- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02831413
Testing the Effectiveness of Relationship Smarts and the Effects of Enhanced Facilitator Training
13. maj 2019 opdateret af: 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.
Studieoversigt
Status
Trukket tilbage
Intervention / Behandling
Detaljeret 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.
Undersøgelsestype
Interventionel
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
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Illinois
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Oak Park, Illinois, Forenede Stater, 60302
- Family Bridges, Inc.
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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
Ikke ældre end 17 år (Barn)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
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
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / 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.
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a computer programming curriculum, Codeacademy, that teaches students how to use HTML.
|
|
Eksperimentel: 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.
|
|
Eksperimentel: 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.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
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.
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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 |
Foranstaltningsbeskrivelse |
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
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Diane Paulsell, Mathematica Policy Research
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)
1. december 2016
Primær færdiggørelse (Faktiske)
1. januar 2018
Studieafslutning (Faktiske)
1. januar 2018
Datoer for studieregistrering
Først indsendt
2. juni 2016
Først indsendt, der opfyldte QC-kriterier
8. juli 2016
Først opslået (Skøn)
13. juli 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
15. maj 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
13. maj 2019
Sidst verificeret
1. maj 2019
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- MPR-500098-FB
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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 .