Meditation and Yogic Breathing-driven Modulation of Neurofluid Coupling and Brain Clearance
Healthy
De qué trata este estudio
El registro no identifica actualmente este estudio como reclutando. Consulta su estado antes de planificar una evaluación.
- Tipo de estudio
- De intervención
- Fase
- No aplica
- Rango de edad
- 25 años - 60 años
- Sexo admitido
- Todos los sexos
- Voluntarios sanos
- Aceptados
- Participantes
- 120 Estimado
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Acerca de la investigación
This study will examine whether meditation and yogic breathing can alter brain fluid movement and waste clearance in healthy adults. It will also evaluate the GLYMPHOMETER, a new external forehead-worn device designed to objectively measure changes in brain fluid movement and exchange during meditation.
Leer la descripción completa
The glymphatic system is a brain waste-clearance pathway that facilitates the movement of cerebrospinal fluid (CSF) and interstitial fluid and is thought to play an important role in maintaining brain homeostasis. Emerging evidence suggests that respiration, autonomic activity, and changes in cerebral blood flow may influence CSF dynamics and related neurofluid processes. However, the effects of voluntary breathing practices and meditation on these physiological mechanisms in humans remain incompletely understood.
The SPANDHA study will investigate whether structured yogic breathing (Pranayama; specifically Nadi Shuddhi) and/or meditation (Shoonya meditation) are associated with changes in neurofluid dynamics and related physiological measures. The study will use the GLYMPHOMETER, a forehead-mounted multimodal device designed to measure physiological signals associated with neurofluid coupling during naturalistic meditation and breathing practices. The system incorporates multi-wavelength electroencephalography (EEG) and near-infrared spectroscopy (NIRS) to characterize changes in cerebral electrical activity, cerebral hemodynamics, and neurofluid-related dynamics while participants engage in the interventions.
The study will enroll approximately 100 participants, including 50 novice and 50 experienced practitioners. Using a 2-sequence crossover, participants will complete two study visits involving meditation and yogic breathing conditions. The study will evaluate changes in measures of neurofluid dynamics, cerebral compliance, autonomic regulation including heart-rate variability (HRV), and EEG-derived brain states associated with the interventions. Participants will be stratified by experience level (novice/advance) and randomized within each stratum to one of the two intervention sequences.
A subset of participants will undergo additional validation assessments using phase-contrast magnetic resonance imaging (MRI) and blood-based biomarkers. These assessments will be used to examine the relationship between measurements obtained with the GLYMPHOMETER and established measures of CSF and cerebrovascular physiology.
The primary objective of the study is to characterize the acute physiological effects of meditation and yogic breathing on neurofluid dynamics and related brain and autonomic measures. The findings may provide preliminary evidence regarding the feasibility of using voluntary breathing and meditation practices to modulate physiological processes associated with glymphatic function and may inform future studies of non-pharmacological approaches to brain health.
¿Quién podría participar?
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Inclusion Criteria:
- Healthy adults, 25-60 years old.
- Novice or Advanced as defined above.
- Fluent in English.
- Able to travel to BIDMC site for two days approximately 3-7 days apart.
Exclusion Criteria:
- History of neurological and/or neurodegenerative disorders (e.g., epilepsy, stroke, mild cognitive impairment, dementia)
- History of cardiovascular and respiratory illnesses
- History of major psychiatric disorders (e.g., schizophrenia, bipolar disorder)
- Currently diagnosed mental health issues (e.g., anxiety, depression)
- Current use of psychoactive medications, including medications prescribed for anxiety, depression, or other psychiatric conditions, or current use of stimulants or other medications that may substantially affect central nervous system function or study outcomes.
- Skin ailments, abrasions or contusions, particularly located on the forehead and face
Tratamiento, grupos y participación
El registro puede describir tratamientos y duración sin incluir un calendario completo. Pide al equipo las visitas, procedimientos, riesgos, costos y alternativas. Mantén tu atención habitual salvo que tu médico te indique un cambio.
- Asignación
- Sin asignación al azar
- Enmascaramiento
- Sin enmascaramiento
Novice Meditators
Less than 1 year of consistent meditation practice.
Behavioral: Nadi Shuddhi · Behavioral: Shoonya Meditation
Advanced Meditators
More than 5 years or a minimum of 2500 hours of consistent meditation practice
Behavioral: Nadi Shuddhi · Behavioral: Shoonya Meditation
Nadi Shuddhi BEHAVIORAL
Nadi Shuddhi is a structured yogic breathing practice involving slow, alternating respiration through the left and right nostrils in a prescribed sequence.
Shoonya Meditation BEHAVIORAL
Shoonya meditation is a structured contemplative practice characterized by conscious non-doing, in which participants maintain a relaxed, alert state while minimizing deliberate attentional selection, cognitive elaboration, and engagement with internal or external stimuli.
Qué evalúan los investigadores
Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.
Medidas principales
Acquisition of physiological data using the GLYMPHOMETER during meditation and yogic breathing sessions.
Plazo: At each study visit while the meditation is being practiced. Expected acquisition window: 20 minutes; Total number of visits: 2
Participants meeting threshold for analyzable device recordings.
Medidas secundarias
Neurofluid-related physiological measures during Shoonya meditation and Nadi Shuddhi breathing.
Plazo: At each study visit while the meditation is being practiced. Expected acquisition window: 20 minutes; Total number of visits: 2
Changes in GLYMPHOMETER-derived measures of neurofluid coupling, during Shoonya meditation and Nadi Shuddhi breathing.
