The Effect of a Resistance Training Program in Healthcare Workers on Pain, Workability and Physical Function.
5. oktober 2019 oppdatert av: José Casaña Granell, University of Valencia
The Effect of a Brief Daily Resistance Training Program in Healthcare Workers on Pain, Workability and Physical Function.
The prevalence and consequences of musculoskeletal pain is considerable among healthcare workers, allegedly due to high physical work demands of healthcare work.
Performing physical exercise at the workplace together with colleagues may be more motivating for some employees and thus increase adherence. On the other hand, physical exercise performed during working hours at the workplace may be costly for the employers in terms of time spend. Thus, it seems relevant to perform a brief intervention. This study is intended to investigate the difference between the effect of workplace-based physical exercise (using elastic bands and body weight exercises) and a group control on musculoskeletal pain, physical exertion during work, physical function, need for recovery, self-rated use of analgesics, and work ability among healthcare workers.
Studieoversikt
Status
Fullført
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
37
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
-
Valencia, Spania, 46010
- Clinic Universitary Hospital of Valencia
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Healthcare Workers at the Hospital
- Informed consent
Exclusion Criteria:
- Unable to perform exercises
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Intervention
15 minutes of resistance training at the work place every day
|
15 minutes of resistance training during work every day
|
|
Ingen inngripen: Control
Usual work
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Pain overall status: Standard 7-point patient global impression
Tidsramme: 2 days after the end of intervention (POST)
|
Standard 7-point patient global impression of pain collected at the endpoint
|
2 days after the end of intervention (POST)
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Workability Index
Tidsramme: Baseline
|
Questionnaire work ability
|
Baseline
|
|
Workability Index
Tidsramme: 2 days after the end of intervention (POST)
|
Questionnaire work ability
|
2 days after the end of intervention (POST)
|
|
Physical function
Tidsramme: Baseline
|
Physical tests (push-ups, Biering-Sorensen test, Sit to Stand)
|
Baseline
|
|
Physical function
Tidsramme: 2 days after the end of intervention (POST)
|
Physical tests (push-ups, Biering-Sorensen test, Sit to Stand)
|
2 days after the end of intervention (POST)
|
|
Perceived physical exertion
Tidsramme: Baseline
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
Baseline
|
|
Perceived physical exertion
Tidsramme: 3 weeks of resistance training
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
3 weeks of resistance training
|
|
Perceived physical exertion
Tidsramme: 6 weeks of resistance training
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
6 weeks of resistance training
|
|
Perceived physical exertion
Tidsramme: 2 days after the end of intervention (POST)
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
2 days after the end of intervention (POST)
|
|
"Need for recovery scale" after work
Tidsramme: Baseline
|
Five point scale (1 = never, 5 = always)
|
Baseline
|
|
"Need for recovery scale" after work
Tidsramme: 3 weeks of resistance training
|
Five point scale (1 = never, 5 = always)
|
3 weeks of resistance training
|
|
"Need for recovery scale" after work
Tidsramme: 6 weeks of resistance training
|
Five point scale (1 = never, 5 = always)
|
6 weeks of resistance training
|
|
"Need for recovery scale" after work
Tidsramme: 2 days after the end of intervention (POST)
|
Five point scale (1 = never, 5 = always)
|
2 days after the end of intervention (POST)
|
|
Self-rated use of analgesics
Tidsramme: Baseline
|
The number of days the participants used analgesics during the last week
|
Baseline
|
|
Self-rated use of analgesics
Tidsramme: 3 weeks of resistance training
|
The number of days the participants used analgesics during the last week
|
3 weeks of resistance training
|
|
Self-rated use of analgesics
Tidsramme: 6 weeks of resistance training
|
The number of days the participants used analgesics during the last week
|
6 weeks of resistance training
|
|
Self-rated use of analgesics
Tidsramme: 2 days after the end of intervention (POST)
|
The number of days the participants used analgesics during the last week
|
2 days after the end of intervention (POST)
|
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Tidsramme: Baseline
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
Baseline
|
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Tidsramme: 3 weeks of resistance training
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
3 weeks of resistance training
|
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Tidsramme: 6 weeks of resistance training
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
6 weeks of resistance training
|
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Tidsramme: 2 days after the end of intervention (POST)
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
2 days after the end of intervention (POST)
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Studiestol: Jose C Granell, PhD, University of Valencia
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
17. april 2018
Primær fullføring (Faktiske)
19. juni 2018
Studiet fullført (Faktiske)
19. juni 2018
Datoer for studieregistrering
Først innsendt
13. mars 2018
Først innsendt som oppfylte QC-kriteriene
16. april 2018
Først lagt ut (Faktiske)
18. april 2018
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
8. oktober 2019
Siste oppdatering sendt inn som oppfylte QC-kriteriene
5. oktober 2019
Sist bekreftet
1. oktober 2019
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 0000260894
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .