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Testing the Effectiveness of Relationship Smarts and the Effects of Enhanced Facilitator Training

13. mai 2019 oppdatert av: Mathematica Policy Research, Inc.

Testing the Effectiveness of Relationship Smarts Curriculum and the Effects of Enhanced Facilitator Training

This project will test the effectiveness of offering healthy marriage and relation education for youth as part of the regular school curriculum and examine whether providing enhanced training and support for facilitators shows promise for enhancing the effects on high school students. The evaluation will examine a range of students' relationship outcomes, including their attitudes toward relationships, their knowledge of healthy relationships, their communication skills, and the characteristics of their current relationship.

Studieoversikt

Status

Tilbaketrukket

Forhold

Detaljert beskrivelse

Family Bridges will deliver the "Relationship Smarts +" program to students at 10 Chicago-area high schools. The RS+ curriculum will be delivered to 9th grade students in the target schools and classrooms during the 2016-2017 and 2017-2018 school years. The curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week.The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making. Using a three-arm randomized controlled trial design, this study will test the effectiveness of offering RS+ as part of the regular school curriculum on the students' knowledge of healthy relationships, their communication skills, and the characteristics of their current relationship. In addition to testing the effects of the curriculum, the study will also test the effects of providing enhanced training and support to facilitators.

Studietype

Intervensjonell

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

    • Illinois
      • Oak Park, Illinois, Forente stater, 60302
        • Family Bridges, Inc.

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

Ikke eldre enn 17 år (Barn)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Students must be age 17 or younger
  • have consent from a parent or guardian for evaluation activities
  • provide assent for evaluation activities.

Exclusion Criteria:

  • Students in evaluation classrooms who do not meet these criteria will still receive programming, but will not be included in the STREAMS data collection activities or in the study's analysis.

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: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: Control
Control group members will receive an alternate curriculum that is not related to relationship education. Family Bridges has identified a computer programming curriculum, Codeacademy, that teaches students how to use HTML.
a computer programming curriculum, Codeacademy, that teaches students how to use HTML.
Eksperimentell: RS+
The RS+ curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week. The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.
The curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week. The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.
Eksperimentell: RS+ with enhanced facilitator support
The RS+ curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week. The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making. Affiliates assigned to this enhanced treatment group will participate in enhanced facilitator training and support activities.
The curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week. The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Knowledge about Healthy Relationships
Tidsramme: end of programming (approx. 12 weeks after beginning of programming )
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
end of programming (approx. 12 weeks after beginning of programming )
Attitudes about Healthy Relationships
Tidsramme: end of programming (approx. 12 weeks after beginning of programming )
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
end of programming (approx. 12 weeks after beginning of programming )
Knowledge about Healthy Relationships
Tidsramme: 1 year follow-up
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
1 year follow-up
Attitudes about Healthy Relationships
Tidsramme: 1 year follow-up
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
1 year follow-up

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Communications skills
Tidsramme: end of programming (approx. 12 weeks after beginning of programming )
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
end of programming (approx. 12 weeks after beginning of programming )
Characteristics of current romantic relationship
Tidsramme: end of programming (approx. 12 weeks after beginning of programming )
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
end of programming (approx. 12 weeks after beginning of programming )
Communications skills
Tidsramme: 1 year follow-up
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
1 year follow-up
Characteristics of current romantic relationship
Tidsramme: 1 year follow-up
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
1 year follow-up

Samarbeidspartnere og etterforskere

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

Etterforskere

  • Hovedetterforsker: Diane Paulsell, Mathematica Policy Research

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)

1. desember 2016

Primær fullføring (Faktiske)

1. januar 2018

Studiet fullført (Faktiske)

1. januar 2018

Datoer for studieregistrering

Først innsendt

2. juni 2016

Først innsendt som oppfylte QC-kriteriene

8. juli 2016

Først lagt ut (Anslag)

13. juli 2016

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

15. mai 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

13. mai 2019

Sist bekreftet

1. mai 2019

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • MPR-500098-FB

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

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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