- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT06443541
Strategier for implementering af globalt samtykke for at forhindre seksuel vold hos universitetsmænd (SCALE)
SKALA: Strategier til implementering af globalt samtykke til forebyggelse af seksuel vold hos universitetsmænd
Studieoversigt
Status
Betingelser
Intervention / Behandling
- Adfærdsmæssigt: Lav-intensitet implementeringsstrategier (LIS) for studerende
- Andet: Højintensive implementeringsstrategier (HIS) for fakultetet
- Andet: Lav-intensitet implementeringsstrategier (LIS) for fakultetet
- Andet: Højintensive implementeringsstrategier (HIS) for ledere
- Andet: Lav-intensitet implementeringsstrategier (LIS) for ledere
- Andet: Højintensive implementeringsstrategier (HIS) for implementeringsteammedlemmer
- Andet: Lav-intensitet implementeringsstrategier (LIS) Implementeringsteammedlemmer
- Adfærdsmæssigt: High-intensity implementation strategies (HIS)-Students
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
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: Kathryn Yount, PhD
- Telefonnummer: 404-727-8511
- E-mail: kathryn.yount@emory.edu
Studiesteder
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Can Tho, Vietnam
- Rekruttering
- Can Tho University of Medicine and Pharmacy (CTUMP)
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Da Nang, Vietnam
- Rekruttering
- Da Nang University of Medical Technology & Pharmacy (DUMTP)
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Haiphong, Vietnam
- Rekruttering
- Hai Phong University of Medicine and Pharmacy
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Hanoi, Vietnam, 116001
- Rekruttering
- Hanoi Medical University
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Kontakt:
- Tran Hung Minh, MD, MSc
- Telefonnummer: 0243 5770261
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Ho Chi Minh City, Vietnam
- Rekruttering
- Ho Chi Minh City Medicine and Pharmacy University
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Ho Chi Minh City, Vietnam
- Rekruttering
- Hong Bang University
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Huế, Vietnam, 470000
- Rekruttering
- Hue University of Medicine and Pharmacy
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
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
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Eksperimentel: Studerende
Studerende i begge randomiseringsgrupper bliver aktive forbrugere af GlobalConsent med en e-mailintroduktion til programmet, proces, leveringsplan, dataindsamlingsprocedurer og samtykke.
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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:
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:
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Eksperimentel: Fakultet
Fakultetet vil modtage adgang til undervisningsmateriale baseret på universitetets randomiseringsimplementeringsstrategigruppe.
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Andre navne:
Passiv adgang til webbaseret undervisningsmateriale
Andre navne:
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Eksperimentel: Ledere
Ledere vil modtage stedspecifikke (universitet) invitationer og materiale baseret på implementeringsstrategigruppen.
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Andre navne:
Andre navne:
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Eksperimentel: Medlemmer af implementeringsteam
Medlemmer af implementeringsteamet vil modtage passiv adgang til webbaseret materiale og træning i henhold til den universitetsspecifikke implementeringsstrategigruppe.
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Andre navne:
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
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Students' Reported Prosocial Bystander Behavior
Tidsramme: Baseline (month 10), every 6 months up to 30 months
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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.
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Baseline (month 10), every 6 months up to 30 months
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Students' reported Sexually Violent Behavior
Tidsramme: Baseline (month 10), every 6 months up to 30 months
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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.
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Baseline (month 10), every 6 months up to 30 months
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Handicapvurdering og tidsplan
Tidsramme: Baseline
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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
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Diagnostisk og statistisk manual (DSM)-5 Måling af krydsskæringssymptom
Tidsramme: Baseline
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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
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Baseline
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Alkoholnedsættelse Viden/virkninger af alkohol på kognition
Tidsramme: Baseline, hver 6. måned i op til 30 måneder.
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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".
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Baseline, hver 6. måned i op til 30 måneder.
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Perceptions of Sexual Violence form at their respective university
Tidsramme: Baseline (month 10) and up to 49 months
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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:
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Baseline (month 10) and up to 49 months
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Implementation Team Scale for staff and supervisors
Tidsramme: Baseline, month 25, month 29, and month 32
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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).
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Baseline, month 25, month 29, and month 32
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Cultural Exchange Inventory
Tidsramme: Baseline, month 25, month 29, and month 32
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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.
