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Strategier for implementering af globalt samtykke for at forhindre seksuel vold hos universitetsmænd (SCALE)

22. juli 2026 opdateret af: Kathryn Yount, Emory University

SKALA: Strategier til implementering af globalt samtykke til forebyggelse af seksuel vold hos universitetsmænd

Dette projekt, SCALE, vil være det første til at sammenligne implementeringsstrategier med lavere intensitet (standard) og højere intensitet for at levere GlobalConsent - et effektivt webbaseret program til forebyggelse af seksuel vold - til mænd, der går på seks universiteter i hele Vietnam. Efter et stringent, blandet-metoder, komparativt afbrudt-tids-serie design, vil forskere indsamle nye data for at sammenligne implementeringssikkerhed, drivere og resultater, effektivitet og omkostningseffektivitet på tværs af implementeringsstrategigrupper. Dette partnerskab omfatter universiteter, der også er engageret i et voldsforebyggende uddannelsesstipendium (D43TW012188), der tilbyder en uovertruffen mulighed for kapacitetsstyrkelse og evidensgenerering for at vejlede nationale ledere om de bedste strategier til at lancere GlobalConsent i stor skala, for at adressere en kønsbestemt risikofaktor i teenageårene, og derved forbedre en række sundhedsresultater ind i voksenlivet.

Studieoversigt

Detaljeret beskrivelse

Seksuel vold er udbredt i teenageårene og øger risikoen for skadelige langsigtede helbredseffekter. Seksuel vold omfatter enhver seksuel handling begået mod en person uden frit givet samtykke. Alle køn kan opleve seksuel vold, men seksuel vold belaster kvinder oftere end mænd globalt, og mænd udøver oftest sådan vold. Ungdomsalderen er en periode med sårbarhed over for seksuel vold, hvor omkring hver femte universitetskvinde i USA oplever et seksuelt overgreb på campus, og 91 % af ofrene er kvinder. Mindre er kendt om antallet af seksuel vold på universitetscampusser. Alligevel bekræfter estimater fra store undersøgelser i flere lande, at unge mænds rapporterede seksuelt voldelige adfærd og unge kvinders rapporterede ofre for seksuel vold er høj, også i Asien/Stillehavet. I Vietnam, fra 2010 til 2019, steg kvinders indberetninger om livslang seksuel vold begået af en partner (10 % til 13 %), især hos kvinder 18-24 år (5 % til 14 %). Sådanne tendenser kan afspejle ændret eksponering og større åbenhed for at diskutere sex og seksuel vold. Næsten hver tiende kvinde (9 %) rapporterer også om seksuel vold uden partner siden 15-årsalderen, for det meste begået af ikke-familiens mandlige bekendte, kolleger eller fremmede. Unge kvinder, der er ofre for seksuel vold, har øget risiko for akutte og kroniske psykiske og fysiske helbredstilstande.

Forskerne vil bruge RE-AIM (Reach, Effectiveness, Adoption, Implementation og Maintenance) og Proctor et al. rammer og et komparativt afbrudt tidsseriedesign (CITS) med blandede metoder til at sammenligne implementering; implementeringsdrivere og resultater; implementeringseffektivitet; og omkostningseffektiviteten af ​​implementeringsstrategier med lavere intensitet vs. højere intensitet (LIS; HIS) for at levere GlobalConsent.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

3439

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

      • Can Tho, Vietnam
        • Rekruttering
        • Can Tho University of Medicine and Pharmacy (CTUMP)
      • Da Nang, Vietnam
        • Rekruttering
        • Da Nang University of Medical Technology & Pharmacy (DUMTP)
      • Haiphong, Vietnam
        • Rekruttering
        • Hai Phong University of Medicine and Pharmacy
      • Hanoi, Vietnam, 116001
        • Rekruttering
        • Hanoi Medical University
        • Kontakt:
          • Tran Hung Minh, MD, MSc
          • Telefonnummer: 0243 5770261
      • Ho Chi Minh City, Vietnam
        • Rekruttering
        • Ho Chi Minh City Medicine and Pharmacy University
      • Ho Chi Minh City, Vietnam
        • Rekruttering
        • Hong Bang University
      • Huế, Vietnam, 470000
        • Rekruttering
        • Hue University of Medicine and Pharmacy

