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Young Girls' Experiences of Exposure to Pornography: A Qualitative Study (ADO-X)

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.

Studieoversikt

Status

Rekruttering

Intervensjon / Behandling

Detaljert beskrivelse

  • 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.

Studietype

Observasjonsmessig

Registrering (Antatt)

30

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

Studiesteder

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen

Tar imot friske frivillige

Nei

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

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

Beskrivelse

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:

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
Girls
Teenage girls - young women aged 11-25 who have been exposed to pornography
Semi structured interview

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Qualitative content analysis of emotional experiences assessed via semi-structured interviews
Tidsramme: At the single study visit (Day 1)
Description of significant consequences experienced by female patients after viewing pornographic content: Cross coding of the verbatim
At the single study visit (Day 1)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
identify the main themes and their relationship to the patients' contexts
Tidsramme: At the single study visit (Day 1)
Analysis of the individual interviews in accordance with the principles of grounded theory
At the single study visit (Day 1)
describe the various ways in which people access pornographic content
Tidsramme: At the single study visit (Day 1)
Analysis of the individual interviews in accordance with the principles of grounded theory
At the single study visit (Day 1)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

15. april 2025

Primær fullføring (Antatt)

1. desember 2026

Studiet fullført (Antatt)

1. desember 2026

Datoer for studieregistrering

Først innsendt

12. august 2026

Først innsendt som oppfylte QC-kriteriene

4. september 2026

Først lagt ut (Faktiske)

10. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • 2024-CHITS-016

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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