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Baseline, month 25, month 29, and month 32
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College Date Rape Attitudes & Behaviors Scale
Tidsramme: Baseline, month 25, month 29, and month 32
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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.
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Baseline, month 25, month 29, and month 32
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Acceptability, Feasibility, and Appropriateness of Programming to Prevent Sexually Violent Behavior among Students
Tidsramme: Baseline and up to 49 months
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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:
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Baseline and up to 49 months
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Acceptability, Feasibility, and Appropriateness of GlobalConsent
Tidsramme: Baseline and up to 49 months
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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:
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Baseline and up to 49 months
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Sexual Violence Legality and Harm (Information about Sexual Activity)
Tidsramme: Baseline and up to 49 months
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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:
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Baseline and up to 49 months
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Active Consent (Information about Sexual Consent)
Tidsramme: Baseline and up to 49 months
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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:
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Baseline and up to 49 months
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Rejection of Rape Myths (Attitudes about Sexual Situations)
Tidsramme: Baseline and up to 49 months
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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:
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Baseline and up to 49 months
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Perceptions of Campus Attitudes
Tidsramme: Baseline and up to 49 months
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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:
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Baseline and up to 49 months
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Empathy for Rape Victims
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
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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.
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Baseline (month 10), every 6 months for up to 30 months.
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Sexual Communication Attitudes
Tidsramme: Baseline (month10), every 6 months for up to 30 months.
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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."
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Baseline (month10), every 6 months for up to 30 months.
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Bystander Self-Efficacy
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
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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.
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Baseline (month 10), every 6 months for up to 30 months.
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Bystander Intention to Intervene (Readiness to Intervene)
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
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Students only: Readiness to Intervene will be measured using three intent-to-help subscales.
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.
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Severity Measure for Depression
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
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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.
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Baseline (month 10), every 6 months for up to 30 months.
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Generalized Anxiety Disorder
Tidsramme: Baseline (month 10), every 6 months for up to 30 months.
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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.
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Students' Proactive Bystander Behavior Scale
Tidsramme: Baseline (month 10), every 6 months up to 30 months
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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.
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Baseline (month 10), every 6 months up to 30 months
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Students' Reactive Bystander Action Scale
Tidsramme: Baseline (month 10), every 6 months up to 30 months
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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.
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Baseline (month 10), every 6 months up to 30 months
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Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Kathryn Yount, PhD, Emory University
Publikationer og nyttige links
Generelle publikationer
- Yount KM, Whitaker D, Fang X, Trang QT, Macaulay M, Hung MT. Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men (SCALE): Study Protocol for a National Implementation Trial. Res Sq [Preprint]. 2024 Sep 10:rs.3.rs-4745916. doi: 10.21203/rs.3.rs-4745916/v1.
- Yount KM, Whitaker DJ, Fang X, Trang QT, Macaulay M, Minh TH. Strategies for Implementing GlobalConsent to Prevent Sexual Violence in University Men (SCALE): study protocol for a national implementation trial. Trials. 2024 Aug 29;25(1):571. doi: 10.1186/s13063-024-08401-5.
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
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)?
IPD-planbeskrivelse
IPD-delingstidsramme
IPD-delingsadgangskriterier
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- ANALYTIC_CODE
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
produkt fremstillet i og eksporteret fra U.S.A.
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
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Ivix LLXAfsluttetHypoactive Sexual Desire Disorder (HSDD)Den Russiske Føderation
-
Ivix LLXAfsluttetHypoactive Sexual Desire Disorder (HSDD)Den Russiske Føderation
-
University of British ColumbiaAfsluttetHypoactive Sexual Desire Disorder (HSDD)Canada
-
Warner ChilcottAfsluttetHypoactive Sexual Desire Disorder (HSDD)Forenede Stater, Australien, Canada
-
EndoCeutics Inc.AMAG Pharmaceuticals, Inc.Trukket tilbageHypoactive Sexual Desire Disorder (HSDD)Forenede Stater
-
TriHealth Inc.TriHealth Medical Education Research FundAfsluttetHypoactive Sexual Desire Disorder (HSDD) | Lav libido | Kvindelig seksuel dysfunktion (FSD)Forenede Stater