- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02206113
Sit to Stand Intervention for Allina Health Employees
26. januar 2015 opdateret af: Allina Health System
A Sit-to-Stand Intervention for Allina Health Employees: A Pilot Study
A 16 week pilot study for Allina call center employees to look at the psychological outcomes and biological markers after an intervention of using a standing work station.
There were two groups: group 1 received, and was instructed to use, the standing work station for all 16 weeks, group 2 was a wait-list control group and received, and was instructed to use, the standing work station for the second 8 weeks.
Psychological outcomes were measured at weeks 0, 4, 8, 12, and 16.
Biological markers were measured at weeks 0, 8, and 16.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
39
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Minnesota
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Minneapolis, Minnesota, Forenede Stater, 55407
- Allina Health
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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
18 år til 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Allina Health Call Center Employee (75% or higher employee status)
- Aged 18 to 65 years
- Provide written informed consent
Exclusion Criteria:
- Unable to stand for 20 minutes continuously unaided
- Home based employees
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Tildeling: Randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Standing workstation - 16 weeks
This arm, Standing workstation - 16 weeks, received the intervention of a standing workstation for 16 weeks.
For the first 8 weeks, the participants were instructed how long to stand per hour for an 8 hour shift.
The second 8 weeks their use was monitored for sustainability.
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Andre navne:
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Aktiv komparator: Standing workstation - second 8 weeks
This arm, Standing workstation - second 8 weeks, received the intervention of a standing workstation for 8 weeks of the study.
For the first 8 weeks, the worked at their normal desks without an intervention.
The second 8 weeks they received a standing workstation and their use was monitored.
|
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Change in self-reported quality of life
Tidsramme: Baseline, week 4, week 8, week 12, week 16
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Change in quality of life will be measured through the administration of the PROMIS-29 questionnaire.
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Baseline, week 4, week 8, week 12, week 16
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Change in waist circumference
Tidsramme: Baseline, Week 8, Week 16
|
Waist circumference measured in inches
|
Baseline, Week 8, Week 16
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Change in number of minutes stood per day
Tidsramme: Baseline, week 8, week 16
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Participants recorded their number of minutes stood at work daily from baseline through week 16.
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Baseline, week 8, week 16
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Change in self-reported stress
Tidsramme: Baseline, week 4, week 8, week 12, week 16
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Change in stress will be measured through the administration of the Perceived Stress Scale (PSS).
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Baseline, week 4, week 8, week 12, week 16
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Change in health promotion and lifestyle choices
Tidsramme: Baseline, week 4, week 8, week 12, week 16
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Change in health promotion and lifestyle choices will be measured through the administration of the Health Promoting Lifestyle Profile Questionnaire (HPLP-II).
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Baseline, week 4, week 8, week 12, week 16
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Change in workplace productivity
Tidsramme: Baseline, week 4, week 8, week 12, week 16
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Change in workplace productivity will be measured through the administration of Workplace Productivity and Activity Impairment (WPAI) questionnaire.
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Baseline, week 4, week 8, week 12, week 16
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Change in self-reported physical activity levels
Tidsramme: Baseline, week 4, week 8, week 12, week 16
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Change in self-reported physical activity levels will be measured through the administration of the International Physical Activity Questionnaire (IPAQ)
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Baseline, week 4, week 8, week 12, week 16
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Change in Body Mass Index (BMI)
Tidsramme: Baseline, Week 8, Week 16
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Change in an individual's BMI after being weighed at baseline, week 8, and week 16.
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Baseline, Week 8, Week 16
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Change in body fat percentage
Tidsramme: Baseline, week 8, week 16
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Change in body fat percentage as measured by a BodPod® Assessment.
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Baseline, week 8, week 16
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Change in resting heart rate
Tidsramme: Baseline, week 8, week 16
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Change in resting heart rate from baseline to week 16.
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Baseline, week 8, week 16
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Change in blood pressure (systolic and diastolic)
Tidsramme: Baseline, week 8, week 16
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Change in both systolic and diastolic blood pressure from baseline to week 16.
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Baseline, week 8, week 16
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Jeffery Dusek, PhD, Allina Health
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. maj 2013
Primær færdiggørelse (Faktiske)
1. november 2013
Studieafslutning (Faktiske)
1. november 2013
Datoer for studieregistrering
Først indsendt
28. juli 2014
Først indsendt, der opfyldte QC-kriterier
31. juli 2014
Først opslået (Skøn)
1. august 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
28. januar 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
26. januar 2015
Sidst verificeret
1. januar 2015
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- 3989-1
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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