(Measurement device: Glymphometer; Measure: Neurofluid coupling aka Fluid dynamics in brain)
Autonomic regulation during Shoonya meditation and Nadi Shuddhi breathing.
Plazo: At each study visit while the meditation is being practiced. Expected acquisition window: 20 minutes; Total number of visits: 2
Changes in heart-rate variability (HRV) during Shoonya meditation and Nadi Shuddhi breathing.
Very-low-frequency physiological signal characteristics
Plazo: At each study visit while the meditation is being practiced. Expected acquisition window: 20 minutes; Total number of visits: 2
Changes in predefined very-low-frequency (0.001-0.1 Hz) signal characteristics derived from GLYMPHOMETER medical™ recordings and their relationship to neurofluid-related measures.
Otras medidas
Differences in neurophysiological responses according to meditation experience.
Plazo: From date of enrollment until end of both study visits; assessed up to 4 weeks from enrollment.
Comparison of changes in GLYMPHOMETER-derived measures of neurofluid coupling between novice and advanced meditators.
Mindful Attention Awareness Scale
Plazo: Once at Baseline. Estimated acquisition window: 5-8 minutes
We assess for change in Mindfulness levels by using a validated scale for this purpose namely, Mindfulness Attention Awareness Scale (MAAS). The scale measures the individuals' ability for receptive awareness and attention to present. This aids in evaluating any change on the individual's awareness levels after the Inner engineering intervention. We compute the MAAS scores for each participant which is a mean score for 15 item questionnaires and compare the pre \& post intervention results to look for change. Participants are asked to rate on a scale of 1 (Almost Always) to 6 (Almost Never) to assess the frequency of occurrence of each experience. Mean is then computed using items from each of the 15 questions to create a MAAS score, ranging from 0 to 6. Higher MAAS scores indicate better mindfulness state.
Meditation Depth Questionnaires
Plazo: At each study visit after the meditation practice is completed. Expected acquisition window: 10-15 minutes; Total number of visits: 2
This 30-item measure assesses the subjective depth of meditation across progressively deeper experiential states. Items are typically rated on a 5-point Likert scale and are grouped into five empirically derived domains: hindrances, relaxation, personal-self/concentration, essential/transpersonal qualities, and transpersonal-self/non-duality. Together, these domains capture experiences ranging from obstacles and relaxation during meditation to focused concentration, transpersonal qualities, and experiences of diminished self-boundaries or non-dual awareness.
Correlation between GLYMPHOMETER-derived neurofluid metrics and MRI-based neurofluid dynamics (Validation of Portable Device).
Plazo: From date of enrollment until end of both study visits; assessed up to 4 weeks from enrollment.
This outcome evaluates the concurrent validity of the portable device against the gold standard. The statistical method will be a correlation analysis (Pearson or Spearman, as appropriate based on data distribution).
- Measurement 1 (Variable A): Neurofluid coupling oscillations measured via the GLYMPHOMETER medical™ device (measured as relative changes in HbO, HbR, HbT, and CSF/H2O proportional signal including interhemispheric correlation coefficient across these neurofluid compartments while gating each of them to very low frequency, respiratory and cardiac frequency bands).
- Measurement 2 (Variable B): Global neurofluid dynamics and CSF flow measured via 3T MRI using fast fMRI and phase-contrast sequences (measured as BOLD-CSF coupling magnitude and CSF stroke volume in mL).
- Assessment: The study will assess the correlation between the magnitude of oscillatory coupling in Measurement 1 with the absolute flow dynamics in Measurement 2 during the designated validation windows.
Correlation between GLYMPHOMETER-derived neurofluid metrics and plasma brain-derived biomarkers.
Plazo: From date of enrollment until end of both study visits; assessed up to 4 weeks from enrollment.
This outcome evaluates the relationship between neurofluid dynamics and blood-based markers of brain clearance. The statistical method will be a correlation analysis (Pearson or Spearman).
- Measurement 1 (Variable A): Neurofluid coupling oscillations measured via the GLYMPHOMETER medical™ device (measured as relative changes in HbO, HbR, HbT, and CSF/H2O proportional signal including interhemispheric correlation coefficient across these neurofluidic compartments while gating each of them to very low frequency, respiratory and cardiac frequency bands).
- Measurement 2 (Variable B): Plasma concentrations of brain-derived proteins/peptides (Aβ40, Aβ42, total/phosphorylated tau, NF-L, GFAP) measured via ultra-sensitive Simoa immunoassay (measured in pg/mL).
- Assessment: The study will assess the correlation between acute GLYMPHOMETER-derived neurofluid changes and plasma biomarker concentrations before and after intervention.
Qualitative assessment of meditation and breathing experiences.
Plazo: At each study visit after the meditation practice is completed. Expected acquisition window: 30 minutes; Total number of visits: 2
Qualitative characterization of participant experiences using one-on-one micro-phenomenological interviews.
Revisa las tablas completas y sus limitaciones en el registro oficial.
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1 centros
BIDMCBoston, Massachusetts, United StatesEstado desconocido
Equipo y fechas
- Patrocinador principal
- Beth Israel Deaconess Medical Center
- Inicio del estudio
- 16 nov 2026 Estimado
- Finalización primaria
- 30 nov 2027 Estimado
- Finalización del estudio
- 30 abr 2028 Estimado
- Primera publicación
- 29 oct 2026 Real
- Última actualización
- 10 nov 2026 Real
Contactos oficiales del estudio
Título oficial del estudio
Meditation and Yogic Breathing-driven Modulation of Neurofluid Coupling and Brain Clearance
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Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.
Consultado: 12 nov 2026 · Última actualización del registro: 10 nov 2026
