International Kink Health Study (IKHS)

The study design is an observational, longitudinal study with data collected online via a computer-assisted survey. Subjects will be recruited through non-probability snowball sampling.

Objectives:

  1. to document the prevalence of injuries and medical complications arising from kink activities
  2. to document how healthcare is utilized by kink-involved people
  3. to document the health outcomes particular to a large sample of kink-involved people
  4. to test whether the centrality of kink identity and degree of community belongingness affect injuries, health outcomes, and healthcare utilization

Study Overview

Status

Recruiting

Detailed Description

In 2016, TASHRA conducted the first ever health survey of the U.S. kink community, examining issues of injuries, risky behavior, health status, and healthcare access and utilization, and patient satisfaction. It included measures of kink identity centrality, coming out, and kink community involvement as predictive factors.

The findings provided a broad map of possible health disparities in a manner that was intended to direct future research. As such, several included measures did not ask any further questions to collect more detail of the context of health disparities or injuries, or their impact on the participant.

The 2016 Kink Health Survey was an anonymous online survey that collected data from kink-involved people, from April 2016 to October 2016 (six month window). 1,118 individuals completed the survey. The results indicated the following (Sprott, Randall, Smith & Woo, 2021):

  • The percentage of people who reported past experiences of kink-related injury : 13.5%
  • The percentage of people who reported delaying or avoiding healthcare because of perceived stigma: 19.0%.
  • Past negative experiences with healthcare clinicians increased the odds of delaying or avoiding care significantly, with those participants four times more likely to avoid/delay care compared to participants who did not have negative experiences.
  • A significant portion of participants had not disclosed their kink identity or behavior with their physical healthcare clinician (58.3%), nor with their therapist or mental healthcare clinician (49.6%).

The following health disparities were noted:

  • 4.1% of the sample reported being HIV positive. This is approximately 10x the national average.
  • 24% reported having attempted suicide at some point in their lives. This is approximately 5x the national average.
  • 17.98% reported having PTSD. This is 2.6x the national average.

The current proposal, the International Kink Health Survey, proposes to follow up and expand on the previous 2016 survey in the following ways:

  • to expand the collection of data beyond the United States, to other English-speaking populations
  • to clarify the timing of health status measures and health disparities in relation to the initiation of kink activities
  • to expand measures of stigma and discrimination, paying closer attention to questions of multiple minority status and intersectionality, and their relation to health status and health disparities
  • to collect more in-depth information on kink community involvement, paying attention to online activities as part of community involvement in light of the COVID-19 pandemic
  • to collect more fine-grained information about injuries or medical complications that arise from engagement in kink scenes/activities
  • To collect more fine-grained information about suicidal behavior, mental health hospitalizations, and peoples' perceptions of the role of kink in relation to these mental health challenges
  • to measure future intentions to disclose kink involvement to healthcare providers

The current proposed study will also address asexual people who engage in kink/BDSM behaviors (bondage, sadomasochism, and power exchange). The 2016 Kink Health Survey included this sexual orientation group, and we will continue to address this group.

The study design is an observational, longitudinal study with data collected online via a computer-assisted survey. Subjects will be recruited through non-probability snowball sampling. Interested individuals will initially be screened for inclusion criteria. All completed questionnaires will be reviewed to ascertain whether inclusion criteria are met or exclusion criteria are met. Those who meet the inclusion criteria will be sent a message asking them to read and sign the Informed Consent form if they wish to enroll in the study. Those who meet the exclusion criteria or who do not complete an Informed Consent form after 3 contacts will have their information on the screening questionnaire in Ripple de-identified. In order to characterize the prescreening sample for reporting purposes, the de-identified data will be retained and may be analyzed. If they provide their consent, prospective participants will be considered enrolled in the study and will be sent email invitations to fill out survey instrument 1, and then every week sent an email to fill out survey instrument 2, and so on, as appropriate.

IKHS Survey Instrument 1:

Demographics Kink Behaviors Kink Fantasies Kink/Sexual Desire

IKHS Survey Instrument 2:

Future Disclosure COVID

IKHS Survey Instrument 3:

Kink Injury

IKHS Survey Instrument 4:

Physical Health

IKHS Survey Instrument 5:

Mental Health

IKHS Survey Instrument 6:

Healthcare Utilization

IKHS Survey Instrument 7:

Sex Work Consent Violations Kink and Past Trauma Stigma Family Support Sexual Shame and Pride Scale

IKHS Survey Instrument 8:

Adverse Childhood Events / Sensation-Seeking Alcohol / Drug

Study Type

Observational

Enrollment (Anticipated)

3164

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: Anna M Randall, LCSW
  • Phone Number: 650-888-9640‬
  • Email: anna@tashra.org

Study Locations

    • California
      • Rio Vista, California, United States, 94571
        • Recruiting
        • TASHRA
        • Contact:
        • Principal Investigator:
          • Richard A Sprott, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

People involved in kink activities: power exchange (Dominant/submissive roles), bondage, sadomasochism, or fetish activities.

Description

Inclusion Criteria:

  1. Successful completion of screening checklist to indicate one of the following conditions:

    1. recurring, long-standing fantasies that focus on kink, in areas such as: power exchange (Dominant/submissive roles), bondage, sadomasochism, or fetish activities. By fetish, we mean a type of sexual desire in which gratification depends on or is significantly increased by particular objects, clothing items, parts of the body, or types of persons.
    2. OR currently engaging, or have engaged in the past, in consensual kink activities such as power exchange (Dominant/submissive roles), bondage, sadomasochism, or fetish activities.
  2. Age of majority in the legal jurisdiction (geographic location) where the survey is taken (usually age 18)
  3. English-language proficiency sufficient to understand the study instruments
  4. Completion of an electronically signed and dated informed consent form

Exclusion Criteria:

People who respond "no" to the following question on the screening checklist

  • I am familiar with the importance of consent and I endorse negotiation and safe words or safe signals in my sexual or kink play
  • Clearly fraudulent use of the internet survey, such as: evidence of non-human data entry via an internet "bot", duplicative or prank data entry that entails contradictory or clearly fraudulent data.
  • Any condition that, in the professional judgement of the Principal Investigator, should exclude an individual from participation in the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
2022 Cohort
  1. Successful completion of screening checklist to indicate one of the following conditions:

    1. recurring, long-standing fantasies that focus on kink, in areas such as: power exchange (Dominant/submissive roles), bondage, sadomasochism, or fetish activities. By fetish, we mean a type of sexual desire in which gratification depends on or is significantly increased by particular objects, clothing items, parts of the body, or types of persons.
    2. OR currently engaging, or have engaged in the past, in consensual kink activities such as power exchange (Dominant/submissive roles), bondage, sadomasochism, or fetish activities.
  2. Age of majority in the legal jurisdiction (geographic location) where the survey is taken (usually age 18)
  3. English-language proficiency sufficient to understand the study instruments
  4. Completion of an electronically signed and dated informed consent form

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Kink Injury
Time Frame: Year 1
self-report of injury or medical complication while engaged in kink activities; type of injury; frequency of injury
Year 1
Healthcare Utilization
Time Frame: Year 1
self-report of: types of care; frequency of care; patient satisfaction; experiences of discrimination in healthcare interactions
Year 1
Health Disparities
Time Frame: Year 1
self-report of: mental health issues; suicidality; obesity; sexually transmitted infections; blood-borne pathogens; alcohol/drug use
Year 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Community Belongingness
Time Frame: Year 1
self-report of sense of belonging to a kink community
Year 1
Centrality of Kink Identity
Time Frame: Year 1
self-report of felt centrality of kink identity to sense of self
Year 1
Concealment / Disclosure of Kink Involvement
Time Frame: Year 1
self-report of behavior on disclosure of kink identity or kink involvement
Year 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Richard A Sprott, PhD, The Alternative Sexualities Health Research Alliance

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 1, 2022

Primary Completion (Anticipated)

July 31, 2023

Study Completion (Anticipated)

July 31, 2028

Study Registration Dates

First Submitted

January 15, 2022

First Submitted That Met QC Criteria

March 31, 2022

First Posted (Actual)

April 8, 2022

Study Record Updates

Last Update Posted (Actual)

October 21, 2022

Last Update Submitted That Met QC Criteria

October 19, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • T2021-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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