ClinicalTrials.gg
RecruitingNCT07812662ADO-XUpdated Sep 10, 2026

Young Girls' Experiences of Exposure to Pornography: A Qualitative Study

An observational study in Exposure to Pornography, sponsored by Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer. Recruiting at 1 site in France. Open to female participants aged 11 Years to 25 Years. Per ClinicalTrials.gov, last updated 2026-09-10.

Sponsored by Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer · Observational

From the registry’s dates

  • Started Apr 2025; still recruiting 1 year 6 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
30
Ages
11 Years to 25 Years
Sex
Female
01

Study summary

This qualitative study aims to explore the experiences, meanings, and uses of pornography among female adolescents and young women receiving care in child and adolescent psychiatry services. Participants aged 12 to 25 years will be recruited from inpatient and outpatient settings. Exclusion criteria will include an acute psychotic episode or an acute mood episode that could compromise participation in an interview.

Using semi-structured interviews, the study will examine the circumstances and age of first exposure to pornography; participants' emotional responses and evolving perceptions; subsequent patterns of viewing, use, avoidance, or sharing; and the roles pornography may play in their lives. Particular attention will be paid to its possible functions in relation to curiosity, sexual learning, arousal, identity exploration, peer relationships, emotional regulation, coercion, or distress.

The interviews will also explore how participants perceive the place of pornography in their relational and sexual trajectories, including its potential influence on expectations, consent, body image, sexual practices, intimate relationships, and current sexual life. Rather than assuming that pornography has uniformly harmful or beneficial effects, the study will seek to understand its diverse, ambivalent, and context-dependent meanings.

Finally, participants will be invited to formulate recommendations concerning public policy, pornography regulation, prevention, and sexuality education. By centring the perspectives of young female psychiatric service users, this study aims to contribute to a more nuanced understanding of pornography within contemporary adolescent development and clinical care.

Read the detailed description
  • This study will use a qualitative design informed by Grounded Theory methodology.
  • Data will be collected through individual semi-structured interviews, lasting approximately 30 to 60 minutes. Interviews will be audio-recorded and transcribed verbatim.
  • Data collection and analysis will proceed iteratively. The interview guide may be refined during the study in response to emerging findings. Transcripts will be independently coded by three investigators. Coding discrepancies will be discussed collectively in order to develop a shared coding framework and strengthen the credibility of the analysis.
  • Analysis will follow a constant comparative approach, comparing accounts within and across participants in order to identify recurring themes, divergent experiences, and emerging conceptual categories. Particular attention will be paid to participants' own meanings, language, and interpretations of pornography in their personal, relational, and sexual trajectories. The analysis will aim to develop an interpretative account of the different ways pornography may be encountered, used, negotiated, or experienced by female adolescents and young women receiving psychiatric care.
02

Conditions studied

  • Exposure to Pornography

Browse trials for

Keywords

  • Pornography
  • Trauma
  • Child developpement
  • Sexual abuse
03

In context

Wounds and Injuries

2,217 studies on the registry are indexed under Wounds and Injuries; 441 are open to participants now.

This study's planned enrollment of 30 is below the median of 169 across 690 observational studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer is the lead sponsor of 78 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
11 Years to 25 Years
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Girls aged 11 to 25 years who are being treated in the Child and Adolescent Psychiatry Department at CHITS or the follow-up clinic

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Girls aged 11 to 25 years who are being treated in the Child and Adolescent Psychiatry Department at CHITS or the follow-up clinic
  • Patient, or legal guardians if a minor, who does not object to the research;
  • Patient who engages in the consumption of pornographic content.

Exclusion criteria

Exclusion Criteria:

  • intellectual deficit
  • psychosis
  • acute mood episode
  • pregnant or breastfeeding
  • Patient under judicial protection
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
30 participants (estimated)
Patient registry
No

Groups and cohorts

  • Girls

    Teenage girls - young women aged 11-25 who have been exposed to pornography

    Other: Semi structured interview

Interventions

  • OtherSemi structured interview

    Semi structured interview

06

What researchers measure

Primary outcomes

  1. Qualitative content analysis of emotional experiences assessed via semi-structured interviews

    Description of significant consequences experienced by female patients after viewing pornographic content: Cross coding of the verbatim

    Time frame: At the single study visit (Day 1)

Secondary outcomes

  1. identify the main themes and their relationship to the patients' contexts

    Analysis of the individual interviews in accordance with the principles of grounded theory

    Time frame: At the single study visit (Day 1)

  2. describe the various ways in which people access pornographic content

    Analysis of the individual interviews in accordance with the principles of grounded theory

    Time frame: At the single study visit (Day 1)

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2025 (actual). Primary completion is estimated for Dec 2026, 20 months after the start.

Of 265 non-industry observational studies under Wounds and Injuries, half reached primary completion within 28 months of starting (the median), counting those still running; a quarter within 12 and three quarters within 60. This study's planned 20 months is below that.

Counting every sponsor, half of 312 studies reached it within 28 months; a quarter within 12 and three quarters within 60.

Wounds and Injuries covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 12, 2026
First posted
Sep 10, 2026
StartActual
Apr 15, 2025
Primary completionEst.
Dec 2026
CompletionEst.
Dec 2026
Last update
Sep 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07812662
Lead sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Responsible party
Sponsor
First posted
Sep 10, 2026
Start date
Apr 15, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Sep 10, 2026

Study contacts

Nadège BOURVIS, MD, PhD
Contact
nadege.bourvis@ch-toulon.fr
+33 628 22 35 21 ext. +33
Asmaa JOBIC, PhD
Contact
asmaa.jobic@ch-toulon.fr
+33483772061 ext. +33

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion