalmology shifts. Under time pressure, that is a characteristic of the urgency of care, they must use all their cognitive resources to make an accurate diagnosis and to provide accurate decisions, with sometimes surgical emergency acts. In addition, in France, they work at night following by an usual day work, and they can also work 48 consecutive hours during weekends, followed by a work day … i.e. 60 consecutive hours of work … Long working hours with a short recovery time has been demonstrated to be a major factor of stress and fatigue. Even if not demonstrated on ophthalmologists, those working conditions may contribute to symptoms of mental exhaustion and physical fatigue (sleep deprivation), often accompanied by a loss of motivation at work. This may leads to a feeling of loss of time control; stress can also distort the perception of time and leads to hasty actions or delayed decision-making. The combined effects of stress, feelings of loss of time control, and fatigue necessarily have an impact on work performance and work quality, with a high risk of medical error. Moreover, prolonged stress may expose ophthalmologists to a higher risk of multiple diseases, predominantly systemic inflammation and coronary heart disease. The main hypothesis is that prolonged work (up to 60 consecutive working hours) may impact on HRV, comparatively to a typical working day.

Participants needed: 30
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University Hospital, Clermont-FerrandUpdated: Jun 16, 2026Locations: 1
Eligibility criteria

Ophthalmologists defined as physicians who completed the ophthalmology DES (Spec... [+3]

Participant refusal to participate [+1]

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: Not yet recruiting

Comparison of Heart Rate Variability Analysis Durations and Their Relationship With Blood Pressure

This observational study aims to compare heart rate variability (HRV) parameters obtained from different analysis durations in healthy adults and to examine how these parameters relate to resting blood pressure values. HRV is a noninvasive measure commonly used to assess autonomic nervous system activity. Standard short-term HRV analysis is typically based on 5-minute recordings, but shorter and longer analysis durations are also used in research and practice. This study will evaluate whether HRV values derived from 1-minute, 5-minute, 10-minute, and 20-minute analysis windows differ from one another and whether their relationships with systolic blood pressure, diastolic blood pressure, and mean arterial pressure change according to analysis duration. Participants will attend a single study visit. After a rest period, resting blood pressure and pulse will be measured, and a continuous HRV recording will be obtained using a chest strap device. The study is designed to provide methodological information on the comparability of different HRV analysis durations under the same physiological conditions.

Participants needed: 40
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Sinop UniversityUpdated: Apr 15, 2026Locations: 1
Eligibility criteria

Healthy adults aged 18 to 40 years [+3]

History of diagnosed cardiovascular, neurological, or autonomic nervous system d... [+4]

Status: Recruiting

Auricular Vagus Stimulation and Heart Rate Variability

Transcutaneous electrical stimulation of the auricular vagus nerve (TENS) is a promising method of neuromodulation of the autonomic nervous system in patients with various pathologies. The use of this method requires the determination of a reliable biomarker of successful activation of the vagus nerve using TENS. Currently, most studies focus on the assessment of heart rate variability (HRV) as a marker of the functioning of the autonomic nervous system. Despite the physiological justification of HRV as a biomarker for TENS, the data on the effects of TENS on HRV are ambiguous. In some studies, a significant decrease in the ratio of spectral characteristics (LF/HF) in active TENS was found in comparison with fictitious stimulation (sham), which indicated an increase in the parasympathetic component of HRV. However, other studies have not revealed an increase in HRV.

Participants needed: 600
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Bakulev Scientific Center of Cardiovascular SurgeryUpdated: Jun 18, 2025Locations: 3
Eligibility criteria

Sinus rhythm at the time of registration

Frequent ventricular / supraventricular extrasystole, 2d/3d degree AV Block [+3]

Status: Recruiting

Exploring the Relationship Between Heart Rate Variability (HRV), Training Load, and Endurance Performance

The ability of smart phones, aided by wearable devices (e.g. smart watches), to collect a variety of data, including physical activity, heart rate, and other exercise metrics, may provide a unique opportunity to understand real-world variability. The primary objective of this study is to test user engagement, app functionality, and feasibility of the newly developed Gatorade Sports Science Institute (GSSI) Labs App to conduct Real-World research studies. The secondary purpose of this study is to determine if Training Intensity (%Heart Rate maximum) in minutes during low heart rate variability (HRV) periods (below HRV baseline consecutive days) will have a negative relationship with post-study 5K (5 kilometer) running times as measured by their activity tracker, which could lead to personalized training recommendations using HRV. This study is conducted remotely, there are no in-person visits.

