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Effect of Kinesiotaping on Force Irradiation

7. september 2018 oppdatert av: Bezmialem Vakif University

The Determination of Relationship Between Kinesiotaping and Contralateral Force Irradiation

The study is assessed the electromyographic activity response of non-dominant biceps brachii muscle during unilateral-dominant concentric, eccentric and isometric biceps brachii muscle contractions under kinesiotaping and non-taping conditions. The aim of the study is to determine the synergistic effect of kinesiotaping which is applied on non-dominant biceps brachii muscle on force irradiation.

Studieoversikt

Status

Fullført

Forhold

Detaljert beskrivelse

Fourty healthy subjects with no history of neurological or recent musculoskeletal injury will participate the study.

Healthy subjects are arranged in two groups of stimulation: kinesiotaping group (kinesiotaping and force irradiation) and control group (only force irradiation). The electromyographic response of the resting arm (non-dominant) will be assessed during the dominant arm movement for all subjects. Additionally, in kinesiotaping group, kinesiotaping will be applied 24 hours before the experiment.

The electromyographic response of the resting arm will be assessed under three contraction type movement (isometric, eccentric and concentric contractions) The SEMG signals are analysed by using MATLAB®, suitable signal proccessing techniques (linear envelope, Root Mean Square etc) are chosed. The statistical analysis are done by using SPSS®, according to data distribution, "Independent Sample T Test" or "Mann-Whitney U Test" is utilized for comparing outcomes of control and KT groups.

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

      • Istanbul, Tyrkia
        • Bezmialem Vakıf University

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 30 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • To be right-handed-dominant
  • To have normal or corrected vision
  • To have no formal history of any resistance training.

Exclusion Criteria:

  • To have history of neurological or recent musculoskeletal injury

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Kinesiotaping Group
The group in which kinesiotaping is applied to non-dominant biceps brachii muscle of participants before 24 hours the force irradiation experiment.
For the force irradiation, while the subjects perform dominant elbow flexion at an angular velocity of 60°/s for concentric contractions, 30°/s for eccentric contractions, at 90° elbow flexion position for isometric contractions with a maximal effort level, electrical activity of the non-dominant biceps brachii and triceps brachii muscles are recorded.
For kinesiotaping, the elbow positioned in 30°-45° flexion and kinesiotaping facilitation technique is applied origin to insertion of non-dominant biceps brachii muscle before 24 hours the experiment.
Andre navn:
  • Force Irradiation
Aktiv komparator: Control group
The group in which the participants only perform the the force irradiation experiment.
For the force irradiation, while the subjects perform dominant elbow flexion at an angular velocity of 60°/s for concentric contractions, 30°/s for eccentric contractions, at 90° elbow flexion position for isometric contractions with a maximal effort level, electrical activity of the non-dominant biceps brachii and triceps brachii muscles are recorded.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Measurement of the surface electromyographic activity of left biceps brachii muscle by using surface electromyography device while the right elbow performs isometric elbow flexion
Tidsramme: after inclusion
while the right elbow performs isometric elbow flexion, electromyographic activity of left biceps brachii was determined by using surface electromyography device. After signal processing and normalization, the electromyographic data of kinesiotaping and control groups will be compared.
after inclusion
Measurement of the surface electromyographic activity of left triceps brachii muscle by using surface electromyography device while the right elbow performs isometric elbow flexion
Tidsramme: after inclusion
while the right elbow performs isometric elbow flexion, electromyographic activity of left triceps brachii was determined by using surface electromyography device. After signal processing and normalization, the electromyographic data of kinesiotaping and control groups will be compared.
after inclusion
Measurement of the surface electromyographic activity of left biceps brachii muscle by using surface electromyography device while the right elbow performs concentric elbow flexion.
Tidsramme: after inclusion
while the right elbow performs concentric elbow flexion, electromyographic activity of left biceps brachii was determined by using surface electromyography device. After signal processing and normalization, the electromyographic data of kinesiotaping and control groups will be compared.
after inclusion
Measurement of the surface electromyographic activity of left triceps brachii muscle by using surface electromyography device while the right elbow performs concentric elbow flexion
Tidsramme: after inclusion
while the right elbow performs isometric elbow flexion, electromyographic activity of left triceps brachii was determined by using surface electromyography device. After signal processing and normalization, the electromyographic data of kinesiotaping and control groups will be compared.
after inclusion
Measurement of the surface electromyographic activity of left biceps brachii muscle by using surface electromyography device while the right elbow performs eccentric elbow flexion
Tidsramme: after inclusion
while the right elbow performs eccentric elbow flexion, electromyographic activity of left biceps brachii was determined by using surface electromyography device. After signal processing and normalization, the electromyographic data of kinesiotaping and control groups will be compared.
after inclusion
Measurement of the surface electromyographic activity of left triceps brachii muscle by using surface electromyography device while the right elbow performs eccentric elbow flexion
Tidsramme: after inclusion
while the right elbow performs eccentric elbow flexion, electromyographic activity of left triceps brachii was determined by using surface electromyography device. After signal processing and normalization, the electromyographic data of kinesiotaping and control groups will be compared.
after inclusion

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Measurement of the electromyographic activity of left biceps brachii muscle during left elbow maximum isometric flexion by using electromyography device.
Tidsramme: after inclusion
Electromyographic activity of left elbow maximum isometric flexion is used for normalizing force irradiation data of left biceps brachii muscle
after inclusion
Measurement of the electromyographic activity of left triceps brachii muscle during left elbow maximum isometric extension by using electromyography device.
Tidsramme: after inclusion
Electromyographic activity of left elbow maximum isometric extension is used for normalizing force irradiation data of left triceps brachii muscle
after inclusion

Samarbeidspartnere og etterforskere

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

Samarbeidspartnere

Etterforskere

  • Studieleder: Aydın AKAN, Istanbul University

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)

10. august 2017

Primær fullføring (Faktiske)

20. mai 2018

Studiet fullført (Faktiske)

3. september 2018

Datoer for studieregistrering

Først innsendt

6. februar 2018

Først innsendt som oppfylte QC-kriteriene

19. mars 2018

Først lagt ut (Faktiske)

20. mars 2018

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. september 2018

Siste oppdatering sendt inn som oppfylte QC-kriteriene

7. september 2018

Sist bekreftet

1. september 2018

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • hdenizkulli

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Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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