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Pornography Abstinence and Nocturnal Erections in Adult Men

2026年5月26日 更新者:Efforia, Inc

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

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.

研究概览

地位

招聘中

详细说明

This single-arm, real-world observational study evaluates the association between pornography abstinence and changes in nocturnal penile tumescence, sexual function, and psychosocial outcomes in adult men.

During an initial baseline phase, participants continue their typical pornography use while collecting objective nocturnal erection data and completing baseline questionnaires. Participants then enter a 30-day abstinence period, during which they attempt to refrain from pornography use. Abstinence adherence is self-reported, with lapses logged as observational data rather than protocol violations.

Nocturnal penile tumescence is assessed nightly using the Adam Sensor, a non-invasive wearable device that measures changes in penile circumference during sleep. Additional outcomes are assessed using validated questionnaires administered at baseline and at weekly intervals. The study is exploratory and signal-detecting in nature and is not designed to establish causality.

Study Design

Study Type: Observational

Study Design: Single-arm, within-participant comparison

Time Perspective: Prospective

Masking: None (Open Label)

Primary Purpose: Health outcomes assessment / signal detection

Additional information can be found at the study recruitment landing page here: https://app.efforia.com/30-day-tv-abstinence-challenge/

研究类型

观察性的

注册 (估计的)

100

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

  • 姓名:Matthew Amsden
  • 电话号码:(646) 679-2479
  • 邮箱:help@efforia.com

学习地点

    • New York
      • New York、New York、美国、10003
        • 招聘中
        • Efforia
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

取样方法

非概率样本

研究人群

Adult men who are interested in evaluating how a 30-day period of pornography abstinence may affect their sexual health, nocturnal erections, and overall well-being. Participants are self-selected volunteers who report current or recent pornography use, are able to attempt abstinence for the duration of the study, and are willing to use a non-invasive wearable device to collect nocturnal penile tumescence data and complete electronic questionnaires. The study population reflects a real-world, consumer-based sample rather than a clinically diagnosed population.

描述

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

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
Single Arm longitudinal where participants act as their own control
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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Nocturnal Penile Tumescence
大体时间:Baseline Day to Day 38

Measure: Adam Sensor - Nocturnal Erection Tracking

Description:

Objective measurement of nocturnal penile tumescence, Frequency/Time nocturnal erections per night

Baseline Day to Day 38

次要结果测量

结果测量
措施说明
大体时间
Change in Erectile Function
大体时间:Baseline to Day 38 after intervention

Measure: International Index of Erectile Function (IIEF-15)

Scale Range: 5-75 (higher scores indicate better erectile and sexual function)

Description:

Assesses erectile function, orgasmic function, sexual desire, intercourse satisfaction, and overall satisfaction.

Baseline to Day 38 after intervention
Change in Sexual Desire
大体时间:Baseline to Day 38 after intervention

Measure: Sexual Desire Inventory-2 (SDI-2)

Scale Range: 0-112 (higher scores indicate greater sexual desire)

Description:

Measures both dyadic and solitary sexual desire.

Baseline to Day 38 after intervention
Change in Pornography Consumption Patterns
大体时间:Baseline to Day 38 after intervention

Measure: Weekly Pornography Consumption Survey (custom self-report)

Scale: Frequency and duration categories (ordinal)

Description:

Tracks self-reported pornography use and abstinence adherence.

Baseline to Day 38 after intervention
Change in Mood, Energy, and Emotional Well-Being
大体时间:Baseline to Day 38 after intervention

Measure: Weekly Self-Assessment Check-In (custom)

Scale: 1-10 Likert-type scales (higher scores indicate more favorable states)

Description:

Assesses perceived mood, mental clarity, energy level, and emotional resilience.

Baseline to Day 38 after intervention

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2025年9月22日

初级完成 (估计的)

2026年9月22日

研究完成 (估计的)

2026年9月22日

研究注册日期

首次提交

2026年2月24日

首先提交符合 QC 标准的

2026年5月26日

首次发布 (实际的)

2026年6月1日

研究记录更新

最后更新发布 (实际的)

2026年6月1日

上次提交的符合 QC 标准的更新

2026年5月26日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • 38321

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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