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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05219825
Other study ID # 8165
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 6, 2022
Est. completion date August 2024

Study information

Verified date February 2024
Source New York State Psychiatric Institute
Contact Danielle Mayall, B.A
Phone (888) 497-8427
Email danielle.mayall@nyspi.columbia.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this proof-of-concept study is to evaluate the safety, feasibility and acceptability of a breathwork workshop intervention in individuals with cannabis use disorder.


Description:

This study will test a 1-week breathwork workshop for treatment-seeking adults with a diagnosis of cannabis use disorder. The intervention consists of an enhanced breathing session with evocative music to facilitate experiencing non-ordinary states of consciousness, in addition to brief therapeutic interventions based on Motivational Interviewing and Mindfulness-based Relapse Prevention (MBRP). The primary aim is to test the acceptability, feasibility and safety of enhanced breathwork in a therapeutic framework for cannabis use disorder. In addition, the investigators seek to understand the phenomenology of breathwork that may explain any change related to addictive behaviors, as well as biological changes that occur during the breathwork session through heart rate variability and electroencephalography.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date August 2024
Est. primary completion date August 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - 18-70 years of age - Meets Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria for active cannabis use disorder. - Seeking treatment for their cannabis use Exclusion Criteria: - Meets DSM-V criteria for schizophrenia or any psychotic illness or any dissociative disorder (Dissociative identity disorder, Dissociative amnesia, Depersonalization/derealization disorder). - Active substance use disorder except for cannabis, nicotine, and caffeine. - History of severe withdrawal symptoms (i.e withdrawal seizures). - History of dementia, epilepsy or seizures, cardiac arrhythmia, pacemaker/defibrillator, heart failure, asthma, panic disorder and other respiratory illnesses (ie: COPD).

Study Design


Intervention

Behavioral:
Breathwork workshop
Participants will complete 1.5 hours of breathwork session in addition to a total of 6 hours of brief psychotherapeutic intervention in a span of 1 week. The therapy sessions will occur both before and after the breathing session.

Locations

Country Name City State
United States New York State Psychiatric Institute New York New York

Sponsors (1)

Lead Sponsor Collaborator
Elias Dakwar

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability of the breathwork session Acceptability of the breathwork intervention through self-reported questionnaires. One week after the breathing session.
Primary Safety of the breathing session Occurrence of adverse effects through a self-reported questionnaire. 24 hours after the breathing session.
Secondary Change in Cue Reactivity Serial visual analogue scale for craving elicited by cannabis use. From baseline to 1 month after the breathing session.
Secondary Change in Motivation to Quit Measured with the "Stages of Change Readiness and Treatment Eagerness Scale." From baseline to 1 month after the breathing session.
Secondary Change in cannabis use Changes in cannabis use as measured by the Timeline Followback. From baseline to 1 month after the breathing session.
Secondary Phenomenology of breathwork #1 Subjective experiences during the breathing session will be assessed with the 30-item Mystical Experience Questionnaire. 24 hours after the breathing session
Secondary Phenomenology of breathwork #2 Subjective experiences during the breathing session will be assessed with the Emotional Breakthrough Inventory. Obtained 24 hours after the breathing session
Secondary Heart Rate Variability Polar (H10) chest strap Measured during breathing session
Secondary Electroencephalographic changes Electroencephalograpy cap Measured during breathing session
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