- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02807831
A Randomized Clinical Trial Comparing Executive Function and Language Skills Training on School Readiness in Preschool Children
16. juni 2016 opdateret af: Guilherme Vanoni Polanczyk, University of Sao Paulo
Background: environmental influences in the first years of life have a great impact on adulthood.
Adequate environmental stimulation in the first years of life positively influence cognitive, emotional and neurological development.
Studies show that high quality education for 3 to 6 years old children are cost-effective for diverse outcomes, such as socioemotional and cognitive development, as well as school performance.
However, it is not clear why specific types of interventions are most effective on school readiness, an important precursor of literacy status and later life outcomes.
Objectives: adapt to the Brazilian context two well-known intervention programs: (1) executive functions training developed by Diamond, and (2) oral language skills based on the Nuffield Programme developed by Snowling and colleagues.
Methods: a randomized controlled trial involving 720 children (4 to 5 years old) allocated to three groups: (1) adapted school curriculum focusing on executive functions training, (2) adapted school curriculum focusing on oral language skills training, and (3) regular school curriculum.
Studieoversigt
Status
Afsluttet
Betingelser
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
582
Fase
- Ikke anvendelig
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
3 år til 6 år (Barn)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Schools interested in the intervention program
- Preschool children (4 to 6 years old)
Exclusion Criteria:
- Presence of any sensory impairment
- Intellectual disability
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: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Executive functions training
|
Daily training of executive functions via activities to develop auto-regulation, attention and memory.
|
|
Eksperimentel: Language skills training
|
Daily training of language skills via activities to develop phonological awareness and vocabulary.
|
|
Aktiv komparator: Regular school curriculum
|
Ministry of Education national school curriculum.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in school readiness
Tidsramme: Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
Assessed with a 43 items questionnaire developed by the research staff.
|
Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in inhibitory control
Tidsramme: Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
Inhibitory control assessed via the Flanker e Simon (Dots task) tests.
|
Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
|
Change in working memory
Tidsramme: Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
Working memory assessed via the neuropsychological Automated Working Memory Assessment (AWMA).
|
Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
|
Change in oral language skills
Tidsramme: Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
Expressive language assessed via the Child Language Test - ABFW.
|
Beginning of the school year (baseline) and at the end of the school year (post intervention, 7 to 8 months later)
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
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
1. februar 2014
Primær færdiggørelse (Faktiske)
1. december 2014
Studieafslutning (Faktiske)
1. december 2014
Datoer for studieregistrering
Først indsendt
10. juni 2016
Først indsendt, der opfyldte QC-kriterier
16. juni 2016
Først opslået (Skøn)
21. juni 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
21. juni 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
16. juni 2016
Sidst verificeret
1. juni 2016
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 2012/51.624-1
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 .
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-
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-
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