Participants needed: 200
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: PepsiCo Global R&DUpdated: May 9, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Mechanisms And Prognosis of Stroke-Heart Syndrome

The incidence of stroke-heart syndrome following acute stroke, which encompasses both acute ischemic stroke and acute intracerebral hemorrhage, is notably high and is strongly associated with increased mortality and poor outcomes in stroke patients. However, the underlying mechanisms remain unclear, and there are currently no effective prevention or treatment strategies. This study aims to elucidate the neuro-humoral mechanisms of stroke-heart syndrome through multimodal imaging and multi-omics blood analysis. Additionally, it seeks to observe the progression of stroke-heart syndrome and its impact on functional outcomes, cognitive abilities, and emotional issues post-stroke. The research is expected to uncover novel blood biomarkers and brain network mechanisms associated with stroke-heart syndrome, providing potential targets and theoretical foundations for pharmacological treatments or physical interventions. Furthermore, it aims to establish a risk early-warning system for major cardiovascular complications post-stroke, enabling early identification, early intervention, and integrated brain-heart management to improve clinical outcomes for stroke patients.

Participants needed: 658
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Chensheng PanUpdated: May 1, 2025Locations: 1
Eligibility criteria

Patients admitted within 48 hours of onset, confirmed by CT/MRI as having a stro... [+1]

Previous focal brain injury (such as stroke, brain surgery, traumatic brain inju... [+6]

Status: Not yet recruiting

Heart Rate Variability and Music Listening

High anxiety levels may lead to negative outcomes, and previous studies have shown that music listening could reduce periprocedural anxiety and depression. Recent evidence suggests that a lower heart rate variability (HRV) may be associated with anxiety and depression disorders, but the association of these HRV parameters with preoperative mood in the procedural settings are less defined. In this prospective cohort pilot study, the study team will investigate the association between HRV and psychological vulnerability (anxiety, depression) in the presence of music listening before procedures. A total of 120 patients about to undergo procedures (surgery, procedures) will be recruited in three healthcare institutions in Singapore (KK Women's and Children's Hospital, Singapore General Hospital, Changi General Hospital). Patients will be asked to have their ECG readings recorded before, during, and after music listening. Preprocedural information (e.g., demographic, clinical) and psychological scores will be collected.

Participants needed: 120
Trial details
Age: 21-90Biological sex: AllType: InterventionalSponsor: KK Women's and Children's HospitalUpdated: Apr 16, 2025Locations: 3
Eligibility criteria

America Society of Anaesthesiologist (ASA) 1 to 3 adults undergoing procedures (... [+2]

With chronic pain; [+3]

Status: Recruiting

Modulation of the Inflammatory Response in Bariatric Surgery

This study will evaluate how different anesthesia techniques affect inflammation after bariatric surgery. Patients will be randomly assigned to receive one of three approaches: opioid-free anesthesia, intravenous anesthesia with opioids, or inhalational anesthesia with opioids. The study will measure blood levels of inflammation-related substances (such as IL-6, CRP, cortisol, ESR , WBC and lactate) at several time points before and after surgery. Heart rate variability will also be monitored as an indicator of the body's stress response. The results may help identify anesthesia strategies that reduce inflammation and improve recovery in patients undergoing bariatric surgery.

Participants needed: 90
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Hospital HM Nou DelfosUpdated: Apr 8, 2025Locations: 1
Eligibility criteria

Patients scheduled for bariatric surgery. [+3]

Pregnancy or breastfeeding. [+4]

Status: Not yet recruiting

Predicting Postoperative Delirium With Heart Rate Variability Obtained by Analgesia Nociception Index

The aim of this pilot study is to establish a correlation between perioperative heart rate variability (HRV) as an expression of the shift in the balance of the autonomic nervous system and the occurrence of postoperative inflammation and delirium. The main question it aims to answer is: Do patient with increased sympathetic nervous system activity develop postoperative delirium (POD) more often than patients with increased parasympathetic tone?

Participants needed: 150
Trial details
Age: 50+Biological sex: AllType: ObservationalSponsor: Medical University InnsbruckUpdated: Mar 7, 2025
Eligibility criteria

> 50 years of age [+1]

Delirium before surgery. [+19]

Status: Recruiting

Eastern Principles Acceptance and Commitment Therapy For Injury Prevention Among Nurses and Nursing Aides

This clinical trial will evaluate the effectivness of an Eastern Principles Acceptance and Commitment Therapy intervention (EPACT) relative to an estabished traditional Western-based Acceptance and Commitment Therapy intervention (ACT) and a no treatment control group. The participants for the study will be nurses and nursing aides (NNAs) who work in long-term care settings in the USA and Thailand. The primary dependent variables are work-related injuries, work stress and burnout, wellbeing, musculoskeletal symptoms, time off from work due to injury. High frequency heart rate variability will also be investigated as a predictor of responsiveness to the interventions. The study has three primary aims: 1. To compare the EPACT NNA intervention to an established traditional Western ACT NNA intervention and a no-treatment control group. 2. To identify predictors of ACT NNA and EPACT NNA responsiveness to the interventions and injury likelihood across time. 3. To assess EPACT NNA's feasibility and effectiveness across cultures. USA participants working in Ohio will be randomly assigned to one of three groups: EPACT NNA (n = 80), ACT NNA (n = 80), or a no treatment control group (n = 80). All participants will participate in an assessment session where study questnnaires are completed and a baseline high frequency HRV measurement is collected. Subsequent to the assessment, the EPACT NNA and ACT NNA participants will attend two 2.5 hour sessions spaced one week apart. The control group will have no further in-person meetings with the researchers. One-month after completing the intervention (4 weeks after the baseline assessment) a follow-up survey will be sent to participants for the first follow-up. Three months after baseline, the second follow-up survey will be sent to participants. The surveys assess demographic characteristics, organizational variables, work-related injuries, work stress, and well-being. A second RCT study will be conducted in Thailand comparing EPACT NNA (n = 40) to a no-treatment control group (n = 40) among nurses and nursing aides working in healthcare settings. The same outcome measures and procedures will be used. This research aims to develop a culturally-informed, evidence-based intervention that integrates both Western and Eastern mindfulness principles to address the high rates of work-related injuries among NNAs.

Participants needed: 255
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Bowling Green State UniversityUpdated: Feb 7, 2025Locations: 1
Eligibility criteria

USA: Employed as a nurse or nursing aide in a long-term care facility within a 1... [+3]

Status: Recruiting

Trajectory of Psychological Distress Among Infertility Women

Background: Infertility is a serious reproductive health issue and affects 48.5 million couples worldwide. Women undergoing fertility treatment often experienced psychological distress but also social stigma that is close linked to later pregnancy outcome. Despite the advancement in assisted reproductive technology, effective interventions for reducing stress, anxiety, and depressive symptoms for infertility women remain lacking. Objectives: The objective of this proposal is to evaluate the efficacy of web-based mind-body intervention combining HRV biofeedback on the infertility women's anxiety symptoms, levels of depression, HRV function, mindful awareness, infertility self-efficacy, and pregnancy rates. Methods: We plan to conduct a randomized controlled trial on the web-based mind-body intervention combining heart rate variability biofeedback. Eligible women will be recruited and randomized into three groups. Intention-to-treat analysis and mixed regression modeling will be used to estimate the effectiveness of the interventions. Anticipatory results: Effective strategies will be determined for infertility women.

Participants needed: 750
Trial details
Age: 20-60Biological sex: FemaleType: InterventionalSponsor: Taipei Medical UniversityUpdated: Jan 27, 2025Locations: 1
Eligibility criteria

20-year-old and above [+4]

Diagnosis of cardiovascular disease, depressive disorder, anxiety disorder, card... [+2]

Status: Recruiting

Effectiveness of Information Technology-Assisted Horticultural Therapy Program on Heart Rate Variability, Stress, Depression and Happiness Among Older Adults Resident in Long-Term Care Facilities

This study aims to address existing research gaps by investigating the effects of technology-assisted horticultural therapy on stress, depression, and happiness among older adults residing in long-term care facilities. By examining the modulation of the autonomic nervous system, the findings will provide a foundation for developing comprehensive health promotion programs that integrate traditional therapeutic practices with modern technology to enhance the well-being of the aging population.

Participants needed: 76
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: National Taipei University of Nursing and Health SciencesUpdated: Jan 28, 2025Locations: 1
Eligibility criteria

Agree to participate in this study [+5]

Has participated in gardening-related activities within one month of receiving t... [+4]

Status: Recruiting

Effects of Zazen Meditation in Patients With Acute Myocardial Infarction - Randomized Clinical Trial

Introduction: Coronary Artery Disease (CAD) remains the leading cause of death in Brazil, with literature indicating that in patients post-acute myocardial infarction, reduced Heart Rate Variability (HRV) has been established as a risk factor. One of the studied practices to aid in rehabilitation is meditation, believed to alter physiological aspects related to stress such as respiratory rate, oxygen consumption, carbon dioxide production, and systolic blood pressure, suggesting a better sympathetic-vagal balance. Objective: To assess the effects of Zazen meditation practice on heart rate variability in patients with recent acute and chronic myocardial infarction. Methodology: Randomized Clinical Trial. Chronic assessments will include: HRV with Polar H10 heart rate monitor, Quality of Life assessment with SF36 Quality of Life and Health questionnaire, Spiritual assessment with WHOQOL SR Spirituality, Religiosity, and Personal Beliefs questionnaire, Biochemical Parameters with ultra-sensitive PCR and cortisol, Ventricular Ejection Fraction (VEF), and 6-minute Walk Test (6MWT). Acute assessments will include: HRV with Polar H10 heart rate monitor, before and after a meditation session, in time and frequency domains. Sample size calculation was performed using Winpepi software version 11.43, with a power of 80% and significance level of 5%, determining a sample of 44 individuals. For intra-group differences analysis, ANOVA for repeated measures and/or its non-parametric counterpart, Friedman Test, will be used. For proportion analysis and comparison, Chi-square Test will be used. Expected Results: It is expected that the findings will contribute to a better understanding of the potential benefits that a meditation intervention may bring to patients who have experienced acute myocardial infarction.

Participants needed: 44
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital de Clinicas de Porto AlegreUpdated: Aug 20, 2024Locations: 1
Eligibility criteria

Recent acute myocardial infarction [+4]

Unstable angina [+7]

Status: Not yet recruiting

Helping Overcome Pressure and Exhaustion: Empowerment Classes for Southeast Asian Migrant Care Workers

As Taiwan's population ages, Southeast Asian migrant care workers are widely employed to fill the care labor gap. These workers often face symptoms of burnout and emotional stress due to long working hours and high-pressure environments. This study aims to evaluate the effects of empowerment classes on reducing burnout symptoms and emotional stress among Southeast Asian migrant care workers. The empowerment classes are designed based on expert consensus and cover three core areas: mental health and stress management, dementia care skills, and language and communication skills. The curriculum is tailored to the practical needs and cultural backgrounds of the migrant workers. A total of 120 Indonesian care workers will be randomly assigned to two groups. The first group will undergo a three-month empowerment course, while the second group will initially participate in social gatherings. Afterward, the groups will switch interventions. The study will last for 12 months, and each participant will complete seven assessments, including heart rate variability measurements and online questionnaires. The questionnaires will include the Patient Health Questionnaire-2 (PHQ-2), the Copenhagen Burnout Inventory (CBI), the Life and Cultural Adaptation Questionnaire, and the Language Proficiency Questionnaire. The study anticipates that the empowerment classes will reduce burnout symptoms and emotional stress, while enhancing cultural adaptation and language proficiency among migrant care workers.

Participants needed: 120
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: National Taiwan University HospitalUpdated: Aug 6, 2024Locations: 1
Eligibility criteria

Indonesian migrant care workers responsible for caring for patients in homes or... [+1]

Individuals unable to read the informed consent form or questionnaires in Indone...

Status: Not yet recruiting

Mindfulness-Based Self-Compassion and Vagal Nerve Stimulation on Heart Rate Variability, Psychological Resilience, and Sleep Quality

This study was conducted to determine the effects of a mindfulness-based self-compassion intervention and vagal nerve stimulation on heart rate variability, psychological resilience, and sleep quality in earthquake victims. Design: "The study was designed as a randomized experimental research, where pre- and post-intervention measurements were administered to Intervention I and Intervention II groups."

Participants needed: 26
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: İstanbul Yeni Yüzyıl ÜniversitesiUpdated: Jul 15, 2024
Eligibility criteria

Adults aged between 18 and 35, [+2]

Individuals with a psychiatric diagnosis

Status: Recruiting

Effect of Atenolol Versus Ivabradine on HRV in TRS Patients on Clozapine With Tachycardia: A Randomised Control Trial.

Clozapine is the only drug approved for Treatment Resistant Schizophrenia. However, it has been associated with many adverse drug reactions including agranulocytosis, myocarditis, sialorrhea, constipation, orthostasis, tachycardia. There are many factors that have impacted the use of clozapine in TRS patients including physician hesitation, patient denial, stopping of drug due to Adverse drug reactions. Although Tachycardia should not be the reason to stop clozapine, but data shows that it leads to discontinuation of drugs in significant patient population. If patient on clozapine develops tachycardia; first orthostasis, myocarditis and systemic infection should be ruled out. Tachycardia traditionally have been treated with B1 adrenergic blockers such as Atenolol. But the problem with beta blocker medications is that significant proportion develops hypotension. Recently developed Ivabradine slows heart rate via I(f) current, and is not associated with much cardiac adverse effects. Recent Clinical trials have been carried out to show its effects on Clozapine associated tachycardia which shows promising results. Some studies suggest using Ivabradine in patient population that have contraindication for beta blockers. Although both of these drugs are used widely in clinical practice, but as Ivabradine is relatively new drug there have been no head-to-head comparison with Atenolol. A recent meta-analysis tried to compare treatment efficacy in these patients, but found no studies that met their inclusion criteria. This current study attempts to make such comparison and guide further research.

Participants needed: 40
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: All India Institute of Medical Sciences, BhubaneswarUpdated: Jul 17, 2024Locations: 1
Eligibility criteria

Patients diagnosed with TRS (TRRIP consensus) receiving clozapine. [+3]

Already receiving Atenolol or Ivabradine. [+4]

Status: Recruiting

Compare the Effects of Different AVNS Parameters on Neck Pain, HRV, Balance in Collegiate Atheletes

This study looks at how auricular vagus nerve stimulation (AVNS) affects neck pain, heart rate variability, and balance in college athletes, additionally, if different settings of auricular vagus nerve stimulation (AVNS) affect neck pain, heart rate variability, and balance in college athletes. The participants will be split into two groups, each receiving AVNS with different settings. The study hypothesizes that vagus nerve stimulation (VNS) will reduce pain perception in college athletes. It is expected that auricular vagus nerve stimulation (AVNS) will decrease heart rate variability (HRV) in this population. Additionally, it is anticipated that college athletes undergoing AVNS will exhibit improved balance. The Investigators also believe that AVNS will decrease neck pain and enhance neck function. Finally, it is proposed that different AVNS parameters will have varying effects on pain intensity, HRV, and balance in collegiate athletes.

Participants needed: 70
Trial details
Age: 18-26Biological sex: AllType: InterventionalSponsor: University of SharjahUpdated: Jun 13, 2024Locations: 1
Eligibility criteria

Gender: Male and female Healthy collegiate athletes based in UAE [+4]

Recent injury: Had an injury within the last three months [+4]

Status: Recruiting

The ECOSTRESS Study: Influence of the Objective Structured Clinical Examination on Stress Among Medical Student

We will assess stress using heart rate variability during examination on medical student. Three time of measurement will be performed. First standardized objective clinical examination, second classic table examination and third a control day.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, Clermont-FerrandUpdated: Nov 18, 2023Locations: 2
Eligibility criteria

All medical student that agree to participate

All medical student that disagree to participate

Status: Recruiting

Effects of a Relaxation and Guided Imagery Intervention in School Context

Specific aims - To test the effects of a relaxation and guided imagery intervention with socioemotional learning content on a range of socioemotional, physiological, cognitive and academic outcomes of school-aged children, measured through self-reports, neuropsychological and physiological measures, as well as teachers and parent's reports.

Participants needed: 240
Trial details
Age: 7-12Biological sex: AllType: InterventionalSponsor: Universidade Autónoma de LisboaUpdated: Nov 7, 2023Locations: 1
Eligibility criteria

Attend the 3rd and 4th grade of the selected school (8-11 years-old)

The participant classes have benefited from the RegularMind intervention previou... [+1]

Status: Recruiting

Obesity and Bariatric Surgery According to a Biopsychosocial Perspective.

* The main goal of this prospective longitudinal observational study is to investigate the psychophysiological indicators by analyzing HRV, blood pressure, symptoms of anxiety and depression, eating behavior and quality of life during the follow-up of the general health status of patients with obesity undergoing the bariatric surgery by Roux-en-Y reconstruction reduction gastroplasty (GRYR) technique. * The main question it aims to answer is: Does bariatric surgery changes the variables studied (HRV, anxiety, depression, eating behavior, quality of life)? * Type of study: prospective longitudinal observational study * Participant population: 50 patients, both females and males, aged between 18 and 60 years, will be submitted to bariatric surgery with Roux-en-Y reconstruction reduction gastroplasty technique. Patients will be evaluated for five times: before the bariatric surgery and 3-6-12-24 months after the bariatric surgery.

Participants needed: 50
Trial details
Age: 18-60Biological sex: AllType: ObservationalSponsor: Rio de Janeiro State UniversityUpdated: Jul 18, 2023Locations: 1
Eligibility criteria

Obese and liberated patients for the bariatric surgery. [+2]

Those taking hypoglycemic medications (biguanides, sulfonylureas, glinides, acar...