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Exercise at Workplace for Manual Material Handling Workers

16. april 2019 oppdatert av: Rosimeire Simprini Padula, Universidade Cidade de Sao Paulo

Effectiveness of Exercise at Workplace for Manual Material Handling Workers

This study aim to evaluate the effectiveness of exercise at workplace for manual material handling workers. This is a randomized control trial study by cluster with three parallel groups (n=200). Participants will be randomized in three groups: (1) control group - will be receive ergonomics orientation . (2) Intervention group - exercise at workplace four times per week, during 15 minutes; (3) Intervention group 2 - exercise at workplace three times per week, during 15 minutes.Outcomes: The outcome measure will be verified in three moments at baseline, in six and eleven months of the intervention. The primary outcome is pain, electromyography. Secondary outcome is palmar dynamometer, BMI, physical activity level.

Studieoversikt

Detaljert beskrivelse

Objective: This study aim to evaluate the effectiveness of exercise at workplace for control and prevention nonspecific low back pain. Methods: This is a randomized control trial study by cluster with three parallel groups. The context of this study is a motorcycle parts company importer localized in several states (Piaui, Ceará e Maranhão). The company has 575 workers, being 240 manual material handling. All are men over 18 years old that perform goods shipment (each work develop one this tasks - stock, separation, conference and packaging).

The inclusion criterial are workers that perform manual material handling for at least six months and signing informed consent form. The exclusion criterial were sick leave. The workers will be included with low back pain or no low back pain (at baseline). All will be interviewed to obtain: weight, height, BMI, age, marital status, educational level, and actual function (stock, separation, conference and packaging sick leave (the last 12 months), musculoskeletal complains, medications, complementary exams, surgery and or fractures. Participants will be randomized in three groups: (1) control group - will be receive orientation about manual material handling, postural and low back care (lecture and guidance). The training will be instructions according Ergonomics standard (NR17) about transportation and load handling and exercise in workout. (2) Intervention group 1 - will receive the same instruction of the control group, and will perform exercise at workplace four times per week, during 15 minutes; (3) Intervention group 2 - will be receive the same instruction of the control group, and will perform exercise at workplace three times per week, during 15 minutes. Outcomes: The outcome measure will be verified in three moments at baseline, six and eleven months of the intervention. The primary outcome is pain, electromyography. Secondary outcome is palmar dynamometer, BMI, exercise workout.

Expected Results: The manual material handling workers will be better after intervention by exercise at workplace. The effectiveness of exercise for low back pain and no low back pain groups will be contribute to change the behavior in occupational context.

Studietype

Intervensjonell

Registrering (Forventet)

240

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • São Paulo, Brasil, 12942770
        • Rekruttering
        • Rosimeire Simprini Padula
        • Ta kontakt med:

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

Mann

Beskrivelse

Inclusion Criteria:

  • The inclusion criterial are workers that perform manual material handling for at least six months and signing informed consent form.

Exclusion Criteria:

  • The exclusion criterial were sick leave

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: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Trippel

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Ingen inngripen: Control Group
The workers will be receive orientation about manual material handling, postural and low back care (lecture and guidance).
Aktiv komparator: Intervention group 1
The workers will be receive orientation about manual material handling, postural and low back care (lecture and guidance), and will perform exercise at workplace three times per week, during 15 minutes
The exercise at workplace will be occur during the workday during the rest breaks. The exercises perform are stretching, and using load.
Aktiv komparator: Intervention group 2
The workers will be receive orientation about manual material handling, postural and low back care (lecture and guidance) and and will perform exercise at workplace four times per week, during 15 minutes.
The exercise at workplace will be occur during the workday during the rest breaks. The exercises perform are stretching, and using load.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change from Pain Intensity at 6 months
Tidsramme: At baseline and after six months
Likert scale (0-10 points)
At baseline and after six months
Change from electromyographic signal at 6 months
Tidsramme: At baseline and after six months
RMS (root mean square error) signal and peak signal by Electromyographic (EMG)
At baseline and after six months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change from palmar grip strength at 6 months
Tidsramme: At baseline and six months
Three measure palmar grip strength to use the mean by dynamometer
At baseline and six months
Change from body mass index at 6 months
Tidsramme: At baseline and after six months
The body mass index will be calculated on height divided by square weight
At baseline and after six months
Change of behavior to exercise
Tidsramme: At baseline and after six months
Practice of exercise (practice - yes or no; number of times per week)
At baseline and after six months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

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)

25. juli 2018

Primær fullføring (Faktiske)

19. desember 2018

Studiet fullført (Forventet)

17. desember 2020

Datoer for studieregistrering

Først innsendt

29. april 2018

Først innsendt som oppfylte QC-kriteriene

20. juli 2018

Først lagt ut (Faktiske)

24. juli 2018

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

17. april 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

16. april 2019

Sist bekreftet

1. april 2019

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 2.372.435

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