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inklusionskriterier for studerende:

  • 18-24 år,
  • Mænd, der identificerer sig som heteroseksuelle eller biseksuelle (som er tiltrukket af kvinder),
  • Indskrevet som førsteårsstuderende på et af de seks deltagende studieuniversiteter i Nord-, Central- og Sydvietnam.

Eksklusionskriterier for studerende:

  • Voksne kan ikke give samtykke
  • Personer, der endnu ikke er voksne (spædbørn, børn, teenagere)

Inklusionskriterier for fakultetet:

  • Alle tilmeldte undervisere på hvert af de seks deltagende studieuniversiteter vil være berettiget til at deltage i klimaundersøgelserne i år 1, 3 og 5.

Eksklusionskriterier for fakultetet:

  • Ingen

Inklusionskriterier for ledere:

  • Anbefaling af studiepersonale på hvert deltagende studieuniversitet
  • Viden om implementeringsmiljøet og implementering af GlobalConsent.

Eksklusionskriterier for ledere:

  • Ingen

Inklusionskriterier for implementeringsteams:

  • Identificeret af relevant undersøgelsespersonale.

Ekskluderingskriterier for implementeringsteams:

  • Ingen

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Studerende
Studerende i begge randomiseringsgrupper bliver aktive forbrugere af GlobalConsent med en e-mailintroduktion til programmet, proces, leveringsplan, dataindsamlingsprocedurer og samtykke.
Studerende i LIS-gruppen vil modtage grundlæggende implementeringsstrategier af GlobalConsent, der ofte bruges til at levere online-programmer på amerikanske universiteter med påmindelser om færdiggørelse af e-mail/SMS med en forudbestemt frekvens i 12 uger.
Andre navne:
  • LIS-Studerende
Students in the HIS group will receive educational outreach in a pre-implementation orientation to GlobalConsent, covering similar topics and three monthly one-hour learning sessions during implementation in which technical questions about program access or progression can be addressed; more intensive intervention to enhance adherence with more frequent email/Short Message Service (SMS), completion reminders; and demand generation encouraging program completion.
Andre navne:
  • HANS-Elever
Eksperimentel: Fakultet
Fakultetet vil modtage adgang til undervisningsmateriale baseret på universitetets randomiseringsimplementeringsstrategigruppe.
  • Passiv adgang til webbaseret undervisningsmateriale
  • Rådhuse (3) med generelle fakulteter til at definere seksuel vold; rater hos unge; akutte/kroniske effekter i løbet af livsforløbet; primære forebyggelse evidensbaserede interventioner (EBI'er)
Andre navne:
  • HANS-Fakultetet
Passiv adgang til webbaseret undervisningsmateriale
Andre navne:
  • LIS-Fakultet
Eksperimentel: Ledere
Ledere vil modtage stedspecifikke (universitet) invitationer og materiale baseret på implementeringsstrategigruppen.
  • Stedspecifik invitation til at deltage
  • Passiv adgang til webbaseret undervisningsmateriale
  • Et pre-implementation webinar til at definere seksuel vold; rater blandt unge i Vietnam; akutte/kroniske effekter over livsforløbet; primære forebyggelse EBI'er; opsummering af projektbeskrivelse og samarbejde; del GlobalConsent-webstedet for passiv adgang til undervisningsmateriale
  • Månedlige e-mails fra uddannede interne facilitatorer til universitetsledere med opdateringer om implementeringsfremskridt
  • Et webinar efter implementering til at dele anonymiserede resultater (af IS-gruppe); diskutere plan for opretholdelse (herunder vejledning i, hvordan man håndterer indberetning af seksuel vold i eksisterende universitetsrådgivningscentre)
Andre navne:
  • HIS-ledere
  • Stedspecifik invitation til at deltage
  • Passiv adgang til webbaseret undervisningsmateriale
  • Et pre-implementation webinar til at definere seksuel vold; rater blandt unge i Vietnam; akutte/kroniske effekter over livsforløbet; primære forebyggelse EBI'er; opsummering af projektbeskrivelse og samarbejde; del GlobalConsent-webstedet for passiv adgang til undervisningsmateriale
Andre navne:
  • LIS-ledere
Eksperimentel: Medlemmer af implementeringsteam
Medlemmer af implementeringsteamet vil modtage passiv adgang til webbaseret materiale og træning i henhold til den universitetsspecifikke implementeringsstrategigruppe.
  • Passiv adgang til webbaseret undervisningsmateriale
  • Personlig teknisk træning på campus-dækkende implementering af GlobalConsent; diskussion og demonstration af GlobalConsent-programmet; standardiseret implementeringsmanual
  • Personlig lederuddannelse for at forkæmpe GlobalConsent med interne interessenter (ledere, implementeringsteams, fakultet, studerende); ledelsesstile; ledelse af teams; indflydelse uden autoritet; håndtering af konflikter; følelsesmæssig intelligens; forhandling; lede forandring
  • Hver anden uge (seks) 1-times optagede kvalitetsforbedringsteamwebinarer for at give genopfriskningstræning; vurdere implementeringsfremskridt; vurdere ændringer; opbygge peer-netværk; give anonymiserede data om implementeringsfremskridt til diskussion
Andre navne:
  • HIS-Implementeringsteammedlemmer
  • Passiv adgang til webbaseret undervisningsmateriale
  • Personlig teknisk træning på campus-dækkende implementering af GlobalConsent; diskussion og demonstration af GlobalConsent-programmet; standardiseret implementeringsmanual
Andre navne:
  • Medlemmer af LIS Implementeringsteam

