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Hypo-hydration Mood and Cognition

10. mai 2019 oppdatert av: David Benton, Swansea University

Hypo-hydration, Mood and Cognition: the Effect of the Colour and Type of Drink

Recently changes in mood and cognition have been reported following minor reductions in hydration status. The aim is to explore that such changes in part at least reflect placebo response; therefore the consumption of plain or coloured water will be compared in drinks designed to differ in their ability to rehydrate.

Studieoversikt

Status

Ukjent

Intervensjon / Behandling

Detaljert beskrivelse

162 individuals will be subject to a temperature of 30°C for three hours, and mood and cognition monitored. Randomly on two occasions they will consume no drink or 300ml of plain or red colored water. In addition they will take a capsule containing sodium chloride or a placebo. Mood will be monitored using visual analogue scales and a battery of cognitive tests will be completed on three occasions: attention, episodic and working memory, reactions times. Urine osmolality will be measured at the beginning and end of the study and changes in body mass will be recorded. Changes in functioning will be related to the nature of the drink and changes in osmolality and body mass.

Studietype

Intervensjonell

Registrering (Forventet)

162

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

    • Wales
      • Swansea, Wales, Storbritannia, sa2 8pp
        • Rekruttering
        • Psychology, Swansea University
      • Swansea, Wales, Storbritannia, SA2 8PP
        • Rekruttering
        • Swansea University
        • Ta kontakt med:
        • 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 til 30 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion criteria:

  • 18 to 30 years
  • Non-smokers
  • BMI < 30
  • By self-report in good health
  • Not taking medication for any psychological or other health disorder.

Exclusion Criteria:

  • Do not meet inclusion criteria

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: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Sodium chloride / Water
300mg sodium chloride consumed in a capsule on two occasions with 300ml water
Drinks with and without a salt containing capsule
Aktiv komparator: Sodium chloride / no water
300 mg sodium chloride consumed
Drinks with and without a salt containing capsule
Aktiv komparator: Sodium chloride / colored water
300mg sodium chloride consumed in a capsule on two occasions with 300ml coloured water
Drinks with and without a salt containing capsule
Placebo komparator: Placebo / water
Placebo consumed in a capsule on two occasions with 300ml water
Drinks with and without a salt containing capsule
Placebo komparator: Placebo / no water
Placebo capsule consumed
Drinks with and without a salt containing capsule
Placebo komparator: Placebo / coloured water
Placebo consumed in a capsule on two occasions with 300ml colored water
Drinks with and without a salt containing capsule

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mood rating: agreeable / hostile
Tidsramme: Changes from baseline after 90 and 180 minutes
A hundred millimetre lines will be anchored with the words agreeable/hostile and the subject will rate their mood by marking the line.. My measuring in millimetres a score between 0 and 100 will result with a higher score indicating a more positive mood.
Changes from baseline after 90 and 180 minutes
Mood rating: confused / clearheaded
Tidsramme: Changes from baseline after 90 and 180 minutes
A hundred millimetre lines will be anchored with the words confused / clearheaded and the subject will rate their mood by marking the line.. My measuring in millimetres a score between 0 and 100 will result with a higher score indicating a more positive mood.
Changes from baseline after 90 and 180 minutes
Mood rating: composed / anxious
Tidsramme: Changes from baseline after 90 and 180 minutes
A hundred millimetre lines will be anchored with the words composed / anxious and the subject will rate their mood by marking the line.. My measuring in millimetres a score between 0 and 100 will result with a higher score indicating a more positive mood.
Changes from baseline after 90 and 180 minutes
Mood rating: depressed / elated
Tidsramme: Changes from baseline after 90 and 180 minutes
A hundred millimetre lines will be anchored with the words depressed / elated and the subject will rate their mood by marking the line.. My measuring in millimetres a score between 0 and 100 will result with a higher score indicating a more positive mood.
Changes from baseline after 90 and 180 minutes
Mood rating: tired / energetic
Tidsramme: Changes from baseline after 90 and 180 minutes
A hundred millimetre lines will be anchored with the words tired / energetic and the subject will rate their mood by marking the line.. My measuring in millimetres a score between 0 and 100 will result with a higher score indicating a more positive mood.
Changes from baseline after 90 and 180 minutes
Mood rating: confident / unsure
Tidsramme: Changes from baseline after 90 and 180 minutes
A hundred millimetre lines will be anchored with the words confident / unsure and the subject will rate their mood by marking the line.. My measuring in millimetres a score between 0 and 100 will result with a higher score indicating a more positive mood.
Changes from baseline after 90 and 180 minutes

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Episodic memory
Tidsramme: Changes from baseline after 90 and 180 minutes
A list of 30 words will be presented after which the subject writes down as many as can be recalled. The resulting score will vary from 0-30.
Changes from baseline after 90 and 180 minutes
Serial Sevens; test of working memory
Tidsramme: Changes from baseline after 90 and 180 minutes
28 numbers each of three digits will be presented and the subject indicates whether a subsequent number was exactly seven less. The measure reported is the response time in milli-seconds taken to respond
Changes from baseline after 90 and 180 minutes
Attention: Arrow Flankers
Tidsramme: Changes from baseline after 90 and 180 minutes
A series is presented that can be >>>>> or >><>> and the subject has to indicated whether the middle symbol points to the right or left. The measure reported is the time taken to respond in milli-seconds
Changes from baseline after 90 and 180 minutes
Reaction times
Tidsramme: Changes from baseline after 90 and 180 minutes
The time to press a button under an illuminated light was recorded in milli-seconds when there was 1, 2, 4, or 8 possible lamps that could be lit. 20 trials were performed with each of the four number of lights.
Changes from baseline after 90 and 180 minutes

Samarbeidspartnere og etterforskere

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

Etterforskere

  • Hovedetterforsker: David Benton, DSc, Professor of Psychology

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)

1. januar 2018

Primær fullføring (Forventet)

31. juli 2019

Studiet fullført (Forventet)

31. juli 2019

Datoer for studieregistrering

Først innsendt

8. mai 2019

Først innsendt som oppfylte QC-kriteriene

10. mai 2019

Først lagt ut (Faktiske)

13. mai 2019

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

13. mai 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

10. mai 2019

Sist bekreftet

1. mai 2019

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • DB-0519

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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. .

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