- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02672215
RCT Computer-tailored Intervention on Workplace Sitting (StartToStand)
3. december 2021 opdateret af: University Ghent
The Effectiveness of a Web-based Computer-tailored Intervention on Workplace Sitting: a Randomized Controlled Trial
A theory-driven, web-based, computer-tailored advice to influence sitting at work was developed.
The study investigated the effects of this computer-tailored intervention to influence workplace sitting on behavioural measures.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The study investigated the effects of the theory-driven, web-based, computer-tailored intervention to influence workplace sitting on objectively measured sitting time, standing time and breaks from sitting, as well as self-reported context-specific sitting.
The computer-tailored advice was compared to a generic advice and a 'no-advice' control at 1-month and 3-months follow-up.
The 'tailored' group received a web-based computer-tailored intervention including personalized feedback and tips on how to reduce and/or interrupt workplace sitting.
The 'generic' group received a web-based intervention containing generic information and tips to reduce and/or interrupt workplace sitting.
The control group was a waitlist control condition and received the generic intervention after completing all measurements.
Participants were recruited from a convenience sample of two companies (university and environmental agency) in Flanders (i.e.
northern Dutch-speaking part of Belgium), mainly employing desk-based workers, having more than 100 staff members and each having at least three different worksite locations.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
1061
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
18 år til 70 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- being employed
Exclusion Criteria:
- not being able to stand
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Faktoriel opgave
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: tailored group
Received a web-based computer-tailored intervention including personalized feedback and tips on how to reduce and/or interrupt workplace sitting.
|
web-based computer-tailored intervention including personalized feedback and tips on how to reduce and/or interrupt workplace sitting
|
|
Aktiv komparator: generic group
Received a web-based intervention containing generic information and tips to reduce and/or interrupt workplace sitting.
|
general, non-tailored web-based generic advice with tips
|
|
Ingen indgriben: control group
A waitlist control condition and received the generic intervention after completing all measurements
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
sitting time
Tidsramme: one week
|
objectively measured sitting time with ActivPAL
|
one week
|
|
self-reported context-specific sitting time
Tidsramme: one week
|
self-reported context-specific sitting time with WSQ questionnaire
|
one week
|
|
standing time
Tidsramme: one week
|
objectively measured standing time with ActivPAL
|
one week
|
|
breaks from sitting
Tidsramme: one week
|
objectively measured breaks from sitting with ActivPAL
|
one week
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
psychosocial correlates of sitting
Tidsramme: one week
|
psychosocial correlates of sitting with questionnaire
|
one week
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- De Cocker K, De Bourdeaudhuij I, Cardon G, Vandelanotte C. What are the working mechanisms of a web-based workplace sitting intervention targeting psychosocial factors and action planning? BMC Public Health. 2017 May 3;17(1):382. doi: 10.1186/s12889-017-4325-5.
- De Cocker K, De Bourdeaudhuij I, Cardon G, Vandelanotte C. The Effectiveness of a Web-Based Computer-Tailored Intervention on Workplace Sitting: A Randomized Controlled Trial. J Med Internet Res. 2016 May 31;18(5):e96. doi: 10.2196/jmir.5266.
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)
30. september 2014
Primær færdiggørelse (Faktiske)
31. marts 2015
Studieafslutning (Faktiske)
31. oktober 2017
Datoer for studieregistrering
Først indsendt
20. januar 2016
Først indsendt, der opfyldte QC-kriterier
31. januar 2016
Først opslået (Skøn)
3. februar 2016
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
6. december 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
3. december 2021
Sidst verificeret
1. december 2021
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- EC/2012/320
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 .