Pornography Abstinence and Nocturnal Erections in Adult Men

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age18+
SponsorEfforia, Inc

About this trial

The effects of pornography use on male sexual health remain uncertain, with mixed findings across existing literature and substantial variability at the individual level. This observational study is designed to help participants evaluate how a 30-day period of pornography abstinence affects their own sexual health and well-being, with a specific focus on nocturnal penile tumescence as a physiological biomarker.

Participants will complete a short baseline observation period during which they maintain their usual pornography consumption patterns, followed by a 30-day abstinence period. Objective nocturnal erection data will be collected using a connected wearable device, alongside validated self-report questionnaires assessing erectile function, sexual desire, mood, energy, and emotional well-being. Participants serve as their own control, allowing for within-person comparisons of outcomes before and during the abstinence period.

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Pornography Abstinence

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators