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Impact Evaluation of Training Civil Servants on Violence Against Women in Medellín, Colombia

6. februar 2017 oppdatert av: Econometría Consultores

Capacity of State and Local Actors to Respond to Violence Against Women: Impact Evaluation of Training Civil Servants on Violence Against Women in Medellín (Colombia), Component of the Program "Seguridad Pública"

The purpose of this study is to determine whether the training of civil servants leads to a reduction in the violence suffered by women, as well as in their psychological wellbeing and attitudes towards violence.

Studieoversikt

Detaljert beskrivelse

The Secretary of Women of Medellin, through the ICONTEC, intends to conduct training to officials of the 22 family commissioners in Medellin. The objective of these trainings is to standardize procedures in order that women do not feel re-victimized and can forward complaints. Since the training will be done in phases in 2014 and there is willingness of relevant stakeholders to generate a random order on which commissioners the training is first performed, it can be done a cluster randomized trial.

We will require all 22 commissioners to be randomly assigned into two groups, one treatment and one control. To implement it is intended to:

  • Conduct a baseline survey amongst women who used the services of the commissionaires between June and Septmber 2013, completed the process of care and signed informed consent.
  • Training of a randomly chosen set of 11 commissioners will take place between June and September 2014.
  • Conduct an endline survey amongst women who used the services of any of the 22 commissionaires between June and September 2014, completed the process of care and signed informed consent.

Women will be contacted through the commissioners. Women who have completed the process of care will be ask whether they want to participate in the study. If they agree, their contact details will transfer to the investigators for the survey to be conducted. This process would be conducted twice for baseline information before beginning the training, and for endline, once half of the first 11 commissioners have been trained.

Studietype

Intervensjonell

Registrering (Faktiske)

975

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

      • Bogota, Colombia
        • Econometria Consultores

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

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

Inclusion Criteria:

  • Women who initiate and finalize the process with the comissaries of family

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Trained
Training civil servants in Medellin (Colombia) on attention to violence against women.
The Secretary of Women of Medellin, through the ICONTEC, intends to conduct training to officials of the 22 family commissioners in Medellin. The objective of these trainings is to standardize procedures in order that women do not feel re-victimized and can forward complaints.
Ingen inngripen: Non trained

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Occurrence of violence
Tidsramme: 3 months
The outcome will be measure through a survey to women who used the services of the commissionaires, completed the process of care and signed informed consent
3 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Knowledge, attitudes and practices (KAP) on violence and care pathways
Tidsramme: Average of 8 months after the complaint was presented at the comissaries
The outcome will be measure through a survey to women who used the services of the commissionaires, completed the process of care and signed informed consent
Average of 8 months after the complaint was presented at the comissaries
Psychological well-being (self-acceptance, positive relationships, autonomy, environmental mastery, personal growth, purpose in life)
Tidsramme: Average of 8 months after the complaint was presented at the comissaries
The outcome will be measure through a survey to women who used the services of the commissionaires, completed the process of care and signed informed consent
Average of 8 months after the complaint was presented at the comissaries
Time resolution of cases
Tidsramme: Average of 8 months after the complaint was presented at the comissaries
The outcome will be measured through secondary data of the commissaries with information between the time of the initiation of the complaint and the completed the process of care.
Average of 8 months after the complaint was presented at the comissaries

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

1. mai 2014

Primær fullføring (Faktiske)

1. november 2015

Studiet fullført (Faktiske)

1. juni 2016

Datoer for studieregistrering

Først innsendt

28. mai 2014

Først innsendt som oppfylte QC-kriteriene

2. juni 2014

Først lagt ut (Anslag)

3. juni 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

7. februar 2017

Siste oppdatering sendt inn som oppfylte QC-kriteriene

6. februar 2017

Sist bekreftet

1. februar 2017

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • ATN/MG-13064-RG ECO 577-3

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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