- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02172053
Resistance Exercise to Improve Fatigue in Workplace (REW) (REW)
16. april 2019 opdateret af: Rosimeire Simprini Padula
Effectiveness of a Resistance Training Program in the Workplace to Muscle Fatigue Control in Industrial Workers: Cluster Randomized Controlled Trial.
Studies show that exercise resistance in workplace can reduce the symptoms of induced labor, however, the effectiveness of such programs depends on the characteristics of the training fatigue.
Thus, it is expected that this study the intervention group with training heavy using progressive resistance exercise protocol will be better in reducing fatigue when compare with light training group.
Studieoversigt
Status
Afsluttet
Betingelser
Detaljeret beskrivelse
Background: This study is randomized clinical trial with double-blinded.
The aim is evaluate the effectiveness the training heavy with resistance exercise program in the muscle fatigue control.
Methods: This is a randomized controlled trial by cluster, in which workers who participate in the intervention group will perform resistance exercise protocols; and workers in the comparative group held only stretching exercises and light resistance training with elastic bands.
Expected results: strong evidence that fatigue reducing after ten weeks in workers and improve in others outcomes.
Not found in literature studies in occupational evaluating this aspect of training.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
352
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Espirito Santo
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Cachoeiro de Itapemirim, Espirito Santo, Brasilien, 29303300
- Centro Universitário São Camilo
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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:
- sign informed consent
Exclusion Criteria:
- restriction by the medical department.
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: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: Compensatory Workplace Exercise (CWE)
Comparative Group will receive a light training protocol including warming up, stretching and resisted exercise using elastic bands.
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The comparative group will receive warming up and stretching and light resisted exercise with elastic bands.
The exercise will realize three times per week, 20 minutes for day in total 60 minutes per week.
With warming up for 5 minutes and 15 minutes of the specific training .
The exercise will realize in 3 series with 10 repetitions and rest 30 seconds between series.
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Eksperimentel: Individual Resistance Exercise (IRE)
Intervention group will receive training protocol including warming up, stretching a specific resistance training with increase progressive load.
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Intervention group will receive warming up and stretching, and a specific resistance training with increase progress load.
The exercise will realize three times per week, 20 minutes for day in total 60 minutes per week.
With warming up and stretching for 5 minutes and 15 minutes of the specific training.
The exercise will realize in 3 series with 10 repetitions and rest 30 seconds between series.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Need for Recovery
Tidsramme: up to 4 months
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Psychosocial risk factors and stress, resulting in work-induced fatigue, will be obtained by e Need for Recovery Scale (NFR).
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up to 4 months
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Fatigue
Tidsramme: up to 4 months
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1 RM test is the maximum amount of weight lifted once while performing a standardized exercise for muscle groups - elbow , knee and ankle flexors and extensors, trunk.
A weight according to the maximum capacity is chosen.
If a replay is completed, find the value of 1RM.
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up to 4 months
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Musculoskeletal symptoms
Tidsramme: Outcome measures will be assessed at baseline and after 4 months.
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Musculoskeletal symptoms (pain, tingling or numbness) will be assessed using the Nordic Questionnaire for Musculoskeletal.
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Outcome measures will be assessed at baseline and after 4 months.
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Level of physical activity
Tidsramme: Outcome measures will be assessed at baseline and after 4 months.
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Questionnaire Baeck will be used to identify the level of habitual physical activity
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Outcome measures will be assessed at baseline and after 4 months.
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Perceived exposure
Tidsramme: Outcome measures will be assessed at baseline and after 4 months.
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The perception of workers risk factors that may contribute to the development of musculoskeletal complaints will be evaluated through the Job Factors Questionnaire.
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Outcome measures will be assessed at baseline and after 4 months.
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Physical Fitness Assessment
Tidsramme: Outcome measures will be assessed at baseline and after 4 months.
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The physical assessment will be consider adipometry (body fat percentage) others variables.
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Outcome measures will be assessed at baseline and after 4 months.
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Productivity
Tidsramme: Outcome measures will be assessed at baseline and after 4 months.
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Productivity is measured by a single item General Health Questionnaire and Performance at Work
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Outcome measures will be assessed at baseline and after 4 months.
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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: Rosimeire S Padula, Universidade Cidade de Sao Paulo
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Santos HG, Chiavegato LD, Valentim DP, Padula RS. Effectiveness of a progressive resistance exercise program for industrial workers during breaks on perceived fatigue control: a cluster randomized controlled trial. BMC Public Health. 2020 Jun 3;20(1):849. doi: 10.1186/s12889-020-08994-x.
- Santos HG, Chiavegato LD, Valentim DP, da Silva PR, Padula RS. Resistance training program for fatigue management in the workplace: exercise protocol in a cluster randomized controlled trial. BMC Public Health. 2016 Dec 22;16(1):1218. doi: 10.1186/s12889-016-3872-5.
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)
20. oktober 2015
Primær færdiggørelse (Faktiske)
12. december 2016
Studieafslutning (Faktiske)
3. marts 2017
Datoer for studieregistrering
Først indsendt
19. juni 2014
Først indsendt, der opfyldte QC-kriterier
23. juni 2014
Først opslået (Skøn)
24. juni 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
17. april 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
16. april 2019
Sidst verificeret
1. april 2019
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 454.709
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 .