Clinical Research Directory
Browse clinical research sites, groups, and studies.
2 clinical studies listed.
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Tundra lists 2 PHYSIOLOGICAL PHENOMENA clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.
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NCT07871981
Study on Biomagnetic and Physiological Signals During Reiki Practice in Healthy Volunteers.
This study evaluates whether the practice of laying on of hands (Reiki) produces detectable biomagnetic and physiological modulations proximate to the human body in healthy volunteers. Participants are randomly assigned to one of three groups: 1. Reiki Group: Certified Reiki practitioners perform non-contact hand placement approximately 5 cm above a magnetic sensor; 2. Grounded Sham Group: Certified Reiki practitioners perform the identical protocol wearing grounded stainless steel mesh gloves designed to drain superficial electromagnetic signals; 3. Lay Control Group: Individuals without training in Reiki mimic the physical hand positions for the same duration. Researchers record magnetic signal variations near the thoracic area (xiphoid process) alongside physiological parameters before, during, and after a 15-minute intervention period to assess whether biofield effects can be objectively distinguished from simulated touch and ambient electromagnetic artifacts.
Gender: All
Ages: 18 Years - 60 Years
Updated: 2026-10-14
1 state
NCT07805044
Truway Whole-Body Digital Twin and Physiologic Resilience Study (TRU-OMNIBODY)
TRU-OMNIBODY is a prospective observational study designed to develop and independently validate a research-only whole-body digital twin. The digital twin will combine measurements from multiple body systems to create a participant-specific representation of physiologic state, resilience, and recovery. The study plans to enroll approximately 450 adults between 18 and 80 years of age. Participants will include generally healthy adults and adults with stable cardiometabolic, respiratory, or mobility-related conditions. Study measurements may include wearable-sensor data, heart rate and rhythm, blood pressure, oxygen saturation, autonomic responses, body composition, mobility, muscle function, sleep, activity, cognitive performance, point-of-care imaging, laboratory measurements, and optional biospecimens. Participants will complete a standardized resilience assessment consisting of rest, active standing, a six-minute walk, a cognitive dual task, and monitored recovery. Selected measurements will also be collected during home monitoring and follow-up visits for up to 12 months. The primary objective is to determine how accurately a locked digital-twin model predicts Whole-Body Recovery Burden, a research measure derived from the timing and magnitude of recovery across several physiologic systems. Model development and testing will be separated so that the final evaluation is performed in an independent validation cohort. This study does not assign participants to a medical treatment. Digital-twin outputs will not be used to diagnose disease, recommend treatment, or replace evaluation by a qualified health care professional.
Gender: All
Ages: 18 Years - 80 Years
Updated: 2026-09-04
1 state