- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01544816
Evaluating the Effects of Snack Products on Energy
6. maj 2013 opdateret af: Mondelēz International, Inc.
To determine the effect of snack products varying in composition, on energy in healthy adult subjects.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
49
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Georgia
-
Atlanta, Georgia, Forenede Stater, 30341
- Mercer University Center for Clinical Research
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
20 år til 45 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- The subject must provide informed consent.
- The subject is male or female, and between the ages of 20 and 45, inclusive.
- The subject is a routine, moderate daily user of caffeine (approximately 1-4 cups of coffee or equivalent).
- The subject is fluent in English.
- The subject has a minimum of a high school diploma.
- Females of Child-bearing Potential (FOCP) must have a negative urine or serum beta HCG pregnancy test at screening. FOCP must abstain from sexual activity that could result in a pregnancy, or use acceptable contraceptives throughout the period of study treatment exposure. Acceptable contraceptives include IUDs, hormonal contraceptives (oral, implanted or injectable) and double barrier methods (such as condom or diaphragm with spermicidal gel). If hormonal contraceptives are used, the period of use must be sufficiently long to achieve pharmacological effectiveness prior to study treatment exposure (refer to individual product information for details on onset of effectiveness). FOCP who are not currently sexually active, must agree to use acceptable contraception, as defined above, if they decide to become sexually active during the period of study treatment exposure .
- The subject is in good physical and mental health based on a general medical history.
- The subject has adequate visual and auditory acuity and cognitive ability to complete the assessments and is capable of understanding and following instructions for the performance tests within the normal, age-adjusted range (within one SD) at screening.
- Must be able and willing to obtain a minimum of 7 hours of sleep the night prior to each study visit.
- The subject is willing and able to comply with all requirements defined within this protocol.
- The subject reports having a snack at least two afternoons per week.
- The subject reports experiencing an "afternoon slump".
Exclusion Criteria
- The subject has a current Axis I or Axis II comorbid psychiatric diagnosis or other symptomatic manifestations that, in the opinion of the examining physician (Investigator), will contraindicate treatment with caffeine.
- Attention Deficit Disorder or Attention Deficit Hyperactivity Disorder
- BMI ≤ 19 or ≥ 30 kg/m2.
- The subject has documented allergies, adverse reactions, or intolerance to caffeine.
- The subject has any significant medical illness or condition for which caffeine is contraindicated.
- The subject has a history of drug dependence or substance use disorder based upon DSM-IV-TR criteria (excluding nicotine).
- The subject has a positive urine drug or alcohol drug test result (to include nicotine).
- The subject has participated in an investigational study or received an investigational drug within the past 28 days.
- The subject has used nicotine products within 30 days of screening or during the duration of the study.
- The subject is taking medications, that have CNS effects or affect performance, (such as sedating antihistamines and decongestant sympathomimetics, either oral or topical), and may interfere with efficacy or safety assessments.
- The subject has a concurrent chronic or acute illness (such as allergic rhinitis or severe cold), disability, or other condition that might confound the results of rating tests administered in the study or that might increase risk to the subject. Similarly, the subject will be excluded if he or she has any additional conditions that, in the Investigator's opinion, would preclude the subject from completing the study or would not be in the best interest of the subject. This would include any significant illness or unstable medical condition that could lead to difficulty complying with the protocol.
- The female subject is pregnant or lactating or planning on becoming pregnant during the study
- Hypertension or other chronic medical conditions
- Individuals who do not maintain a routine nighttime sleep schedule (e.g. no shift work).
- Individuals judged by the Investigator to be unsuitable for enrollment in this study for any reason.
- The subject has been diagnosed with phenylketonuria.
- Inability to perform performance tests within the Normal range (i.e., performance no lower than 1SD below the mean) at screening.
- The subject has a pre-existing medical condition.
- Subject has been diagnosed with a sleeping disorder.
- Subject has a fasting glucose of >110 mg/dl.
- Subject has an allergy to wheat, soy, nuts or other food.
- Subject has Kosher or Halal dietary restrictions.
- Subject reports never eating biscuits, cookies or crackers.
- Epworth Sleepiness Scale ≥ at screening (i.e., evidence of excessive daytime sleepiness).
- Dislike of chocolate flavorings
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Placebo komparator: Control Food Product
Control food product
|
control food product
Experimental food product containing ingredient 1
Experimental food product containing ingredient 2
|
Eksperimentel: Experimental Food Product 1
Experimental food product 1
|
control food product
Experimental food product containing ingredient 1
Experimental food product containing ingredient 2
|
Eksperimentel: Experimental Food Product 2
Experimental food product 2
|
control food product
Experimental food product containing ingredient 1
Experimental food product containing ingredient 2
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Energy questionnaire OR Rating of perceived energy OR Subjective feeling of energy (visual analog scale)
Tidsramme: 90 minutes post snack
|
90 minutes post snack
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Chad VanDenBerg, Pharm.D., Mercer University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. februar 2012
Primær færdiggørelse (Faktiske)
1. august 2012
Studieafslutning (Faktiske)
1. august 2012
Datoer for studieregistrering
Først indsendt
24. februar 2012
Først indsendt, der opfyldte QC-kriterier
29. februar 2012
Først opslået (Skøn)
6. marts 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
8. maj 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
6. maj 2013
Sidst verificeret
1. maj 2013
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- KFG-123X-01
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Energi
-
University of ReadingBiotechnology and Biological Sciences Research Council; The Norwegian Institute... og andre samarbejdspartnereIkke rekrutterer endnuProtein-Energy UnderernæringDet Forenede Kongerige
-
Hospital General Universitario Gregorio MarañonInstituto de Salud Carlos III; European Regional Development Fund; Maternal...UkendtProtein-Energy UnderernæringSpanien
-
Assistance Publique - Hôpitaux de ParisAfsluttetProtein-Energy UnderernæringFrankrig
-
An Hsin QingShui ClinicAfsluttet
-
Semarang Health PolytechnicUkendtAnæmi | Graviditet | Protein-Energy UnderernæringIndonesien
-
Seoul St. Mary's HospitalAfsluttetProtein-Energy UnderernæringKorea, Republikken
-
University of FloridaAktiv, ikke rekrutterendeNyresvigt | Protein-Energy UnderernæringForenede Stater
-
VU University of AmsterdamAmsterdam UMC, location VUmc; University of HelsinkiAfsluttetFysisk handicap | Protein-Energy UnderernæringFinland, Holland
-
Action Contre la FaimJohns Hopkins UniversityUkendt
-
United States Army Research Institute of Environmental...RekrutteringStress, Fysiologisk | Energiforsyning; Mangel | Energiforsyning; Mangel, AlvorligForenede Stater
Kliniske forsøg med Snack Product
-
Radicle ScienceAktiv, ikke rekrutterendeKognitiv funktionForenede Stater
-
Penn State UniversityRekruttering
-
Ryerson UniversityThe Hershey CompanyAfsluttetFødeindtagelse | MæthedCanada
-
Radicle ScienceRekrutteringSmerte | Neuropatisk smerte | Nociceptiv smerteForenede Stater
-
Mondelēz International, Inc.Reading Scientific Services Ltd.Afsluttet
-
USDA, Western Human Nutrition Research CenterAlmond Board of CaliforniaAfsluttet
-
University of FloridaFresenius Medical Care North America; National Kidney FoundationAfsluttetNyresvigt | Kostvane | Albumin; DobbeltForenede Stater
-
USDA Beltsville Human Nutrition Research CenterAfsluttet
-
University of Colorado, DenverAmerican Pecan CouncilAfsluttetOvervægt og fedmeForenede Stater