Choking During Sex for Brain Function
Trial Summary
Do I have to stop taking my current medications for the trial?
The trial does not specify if you need to stop taking your current medications, but you cannot participate if you are currently taking antipsychotic medication.
What data supports the idea that Choking During Sex for Brain Function is an effective treatment?
The available research does not provide evidence that choking during sex is an effective treatment for brain function. Instead, studies focus on the prevalence and neurological effects of this behavior. For example, one study found different brain activation patterns in women who frequently experienced choking during sex, but it did not show improved brain function. Another study noted changes in brain connectivity, but again, it did not demonstrate any therapeutic benefits. Overall, the research highlights potential neurological changes but does not support the idea of choking during sex as an effective treatment.12345
What safety data exists for choking during sex as a treatment?
The existing research on choking during sex primarily focuses on its neurological and physiological effects rather than safety data. Studies have shown that frequent sexual choking is associated with different neural activation patterns and structural brain changes, such as inter-hemispheric imbalance and hyperconnectivity in certain brain regions. Additionally, surveys indicate that while many participants report pleasurable sensations, some experience negative physical responses like neck bruising and loss of consciousness. There is a lack of comprehensive safety data, and further investigation into the neurologic and health effects of this behavior is warranted.12345
Is choking during sex a promising treatment for brain function?
What is the purpose of this trial?
The purpose of this study is to examine the acute effect of being choked during partnered sex on neurological measures. The study is designed to identify the effects being choked during partnered sex on the brain through the use of neural-injury blood biomarkers, functional, diffusion, and perfusion MRI, and ocular-motor function across 3 time points (baseline, post-choking, post-non-choking). The central hypothesis is that acute neuronal structural, physiological, and functional alterations will be amplified after an incidence of choking-involved sex. The neural-injury blood biomarkers neurofilament light (NfL), glial fibrillary acidic protein (GFAP), Ubiquitin C-Terminal Hydrolase L1 (UCH-L1), and Tau will be measured in plasma, with the hypothesis that having choking involved sex will result in a increased heightened response compared to baseline and post non-choking involved sex timepoints. An additional panel of inflammatory cytokines may be considered if/when brain injury biomarkers show changes. It is also hypothesized that engaging in choking-involved sex will be associated with changes in fMRI activation patterns. White matter microstructure will be measured by diffusion imaging metrics, with the hypothesis that engaging in choking-involved sex will significantly disrupt microstructure at a post-choking involved sex time point, compared to baseline, but not at the post non-choking involved sex timepoint. The study will also assess oculomotor function as measured by near-point-of-convergence (NPC) in response to engaging in choking involved sex. The hypothesis is that NPC performance will be significantly impaired at the post choking-involved sex timepoint in comparison to both baseline and non-choking involved sex timepoints.
Eligibility Criteria
This trial is for individuals who engage in partnered sexual activity, both with and without the practice of choking. Participants must be healthy enough to undergo MRI scans and blood tests. Those with conditions affecting brain function or injury risk, such as a history of brain hypoxia or respiratory issues, may not qualify.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Baseline Data Collection
Baseline data collection including blood biomarkers, MRI, and ocular-motor function assessments
Post Choking-Involved Sex Data Collection
Data collection including blood biomarkers, MRI, and ocular-motor function assessments within 24 hours after engaging in choking-involved sex
Post Non-Choking-Involved Sex Data Collection
Data collection including blood biomarkers, MRI, and ocular-motor function assessments within 24 hours after engaging in non-choking-involved sex
Follow-up
Participants are monitored for any delayed effects or safety concerns after the main data collection phases
Treatment Details
Interventions
- Choking during Partnered Sex
Find a Clinic Near You
Who Is Running the Clinical Trial?
Indiana University
Lead Sponsor