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Students' Reported Prosocial Bystander Behavior
Tidsramme: Baseline (month 10), every 6 months up to 30 months
Students will be asked if they had engaged in any of seven prosocial bystander behaviors in the past 3 months (or since the last time completing the questionnaire). Items are scored as 0 = never performed, 1 = performed once, 2 = performed more than once. The numbers of participants who report engaging in at least one of seven prosocial bystander behaviors at least once are presented here.
Baseline (month 10), every 6 months up to 30 months
Students' reported Sexually Violent Behavior
Tidsramme: Baseline (month 10), every 6 months up to 30 months
The Sexual Experiences Survey (SES) is an assessment tool used to measure the prevalence of sexual aggression. It is designed to measure the frequency and severity of sexual aggression acts committed by an individual. The SES is a self-report questionnaire developed by researchers at the University of Michigan. The Sexual Experiences Survey - Short Form Victimization is a multi-item measure to assess unwanted sexual victimization. Surveys will be provided every six months for up to 30 months.
Baseline (month 10), every 6 months up to 30 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Handicapvurdering og tidsplan
Tidsramme: Baseline

Kun studerende: Handicapvurderingen vil blive vurderet ved at bruge World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0), som er et generisk vurderingsinstrument for sundhed og handicap, der bruges på tværs af alle sygdomme, herunder psykiske, neurologiske og vanedannende lidelser, der gælder i både kliniske og generelle befolkningsindstillinger. Det er et værktøj til at måle niveauet af handicap og funktion på seks domæner. Svarene bedømmer hvert spørgsmål på en skala fra 0 (ingen) til 4 (ekstremt eller kan ikke).

Der er tre scoringsmetoder: simpel score, kompleks score eller gennemsnitlig score. Den simple score er summen af ​​vurderingerne for hvert spørgsmål. Den komplekse score er summen af ​​vurderingerne ganget med en vægtfaktor. Den gennemsnitlige score er gennemsnittet af vurderingerne for hvert domæne.

