- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03103048
Application of Different Techniques of Elastic Bandage
17. mai 2018 oppdatert av: Terigi Augusto Scardovelli, University of Mogi das Cruzes
Application of Different Techniques of Elastic Bandage: Quantification Electromyographic at the Isometric Effort of Flexor Muscle of Fist
This study will be featured as a randomized controlled.
As the dependent variable, was considered isometric grip manual force.
As independent variable, the presence or absence of forearm bandage in the fist flexor region of the volunteers.
Studieoversikt
Status
Fullført
Forhold
Detaljert beskrivelse
This study is directed to the population of students at the University of Mogi das Cruzes (UMC), and will take part of this study forty volunteers, twenty men and twenty women, aged from eighteen and thirty-eight years old.
Will be selected and included volunteers who do not do physical professional activity with upper members, which have no symptom of pain skeletal muscle in the upper members, which have not undergone any type of surgery in the region of the forearm and hand of both members.
Will be excluded the volunteers who have injuries, joint injuries, neuromuscular disorder or those who have knowledge of own vestibular or neurological changes.
Will also be excluded from study volunteers who do not agree to participate after reading and understanding of informed consent in accordance with resolution 466/12 of the National Ethics Committee and Research.
The data acquisition interface will be acquired by an electromyography e a standard of strentgh will maintened in forty Newtons assured by an electronic dynamometer for tests of palmar prehension without and with bandages.
The volunteers will not know what kind of intervention will pass.
After each application before testing, their both forearms will be covered with a protection.
The researcher and the volunteers will not know the tests order.
Studietype
Intervensjonell
Registrering (Faktiske)
40
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
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São Paulo
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Mogi Das Cruzes, São Paulo, Brasil, 08615120
- Terigi Augusto Scardovelli
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-
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 til 38 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Who do not do physical professional activity with upper members;
- Who have no symptom of pain skeletal muscle in the upper members;
- Who have not undergone any type of surgery in the region of the forearm and hand of both members;
- Consent form signed by the volunteer.
Exclusion Criteria:
- Having less than 18 years old;
- Having more than 38 years old;
- To present some compromise skeletal muscle in the upper members;
- Who do not want take part in the research;
- Who do not signed consent form as volunteer.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Diagnostisk
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Dobbelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Aktiv komparator: Group 1
The tests will be performed in thirty days, session with lasting 15 minutes each, when all volunteers will be submitted in four measure tests: 1- Without bandages (start); 2 - With placebo; 3 - With bandage; 4 - With tensioned bandage.
|
All volunteers will be held the grasping force measurements without application of elastic adhesive bandage or micropore
All volunteers will be held the grasping force measurements with application of micropore (placebo) on his forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage without tension in the forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage with twenty five percent tensioned on the forearm in both upper members
|
Placebo komparator: Group 2
The tests will be performed in thirty days, session with lasting 15 minutes each, when all volunteers will be submitted in four measure tests: 1- Without bandages; 2 - With placebo (start); 3 - With bandage; 4 - With tensioned bandage.
|
All volunteers will be held the grasping force measurements without application of elastic adhesive bandage or micropore
All volunteers will be held the grasping force measurements with application of micropore (placebo) on his forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage without tension in the forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage with twenty five percent tensioned on the forearm in both upper members
|
Aktiv komparator: Group 3
The tests will be performed in thirty days, session with lasting 15 minutes each, when all volunteers will be submitted in four measure tests: 1- Without bandages; 2 - With placebo; 3 - With bandage (start); 4 - With tensioned bandage.
|
All volunteers will be held the grasping force measurements without application of elastic adhesive bandage or micropore
All volunteers will be held the grasping force measurements with application of micropore (placebo) on his forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage without tension in the forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage with twenty five percent tensioned on the forearm in both upper members
|
Aktiv komparator: Group 4
The tests will be performed in thirty days, session with lasting 15 minutes each, when all volunteers will be submitted in four measure tests: 1- Without bandages; 2 - With placebo; 3 - With bandage; 4 - With tensioned bandage (start).
|
All volunteers will be held the grasping force measurements without application of elastic adhesive bandage or micropore
All volunteers will be held the grasping force measurements with application of micropore (placebo) on his forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage without tension in the forearm in both upper members
All volunteers will be held the grasping force measurements with application of bandage with twenty five percent tensioned on the forearm in both upper members
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Efforts
Tidsramme: 15 minutes
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Thru palmar prehension there will be data acquisition interface by an electromyography e a standard of strentgh maintened in 40 Newtons assured by an electronic dynamometer for tests of palmar prehension, with and without elastic adhesive bandages in the region of flexor muscle of fist.
|
15 minutes
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Terigi A Scardovelli, Ph.D., University of Mogi das Cruzes
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)
3. april 2017
Primær fullføring (Faktiske)
8. mai 2017
Studiet fullført (Faktiske)
21. juni 2017
Datoer for studieregistrering
Først innsendt
31. mars 2017
Først innsendt som oppfylte QC-kriteriene
31. mars 2017
Først lagt ut (Faktiske)
6. april 2017
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
18. mai 2018
Siste oppdatering sendt inn som oppfylte QC-kriteriene
17. mai 2018
Sist bekreftet
1. april 2017
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- CAAE 64513617.3.0000.5497
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
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Nei
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