Pornography Abstinence and Nocturnal Erections in Adult Men
Official title: A Real-World Observational Study Evaluating the Effects of 30 Days of Pornography Abstinence on Nocturnal Penile Tumescence, Sexual Function, and Well-Being in Adult Men
Run by Efforia, Inc · NCT07618104 · Data updated 2026-11-12
This study asks men to try 30 days of pornography abstinence and track their nighttime erections to see how their sexual health feels during this period.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | Men only |
| Enrollment | 100 (estimated) |
| Sponsor | Efforia, Inc Industry-sponsored |
| Locations | 1 site (New York, New York) |
| Status | Recruiting |
| Started | September 22, 2025 |
| Main results expected | September 22, 2026 |
| Study ends | September 22, 2026 |
| Registry record updated | June 1, 2026 |
| Trial ID | NCT07618104 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adult men who are willing to attempt pornography abstinence, comfortable using a wearable sleep device, and able to complete electronic surveys.
✕Probably not a fit
Individuals with significant sexual dysfunction requiring medical treatment or those with unstable mental health, hormonal therapy, or privacy concerns may not benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a single-arm, within-person observational study to explore whether abstaining from pornography for 30 days changes nocturnal erections and self-reported sexual function and well-being in adult men. Participants will first record baseline data while maintaining usual pornography use, then enter a 30-day abstinence period with nightly wearable measurements of nocturnal penile tumescence and weekly questionnaires. The study uses the Adam Sensor wearable and self-reported scales to capture physiological and psychosocial outcomes, without aiming to prove causality.
Why it matters
Potential benefit: If successful, findings could inform individuals about potential short-term changes in nocturnal erections and related well-being during periods of reduced pornography use.
How similar studies have gone: Prior observational work has explored behavioral changes and physiological markers with habit changes, but evidence remains mixed and exploratory in nature.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult males of legal age of consent * Willingness to attempt pornography abstinence * Ability to use a wearable device during sleep * Ability to complete electronic surveys * Willingness to purchase the study device Exclusion Criteria: * Have a history of significant sexual dysfunction requiring active medical treatment * Have current or uncontrolled mental health disorders * Have a history of addictive behaviors that may be exacerbated by abstinence * Are undergoing hormonal therapy or treatment affecting sexual function * Are experiencing unstable interpersonal or relationship stressors * Have significant concerns about privacy related to sexual health data * Have cultural or religious considerations that could cause distress
Where it's running
-
Efforia
New York, New York, United States Recruiting
Study contacts
- Study coordinator: Matthew Amsden
- Email: help@efforia.com
- Phone: (646) 679-2479
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.