Baseline
Diagnostisk og statistisk manual (DSM)-5 Måling af krydsskæringssymptom
Tidsramme: Baseline
Kun studerende: DSM-5 Self-Rated Level 1 Cross-Cutting Symptom Measure-Adult er et værktøj designet til at vurdere mentale sundhedsdomæner, der er vigtige på tværs af forskellige psykiatriske diagnoser. Den består af 23 spørgsmål, der evaluerer 13 psykiatriske domæner, såsom depression, angst, somatiske symptomer og meget mere. Hvert punkt på målingen er vurderet på en 5-punkts skala (0=ingen eller slet ikke; 1=let eller sjælden, mindre end en dag eller to; 2=mild eller flere dage; 3=moderat eller mere end halvdelen af dage; og 4 = alvorlig eller næsten hver dag). En mild (dvs. 2) eller højere vurdering af ethvert element inden for et domæne kan vejlede yderligere forespørgsler og opfølgning for at afgøre, om en mere detaljeret vurdering for det pågældende domæne er nødvendig. Konsekvent høje scores på et bestemt domæne kan indikere signifikante og problematiske symptomer for individet, som kan berettige yderligere vurdering, behandling og opfølgning
Baseline
Alkoholnedsættelse Viden/virkninger af alkohol på kognition
Tidsramme: Baseline, hver 6. måned i op til 30 måneder.
Kun studerende: Denne formular beder respondenternes aftale eller uenighed om 5 alkoholrelaterede spørgsmål med fokus på beslutningstagning, adfærd og seksuel vold. Den vurderer aftale eller uenighed ved hjælp af en 5-punkts Likert, der spænder fra "helt uenig" til "helt enig".
Baseline, hver 6. måned i op til 30 måneder.
Perceptions of Sexual Violence form at their respective university
Tidsramme: Baseline (month 10) and up to 49 months

Perceptions of sexual violence will be assessed by respondents' rating their level of agreement with 3 statements regarding the frequency and impact of sexual violence at their university using a 5-point Likert scale ranging from "Totally disagree" to "Totally agree."

Surveys will be provided to all groups at different time points as follows:

  • Students: Baseline (month 10), every 6 months up to 30 months
  • Faculty: Baseline, 32 months, and 44 months
  • Leaders: Baseline and 41 months
  • Implementation Team: Baseline, month 25, month 29, and month 32
Baseline (month 10) and up to 49 months
Implementation Team Scale for staff and supervisors
Tidsramme: Baseline, month 25, month 29, and month 32
Leadership in implementation teams is assessed using two scales, one for implementation team supervisors, and one for implementation team staff. Each scale has 13 items and uses a 5-point Likert ranging from "Totally disagree" to "Totally agree" to assess respondent's agreement on statements about their team supervisor (for staff) or themselves (for supervisors).
Baseline, month 25, month 29, and month 32
Cultural Exchange Inventory
Tidsramme: Baseline, month 25, month 29, and month 32
For implementation team members only: The Cultural Exchange Inventory assesses the teamwork landscape of GlobalConsent implementation teams using 7 items. Respondents give their level of agreement, using a 5-point Likert scale ranging from "Totally disagree" to "Totally agree," on statements such as "The implementation team is working well together to implement GlobalConsent" and "My colleagues are devoting a lot of time and energy to maintain the collaboration of the implementation team.
Baseline, month 25, month 29, and month 32
College Date Rape Attitudes & Behaviors Scale
Tidsramme: Baseline, month 25, month 29, and month 32
For implementation team members only: The College Date Rape Attitude Survey (CDRAS), a measure intended to assess attitudes related to the risk of committing rape in adolescents and young adults, the CDRAS measures four rape-related attitudes: Entitlement, Blame Shifting, Traditional Roles, and Overwhelming Sexual Arousal. The CDRAS contains 20 items measuring attitudes toward date rape. All items require responses on a 5-point Likert scale. The responses for the attitude scale are strongly agree, agree, neutral, disagree, and strongly disagree. Scoring is reversed for appropriate items; so that high scores (5) always correspond to the most desirable (rape-related) responses.
Baseline, month 25, month 29, and month 32
Acceptability, Feasibility, and Appropriateness of Programming to Prevent Sexually Violent Behavior among Students
Tidsramme: Baseline and up to 49 months

