Clinical Trials Directory

Trials / Completed

CompletedNCT05577377

OM and Trauma Study

An Unblinded, Uncontrolled, 1-month Interventional Single Group Pilot Study, to Assess the Possibility of Orgasmic Meditation Practice Being Used as a Possible Intervention for PTSD.

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
28 (actual)
Sponsor
Institute of OM Foundation · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The primary purpose of this study is to use an unblinded, uncontrolled, 1-month interventional single group pilot study, to assess the possibility of Orgasmic Meditation practice being used as a possible intervention for PTSD. The secondary purpose of this study is to examine if OM is associated with a decrease in the symptoms and self-assessed experiences associated with trauma. The OM Trauma Protocol (OMTP) is designed to systematize the application of Orgasmic Meditation (OM) for individuals seeking relief from a wide variety of problems and/or help them in their pursuit of eudaimonia. The study protocol will evaluate whether OMing (the act of practicing OM) shows potential for being an effective intervention for people suffering from Post-Traumatic Stress Disorder (PTSD).

Conditions

Interventions

TypeNameDescription
BEHAVIORALOrgasmic MeditationOrgasmic Meditation (OM) is a structured attention training practice that you do with another person by following a predefined set of detailed instructions. One of the two people participating in the OM must have a clitoris. In this partnered practice, one person strokes the clitoris of another person with the tip of their left index finger for 15 minutes.

Timeline

Start date
2022-03-23
Primary completion
2024-04-18
Completion
2024-08-25
First posted
2022-10-13
Last updated
2024-09-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05577377. Inclusion in this directory is not an endorsement.