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Comparing Effects of Intense Breathwork to Meditation on Altered States of Consciousness

Airways to Alteration: Investigating the Impact of Breathwork & Meditation on Conscious State

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06916312
Acronym
A2A
Enrollment
24
Registered
2025-04-08
Start date
2025-02-17
Completion date
2025-06-16
Last updated
2025-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Altered States of Consciousness, Wellbeing

Keywords

Breathwork

Brief summary

This study aims to investigate the impact of high ventilation breathwork (HVB) and meditation on altered states of consciousness (ASCs). The study will compare the effects of a single guided HVB session to a single guided body scan meditation session. The primary aim is to explore the impact of HVB and meditation on ASCs, while secondary aims relate to mental health and wellbeing.

Detailed description

The study is a randomised controlled trial (RCT) involving up to 24 healthy adult participants who have prior experience with HVB. Participants will be randomly allocated to either the HVB or meditation group. The study will assess outcomes such as altered states of consciousness, mystical experiences, emotional breakthroughs, and overall wellbeing.

Interventions

BEHAVIORALHigh ventilation breathwork

Single guided conscious connected breathing session.

BEHAVIORALMeditation

Single guided body scan meditation session.

Sponsors

DMT Quest
CollaboratorUNKNOWN
ResearchHub
CollaboratorUNKNOWN
University of Sussex
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy adults in Brighton and the surrounding area * Prior experience practising high ventilation breathwork in the form of conscious connected breathing * No history of adverse events during such prior breathwork sessions.

Exclusion criteria

* History of hypotension * Hypertension * Respiratory or cardiovascular problems * Fainting or syncope * Epilepsy or seizures * Panic disorder or panic attacks * Cerebral aneurysm * Pregnancy (and possibility one might be pregnant, trying to get pregnant, or are breastfeeding) * Breathlessness * Bradypnea * Tachypnoea * Any mental/physical issues affecting the ability to engage in breath control activities.

Design outcomes

Primary

MeasureTime frameDescription
Emotional breakthroughImmediately after the intervention.Emotional Breakthrough Inventory. Scores range from 0 to 100, with higher scores indicating greater levels of emotional breakthrough (reflecting a better outcome).
Mystical experienceImmediately after the intervention.Mystical Experience Questionnaire Brief. Comprises four subscales: transcendence, positive mood, ineffability, and mystical. Scores range from 0 to 20, with higher scores indicating a more profound mystical experience.
Altered states of consciousnessImmediately after the intervention.Five Dimensions of Altered States of Consciousness Scale. Comprises five subscales: oceanic boundlessness, dread of ego dissolution, visionary restructuralisation, auditory alterations and vigilance reduction. Scores range from 0 to 100, with higher scores indicating more profound altered states of consciousness.

Secondary

MeasureTime frameDescription
FatigueBaseline and post-intervention (one week before and after the intervention).Shortened Fatigue Questionnaire. Scores range from 4 to 28, with higher scores indicating more severe fatigue.
Mental wellbeingBaseline and post-intervention (one week before and after the intervention).Short Warwick-Edinburgh Mental Wellbeing Scale (SWEMWBS) (score range: 7 to 35; higher scores denote better outcome). Total raw scores are then transformed into metric scores using the SWEMWBS conversion table on: www.warwick.ac.uk
Depressive symptoms, anxiety, and stressBaseline and post-intervention (one week before and after the intervention).Depression Anxiety Stress Scale-21 (DASS-21) - stress, anxiety and depression subscales (score range for each: 0-21; higher scores denote worse outcomes). Score on DASS-21 then multiplied by two to convert it to the longer form DASS-42 final score.
Sleep-related impairmentBaseline and post-intervention (one week before and after the intervention).PROMIS Item Bank v. 1.0 - Sleep-Related Impairment - Short Form 4a (score range: 5-20; higher scores denote worse outcome). Data scored using a T-score transformation according to PROMIS Sleep scoring manual on: www.healthmeasures.net
Psychological insightPost-intervention (one week after the intervention).Psychological Insight Scale. Scores range from 0 to 100, with higher scores indicating greater psychological insight. An additional item separately evaluates self-reported behavioural change resulting from a psychedelic experience.
DepersonalisationImmediately after the intervention.Cambridge Depersonalisation Scale (State-Version). Scores range from 0 to 100, with higher scores indicating greater levels of dissociative symptoms.

Other

MeasureTime frameDescription
Psychedelic experience predictivenessAfter completing consent form to participate in the study.Imperial Psychedelic Predictor Scale. Scores range from 0 to 100, with higher scores donating higher predictiveness of having a psychedelic experience. Additional items assess rapport.
General experienceOne week post-intervention.Open-ended, free text.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026