This scale assesses respondents' attitudes towards sexual violence prevention programming by asking them to rate their level of agreement with 10 statements, such as "Implementing sexual violence prevention programming with students at our university is something I support," "...addresses a relevant problem among our students," "…would be easy for students to participate in." These statements will be rated using a 5-point Likert scale ranging from "Totally disagree" to "Totally agree."

Surveys will be provided to all groups at different time points as follows:

  • Students: Baseline (month 10), every 6 months up to 30 months
  • Faculty: Baseline, 32 months, and 44 months
  • Leaders: Baseline and 41 months
  • Implementation Team: Baseline, month 25, month 29, and month 32
Baseline and up to 49 months
Acceptability, Feasibility, and Appropriateness of GlobalConsent
Tidsramme: Baseline and up to 49 months

This scale assesses respondents' attitudes towards the GlobalConsent program specifically by asking them to rate their level of agreement or disagreement with 10 statements, such as "Implementing GlobalConsent with students at our university is something I support," "...addresses a relevant problem among our students," "…would be easy for students to participate in." these statements will be rated using a 5-point Likert ranging from "Totally disagree" to "Totally agree."

Surveys will be provided to all groups at different time points as follows:

  • Students: Baseline (month 10), every 6 months up to 30 months.
  • Faculty: Baseline, 32 months, and 44 months
  • Leaders: Baseline and 41 months
  • Implementation Team: Baseline, month 25, month 29, and month 32
Baseline and up to 49 months
Sexual Violence Legality and Harm (Information about Sexual Activity)
Tidsramme: Baseline and up to 49 months

Knowledge of the law is assessed with 12 items where respondents indicate if they think the situations described are illegal (scored as 1), legal, but harmful (2), or legal and not harmful (3), with example items including "Forcing a person to have oral sex" and "Pressuring someone to have sex." Items will be re-coded such that responses indicating an accurate estimate or overestimate of the illegality and harms of sexual violence were coded as "1" and items indicating an underestimation of the illegality and harms of sexual violence were coded as "0".

Surveys will be provided to all groups at different time points as follows:

  • Students: Baseline (month 10), every 6 months up to 30 months.
  • Faculty: Baseline, 32 months, and 44 months
  • Leaders: Baseline and 41 months
  • Implementation Team: Baseline, month 25, month 29, and month 32
Baseline and up to 49 months
Active Consent (Information about Sexual Consent)
Tidsramme: Baseline and up to 49 months

This form adapted the Sexual Consent Scale to ask respondents to rate their level of agreement with 12 statements about sexual consent using a 5-point Likert scale ranging from "totally disagree" to "totally agree". It includes statements such as "If a person consents to sex, one can continue sexual contact even if the person changes their mind," and "Obtaining consent for sex is just as necessary in a long-term relationship as in a new relationship."

Surveys will be provided to all groups at different time points as follows:

  • Students: Baseline (month 10), every 6 months up to 30 months
  • Faculty: Baseline, 32 months, and 44 months
  • Leaders: Baseline and 41 months
  • Implementation Team: Baseline, month 25, month 29, and month 32
Baseline and up to 49 months
Rejection of Rape Myths (Attitudes about Sexual Situations)
Tidsramme: Baseline and up to 49 months

This form is a combination of the Illinois Rape Myth Acceptance Scale and the College Date Rape Attitudes & Behaviors Scale. This assesses attitudes towards sexual assault and rape by asking respondents to rate their level of agreement or disagreement with 15 statements using a 5-point Likert scale ranging from "totally disagree" to "totally agree". Statements include "If a woman dresses in a sexy dress, she is asking for sex," and "When guys rape, it is usually because of their strong desire for sex."

