Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Melatonin Supplementation and Performance (MSP)

18. august 2016 oppdatert av: kais

Nocturnal Melatonin Ingestion Ameliorates Short Term Maximal Performances on the Following Day

The present study aimed to evaluate the possible effect of nocturnal melatonin ingestion upon short-term performances, on the following morning. Twelve soccer players from a Tunisian squad (22.9 ±1.3 years, 1.80±0.05 m, and 72.0±8.8 kg) were volunteered to perform three testing sessions, with one test session per day. During each session, MEL (5mg) , MEL (8mg) or placebo were ingested, in a randomized order, before nocturnal sleep. The next morning (08:00h), participants performed the following psycho-cognitive and physical tests: Hooper's index, reaction time, vigilance, handgrip strength , squat jump , modified agility test , Wingate anaerobic test (peak power , mean power and fatigue index ). Rating of perceived exertion was recorded immediately after the WanT, and blood lactate measures were taken after 3min of recovery. Blood glucose was measured before and 3 min after the Wingate test.

Studieoversikt

Studietype

Intervensjonell

Registrering (Faktiske)

12

Fase

  • Tidlig fase 1

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

20 år til 23 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

Inclusion Criteria:

The participants were recruited based on the following criteria: (i) paticipants must be trained at 4-6 days per week for an average of 2 h daily and (ii) they must have at least 8 years of training experience

Exclusion Criteria:

  • Subjects were excluded from the study if they present one of the following criteria : heart failure, antioxidant supplementation within 3 months before the study, lower-limb injuries

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Grunnvitenskap
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: Placebo
In a double-blind randomized design, participants have taken placebo supplementation in one of the three experimental sessions
Eksperimentell: Melatonin
Our protocol was composed of three experimental sessions. During each testing session, participants were requested to attend the laboratory at 20:00h where they ingested a standardized light meal. Melatonin (5 mg or 8 mg) or placebo were ingested in capsule in the evening at 21:00h in a double-blind randomized design

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Hooper's index score
Tidsramme: At 07:30 am in the following day of the supplementation
Hooper's index score was measured using a specific questionnaire
At 07:30 am in the following day of the supplementation
handgrip strength (in Kg)
Tidsramme: At 07:30 am in the following day of the supplementation
handgrip strength was measured using a calibrated hand dynamometer.
At 07:30 am in the following day of the supplementation
Blood lactate (µmol/l)
Tidsramme: Blood lactate was measured only 3 minutes after physical testing in the following day of the supplementation
Lactate level was measured using Lactate Pro instrument.
Blood lactate was measured only 3 minutes after physical testing in the following day of the supplementation
reaction time (in secondes)
Tidsramme: At 07:30 am in the following day of the supplementation
Reaction time was measured using an electronic timing device.
At 07:30 am in the following day of the supplementation
vigilance score
Tidsramme: At 07:30 am in the following day of the supplementation
Vigilance score was measured using a specific questionnaire
At 07:30 am in the following day of the supplementation
squat jump (in centimeters)
Tidsramme: At 07:30 am in the following day of the supplementation
Squat jump was assessed using a infrared jump system
At 07:30 am in the following day of the supplementation
agility (in secondes)
Tidsramme: At 07:30 am in the following day of the supplementation
Agility was assessed using an electronic timing system.
At 07:30 am in the following day of the supplementation
anaerobic capacity (In watts)
Tidsramme: At 07:30 am in the following day of the supplementation
Anaerobic capacity was assessed using a calibrated friction-loaded cycle ergometer
At 07:30 am in the following day of the supplementation
glucose level (µmol/l)
Tidsramme: At 07:30 am in the following day of the supplementation (rest condition) and 3 minutes after physical testing in each experimental session
Glucose level was assessed using a glucometer
At 07:30 am in the following day of the supplementation (rest condition) and 3 minutes after physical testing in each experimental session
Rating of perceived exertion score
Tidsramme: Rating of perceived exertion score was measured 3 minutes after physical testing in the following day of the supplementation
Rating of perceived exertion score was measured using a specific questionnaire
Rating of perceived exertion score was measured 3 minutes after physical testing in the following day of the supplementation

Samarbeidspartnere og etterforskere

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

Sponsor

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

1. desember 2012

Primær fullføring (Faktiske)

1. januar 2013

Studiet fullført (Faktiske)

1. januar 2013

Datoer for studieregistrering

Først innsendt

2. august 2016

Først innsendt som oppfylte QC-kriteriene

18. august 2016

Først lagt ut (Anslag)

24. august 2016

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

24. august 2016

Siste oppdatering sendt inn som oppfylte QC-kriteriene

18. august 2016

Sist bekreftet

1. august 2016

Mer informasjon

Begreper knyttet til denne studien

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere