Recruiting

Pornography Abstinence

Sponsor:

Efforia, Inc

Code:

NCT07618104

Conditions

Erection; Incomplete

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Accepted

Interventions

Pornography Abstinence

Study Details

Brief summary:

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.

Conditions

Erection; Incomplete

Study ID

NCT07618104

Start date

Sep 22, 2025

Status verified date

May, 2026

Completion date

Sep 22, 2026

Anticipated

Primary completion date

Sep 22, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Accepted

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

Study Design

Enrollment

100 participants

Anticipated

Interventions and Outcome Measures

Arms

Single Arm longitudinal where participants act as their own control

Single Arm longitudinal where participants act as their own control

Interventions

Pornography Abstinence

Participants will attempt to abstain from all pornography use for 30 consecutive days. Any deviations from abstinence are self-reported and logged for contextual analysis.

Primary outcome measure

  • Change in Nocturnal Penile Tumescence [ Time Frame: Baseline Day to Day 38 ]

Central Contacts and Locations

Central contacts

Locations

Efforia

Recruiting

New York, New York, United States, 10003

Contacts

More Information

Sponsor

Efforia, Inc

Last update posted

Jun 1, 2026

Last verified

May, 2026

Keywords

  • Erection
  • Men's health

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Efforia, Inc on 2026-06-01.