Surveys will be provided to all groups at different time points as follows:

  • Students: Baseline (month 10), every 6 months up to 30 months.
  • Faculty: Baseline, 32 months, and 44 months
  • Leaders: Baseline and 41 months
  • Implementation Team: Baseline, month 25, month 29, and month 32
Baseline and up to 49 months
Perceptions of Campus Attitudes
Tidsramme: Baseline and up to 49 months

This form assesses the perceptions of respondents in their university's faculty and leaders' potential response to sexual violence on their university campus. Questions ask about behaviors of abuse, sexual assault, and stalking, and their level of agreement or disagreement with whether faculty and leaders would believe a student reporting experiencing these behaviors, respect a student who reported experiencing these behaviors, or admire a student intervening in these behaviors. Agreement is assessed using a 5-point Likert scale ranging from "totally disagree" to "totally agree"

Surveys will be provided to all groups at different time points as follows:

  • Students: Baseline (month 10), every 6 months up to 30 months
  • Faculty: Baseline, 34 months, and 49 months
  • Leaders: Baseline and 41 months
  • Implementation Team: Baseline, month 25, month 29, and month 32
Baseline and up to 49 months
Empathy for Rape Victims
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
Students only: Empathy for rape victims will be assessed with a modified version of the Rape Empathy Scale (RES). This assessment includes 10 items where participants were asked to choose between two statements, one of which reflected greater empathy towards rapists ("I understand the helplessness a rapist might feel during a rape since he cannot control his actions") and one of which reflected greater empathy towards victims ("I understand the helplessness a victim might feel during a rape"). Responses are scored as 1 (more empathy for victim) or 0 (more empathy for perpetrator) and total scores range from 0 to 10 where higher scores indicate more empathy towards rape victims.
Baseline (month 10), every 6 months for up to 30 months.
Sexual Communication Attitudes
Tidsramme: Baseline (month10), every 6 months for up to 30 months.
Students only: This is a 7-item scale measuring agreement or disagreement with statements focusing on sexual communication. Agreement and disagreement is assessed using a 5-point Likert ranging from "totally disagree" to "totally agree."
Baseline (month10), every 6 months for up to 30 months.
Bystander Self-Efficacy
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
Students only: Bystander Self-Efficacy will be measured using the Bystander Efficacy Scale, which was developed for a project that evaluated the effectiveness of a sexual violence prevention program based on preventing antecedents to sexual violence by increasing prosocial bystander behavior. On this measure, participants are asked to indicate their confidence, on a 3-point scale, in performing each of 10 bystander behaviors (e.g., "Speak up to a guy who is making excuses for using physical force in a sexual relationship."). Scores are created by subtracting the mean of the 10 items from 100 to create a scale of perceived ineffectiveness; thus, higher scores indicate lesser effectiveness.
Baseline (month 10), every 6 months for up to 30 months.
Bystander Intention to Intervene (Readiness to Intervene)
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.

Students only: Readiness to Intervene will be measured using three intent-to-help subscales.

  • Intent to Help Friend Scale: Sexual Abuse
  • Intent to Help Friend Scale: Intimate Partner Violence Intent to help is an attitude that is related to bystander action. Participants will be asked how likely they are to take different bystander actions.

The second Intent to Help subscale focuses on participants' intent to help strangers in both sexual abuse and intimate partner abuse situations.

Responses range from 1 (not at all likely) to 5 (extremely likely). The average is calculated from the answers across the items to score this measure.

Baseline (month 10), every 6 months for up to 30 months.
Severity Measure for Depression
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
Students only: Depression will be measured using the Patient Health Questionnaire 9 (PHQ-9): The PHQ-9 is a multipurpose instrument for screening, diagnosing, monitoring, and measuring the severity of depression. The PHQ-9 is completed by the participant in minutes and is rapidly scored by a clinician. The PHQ-9 can also be administered repeatedly, which can reflect the improvement or the worsening of depression in response to treatment. PHQ-9 scores of 5, 10, 15, and 20 represent mild, moderate, moderately severe, and severe depression.
Baseline (month 10), every 6 months for up to 30 months.
Generalized Anxiety Disorder
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.

Students will complete the Generalized Anxiety Disorder 7-item (GAD-7), which is a quick and easy tool to help identify patients with anxiety and monitor treatment response. The GAD-7 has been validated as a diagnostic tool and a severity assessment scale. The scale consists of 7 items. The total score can range from 0 to 21, and it indicates the severity of anxiety as follows:

0 to 4: Minimal anxiety 5 to 9: Mild anxiety 10 to 14: Moderate anxiety 15 to 21: Severe anxiety

Baseline (month 10), every 6 months for up to 30 months.
Students' Proactive Bystander Behavior Scale
Tidsramme: Baseline (month 10), every 6 months up to 30 months
This scale asks respondents to indicate whether and how often they completed proactive bystander behavior actions in the last 6 months (the time between each survey wave). Behaviors include "I have encouraged others to learn more and get involved in preventing sexual or dating violence," and "I have told guys not to talk about women in sexually degrading ways," and response options for each statement are (0) No, I have not done this in the last 6 months, (1) Yes, once in the last 6 months, and (2) Yes, more than once in the last 6 months.
Baseline (month 10), every 6 months up to 30 months
Students' Reactive Bystander Action Scale
Tidsramme: Baseline (month 10), every 6 months up to 30 months
This scale asks respondents whether and how often they completed reactive bystander behavior actions in the last 6 months (the time between each survey wave). Actions include "I have expressed concern or offered help to a woman who said she had an unwanted sexual experience but didn't call it 'rape'," "I have reported formally to an authority a guy who used physical force against a women," and "I have intervened with a guy's action because I wanted to stop an act of sexual violence." Responses options for each statement are (0) I experienced this situation in the last 6 months and did NOT act, (1) Yes, once in the last 6 months, (2) Yes, more than once in the last 6 months, and (9) I did NOT experience any situation like this in the last 6 months.
Baseline (month 10), every 6 months up to 30 months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Kathryn Yount, PhD, Emory University

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

27. marts 2024

Primær færdiggørelse (Anslået)

1. februar 2028

Studieafslutning (Anslået)

1. februar 2028

Datoer for studieregistrering

Først indsendt

15. maj 2024

Først indsendt, der opfyldte QC-kriterier

29. maj 2024

Først opslået (Faktiske)

5. juni 2024

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

23. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

22. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • STUDY00006481
  • 1R01MH133259 (U.S. NIH-bevilling/kontrakt)
  • 2025P011593 (Anden identifikator: Emory Insight Humans IRB)

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

Forskerholdet vil dele tre bølger af fuldt afidentificerede paneldata med fakultetet; og 10 bølger af fuldt afidentificerede paneldata med studerende.

IPD-delingstidsramme

Data vil blive gjort tilgængelige til deling fra og med 12 måneder efter offentliggørelsen af ​​de primære målpapirer eller 12 måneder efter udløbet af præstationsperioden, alt efter hvad der kommer først.

IPD-delingsadgangskriterier

Emory Dataverse for offentligt tilgængelige data og efter rimelig anmodning til PI for eventuelle begrænsede data.

IPD-deling Understøttende informationstype

  • STUDY_PROTOCOL
  • ANALYTIC_CODE

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

produkt fremstillet i og eksporteret fra U.S.A.

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Kliniske forsøg med Vold, seksuelt

Abonner