The Effect of a Resistance Training Program in Healthcare Workers on Pain, Workability and Physical Function.
5 oktober 2019 uppdaterad 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.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Faktisk)
37
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
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Valencia, Spanien, 46010
- Clinic Universitary Hospital of Valencia
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Healthcare Workers at the Hospital
- Informed consent
Exclusion Criteria:
- Unable to perform exercises
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: Intervention
15 minutes of resistance training at the work place every day
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15 minutes of resistance training during work every day
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Inget ingripande: Control
Usual work
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Pain overall status: Standard 7-point patient global impression
Tidsram: 2 days after the end of intervention (POST)
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Standard 7-point patient global impression of pain collected at the endpoint
|
2 days after the end of intervention (POST)
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Workability Index
Tidsram: Baseline
|
Questionnaire work ability
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Baseline
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Workability Index
Tidsram: 2 days after the end of intervention (POST)
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Questionnaire work ability
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2 days after the end of intervention (POST)
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Physical function
Tidsram: Baseline
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Physical tests (push-ups, Biering-Sorensen test, Sit to Stand)
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Baseline
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Physical function
Tidsram: 2 days after the end of intervention (POST)
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Physical tests (push-ups, Biering-Sorensen test, Sit to Stand)
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2 days after the end of intervention (POST)
|
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Perceived physical exertion
Tidsram: Baseline
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Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
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Baseline
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Perceived physical exertion
Tidsram: 3 weeks of resistance training
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Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
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3 weeks of resistance training
|
|
Perceived physical exertion
Tidsram: 6 weeks of resistance training
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Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
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6 weeks of resistance training
|
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Perceived physical exertion
Tidsram: 2 days after the end of intervention (POST)
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Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
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2 days after the end of intervention (POST)
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"Need for recovery scale" after work
Tidsram: Baseline
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Five point scale (1 = never, 5 = always)
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Baseline
|
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"Need for recovery scale" after work
Tidsram: 3 weeks of resistance training
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Five point scale (1 = never, 5 = always)
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3 weeks of resistance training
|
|
"Need for recovery scale" after work
Tidsram: 6 weeks of resistance training
|
Five point scale (1 = never, 5 = always)
|
6 weeks of resistance training
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"Need for recovery scale" after work
Tidsram: 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
Tidsram: Baseline
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The number of days the participants used analgesics during the last week
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Baseline
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Self-rated use of analgesics
Tidsram: 3 weeks of resistance training
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The number of days the participants used analgesics during the last week
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3 weeks of resistance training
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Self-rated use of analgesics
Tidsram: 6 weeks of resistance training
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The number of days the participants used analgesics during the last week
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6 weeks of resistance training
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Self-rated use of analgesics
Tidsram: 2 days after the end of intervention (POST)
|
The number of days the participants used analgesics during the last week
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2 days after the end of intervention (POST)
|
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Tidsram: Baseline
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Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
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Baseline
|
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Tidsram: 3 weeks of resistance training
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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)
Tidsram: 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)
Tidsram: 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)
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Studiestol: Jose C Granell, PhD, University of Valencia
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
17 april 2018
Primärt slutförande (Faktisk)
19 juni 2018
Avslutad studie (Faktisk)
19 juni 2018
Studieregistreringsdatum
Först inskickad
13 mars 2018
Först inskickad som uppfyllde QC-kriterierna
16 april 2018
Första postat (Faktisk)
18 april 2018
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
8 oktober 2019
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
5 oktober 2019
Senast verifierad
1 oktober 2019
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 0000260894
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