- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT02071420
Efficacy of a Combined Ergonomic Health Promotion Intervention on Employee Health
Studieöversikt
Status
Betingelser
Detaljerad beskrivning
Primary Aim: To compare the effects of providing sedentary employees with seated active workstations in combination with an ergonomic intervention and regular motivational emails (experimental group) against the ergonomic intervention and regular emails only (active control group) on occupational sedentary behavior over 16 weeks.
Hypothesis: The addition of a seated active workstation will result in significant reductions in daily occupational sedentary time compared to the active control group.
Secondary Aims: To compare the effects of the experimental group against the active control group on secondary measures of cardiometabolic disease risk factors, musculoskeletal discomfort, cognitive function and work productivity.
Hypothesis 1: The experimental group will result in reduced cardiometabolic disease risk, musculoskeletal discomfort and work limitations compared to the active control group.
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
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Iowa
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Iowa City, Iowa, Förenta staterna, 52242
- University of Iowa
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- We will recruit overweight/obese (body mass index 25.0-40.0 kg/m2) adults (18-65 years) working in full-time (minimum 35 hours/week), sedentary (self-report sitting >75% work time) occupations at an independent work site.
Exclusion Criteria:
- Working in an office that will not meet the space or electrical requirements of the active workstation, acute or chronic illness not under treatment of a provider, orthopedic limitations that prohibit physical activity, current or planned pregnancy, hospitalization from a physical or mental disorder in the past six months and/or taking medication that may impair physical activity
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Experimentell: Experimental Group
This group will receive the seated active workstation intervention, the ergonomic intervention and the email intervention for 16 weeks.
|
Participants in the experimental group will receive a seated active workstation at their work setting for 16 weeks.
Participants of both arms will receive a face to face ergonomic workstation optimization intervention.
This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Participants of both arms will receive three emails per week for 16 weeks.
Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
|
Aktiv komparator: Active Control
This group will receive the ergonomic intervention and email intervention only for 16 weeks.
This group will not receive a seated active workstation.
|
Participants of both arms will receive a face to face ergonomic workstation optimization intervention.
This consultation will take 30 minutes to complete and will be performed at the participant's actual work station.
Participants of both arms will receive three emails per week for 16 weeks.
Messages will be consistent with what they hear in the ergonomic intervention (e.g., encourage taking breaks from sitting at work and adjusting posture to be in line with ergonomic principles).
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change in Occupational Physical Activity From Baseline to 16 Weeks
Tidsram: Baseline and 16 weeks
|
Occupational physical activity (primary outcome) will be measured objectively with the GENEActiv physical activity monitor.
The monitor will be worn on the right ankle and will be worn for 5 working days during all non-bathing hours.
The outcome measure will be change in occupational activity (average counts/work day) from baseline to 16 weeks.
The measure will be calculated as follows: 16 weeks value - baseline value.
|
Baseline and 16 weeks
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Samarbetspartners och utredare
Sponsor
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 201306711
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