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The Effect of a Resistance Training Program in Healthcare Workers on Pain, Workability and Physical Function.

5. oktober 2019 opdateret af: 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.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

37

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Spanien
      • Valencia, Spanien, 46010
        • Clinic Universitary Hospital of Valencia

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 og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Healthcare Workers at the Hospital
  • Informed consent

Exclusion Criteria:

  • Unable to perform exercises

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: Ikke-randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Intervention
15 minutes of resistance training at the work place every day
Andet: Resistance training
15 minutes of resistance training during work every day
Ingen indgriben: Control
Usual work

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
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
Foranstaltningsbeskrivelse
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)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

University of Valencia

Efterforskere

  • Studiestol: Jose C Granell, PhD, University of Valencia

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)

17. april 2018

Primær færdiggørelse (Faktiske)

19. juni 2018

Studieafslutning (Faktiske)

19. juni 2018

Datoer for studieregistrering

Først indsendt

13. marts 2018

Først indsendt, der opfyldte QC-kriterier

16. april 2018

Først opslået (Faktiske)

18. april 2018

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

8. oktober 2019

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

5. oktober 2019

Sidst verificeret

1. oktober 2019

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 0000260894

Plan for individuelle deltagerdata (IPD)

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