ClinicalTrials.Veeva

Menu

Orgasmic Meditation and Sleep Quality

I

Institute of OM Foundation

Status

Completed

Conditions

Sleep

Treatments

Behavioral: Orgasmic Meditation

Study type

Observational

Funder types

Industry

Identifiers

NCT04455971
OMSLEEP

Details and patient eligibility

About

The primary purpose of this study is to use an observational design to examine whether the practice of orgasmic meditation (OM) is associated with app-based measures of sleep quality. A secondary purpose of this study is to examine whether the occurrence of physiological orgasm during OM practice is associated with app-based measures of sleep quality. It is hypothesized that the practice of OM will have a positive impact on sleep quality.

Enrollment

46 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. ≥18 years old, males and females, no exclusion by race, ethnicity or sexual orientation
  2. Experienced in OM practice ("experienced" defined as >10 OM sessions in lifetime)
  3. Currently practicing OM and participating in ≥1 OM session per week on average
  4. Willingness to calibrate the Sleep Cycle app and use it for 30 continuous nights
  5. Ability to charge phone by bed overnight during sleep
  6. Ability to place phone near the bed, such as on a nightstand table overnight during sleep

Exclusion criteria

  1. Inability to speak English

Trial design

46 participants in 1 patient group

OM Group
Description:
People who participate in the practice of orgasmic meditation (OM)
Treatment:
Behavioral: Orgasmic Meditation

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems