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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06374810
Other study ID # CCB1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 21, 2023
Est. completion date December 20, 2023

Study information

Verified date April 2024
Source California Institute of Integral Studies
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to test whether conscious connected breathwork reduces symptoms of anxiety in people with mild to severe anxiety symptoms, as measured by the Zung Self Rating Anxiety Scale. The main questions aims to answer: 1. Does conscious connected breathwork reduce symptoms of anxiety? 2. Does an increased frequency of self-practice lead to even greater reductions of anxiety symptoms. there is a comparison group: Researchers will compare whether people doing the breathwork to see if [insert effects]. Participants will participate in 1, 90 minute breath workshop per week for 6 weeks. These sessions will be held on Zoom by 2 facilitators. Participants will also be given a 10 minute recording of a guided conscious connected breathwork session that they will be encouraged to complete daily.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date December 20, 2023
Est. primary completion date December 20, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Scores of 35 or higher on the Zung self-rating anxiety scale Exclusion Criteria: - anyone having completed more than 4 sessions of Conscious Connected Breathwork - Anyone who has recently (within 1 year) started anti-depressant medication or psychotherapy - Anyone with a history of panic disorder, psychosis, angina, pregnant, seizure disorder, glaucoma

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Conscious Connected Breathwork
Participants were taught the Conscious Connected Breathwork Technique. 2 facilitators were monitoring and coaching the participants to ensure adherence to the technique
Other:
Placebo waitlist
Participants were told the study was full and that they were placed on a waiting list until the 1st cohort had completed the breathwork program

Locations

Country Name City State
United States CIIS San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
Richard Blake

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in anxiety symptoms Scores on the Zung Self Rating Anxiety Scale - Scores range from a minimum of 20 and a maximum of 80. A higher score indicates more severe symptoms of anxiety than a lower score. 6 - 8 weeks between taking the anxiety scale either before and after the breathwork program or remaining on the wait list
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