- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01878097
Evaluation of Green Dot a Primary Prevention Intervention
Green Dot Across the Bluegrass: Evaluation of a Primary Prevention Intervention
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
-
-
Kentucky
-
Lexington, Kentucky, Stati Uniti, 40536-0293
- University of Kentucky
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
Only high school students attending the intervention or comparison high schools will be eligible. Two groups will be recruited: those receiving bystanding training and those not receiving such training who may or may not be in the social network of those receiving bystanding training.
Exclusion Criteria:
All other high school students in Kentucky
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
---|---|
Sperimentale: Green Dot Bystander Training
Green Dot intervention
|
Intervention allocated at the school level
|
Comparatore attivo: Control
Awareness Eduation
|
Awareness Education
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Average Number of Sexual Assault Events Used (Perpetrated) Per School.
Lasso di tempo: up to 5 years follow up from baseline intervention
|
Students self report of sexual assault perpetration averaged at the school level and adjusted for baseline and number of students.
Adjustments were made by including baseline measure and number of students as a covariate in the model.
Data will be collected at baseline and annually for 4 years.
|
up to 5 years follow up from baseline intervention
|
Average Number of Sexual Assaults Experienced (Victimization) Events Per School.
Lasso di tempo: Data will be collected at baseline and annually for 4 years.
|
Students self report of sexual assault victimization averaged at the school level and adjusted for baseline and number of students.
Adjustments made by including baseline measure and number of students as covariates in models.
Data will be collected at baseline and annually for 4 years.
|
Data will be collected at baseline and annually for 4 years.
|
Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
---|---|---|
Change in Violence Acceptance
Lasso di tempo: Data will be collected at baseline and annually for 4 years.
|
Illinois Rape Myth Acceptance Scale measure students' beliefs about rape which may indicate social norms supporting sexual violence. The scale consists of 22 questions scored 1 -5. Were 1 is "strongly agree" and 5 is "strongly disagree". The higher the cumulative score, the more likely the participant is to accept rape myths. 5-item Acceptance of General Dating Violence Scale was used to measure norms supporting dating violence. Scores will range from 1-6, were the higher the score the more likely the participant was to reject dating violence as normal. |
Data will be collected at baseline and annually for 4 years.
|
Increase in Bystanding Behaviors
Lasso di tempo: Data will be collected at baseline and annually for 4 years.
|
7 item survey measuring self-reports of students actively engaging their peers in behaviors that may prevent violence. Response options: 0 times, 1-2 times, 3-5 times, 6-9 times, 10 or more times, didn't see or hear someone doing this Above items repeated to measure student observing others doing these behaviors. Data will be presented as the total number of interventions were the bigger the number the more likely the bystander was to intervene on behalf of the victim. |
Data will be collected at baseline and annually for 4 years.
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Ann L. Coker, PhD, University of Kentucky
Pubblicazioni e link utili
Pubblicazioni generali
- Coker AL, Bush HM, Cook-Craig PG, DeGue SA, Clear ER, Brancato CJ, Fisher BS, Recktenwald EA. RCT Testing Bystander Effectiveness to Reduce Violence. Am J Prev Med. 2017 May;52(5):566-578. doi: 10.1016/j.amepre.2017.01.020. Epub 2017 Mar 6.
- Coker AL, Bush HM, Brancato CJ, Clear ER, Recktenwald EA. Bystander Program Effectiveness to Reduce Violence Acceptance: RCT in High Schools. J Fam Violence. 2019;34(3):153-164. doi: 10.1007/s10896-018-9961-8. Epub 2018 Apr 2.
- Mennicke AM, Bush HM, Brancato CJ, Coker AL. Bystander Program to Reduce Sexual Violence by Witnessing Parental Intimate Partner Violence Status. Am J Prev Med. 2022 Aug;63(2):262-272. doi: 10.1016/j.amepre.2021.12.022. Epub 2022 Mar 9.
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- 5U01CE001675 (Sovvenzione/contratto NIH degli Stati Uniti)
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .