- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT01490034
Effects of Learning and Food Form on Intake in Humans
Due to the rising incidence of obesity, much emphasis has been placed on identifying mechanisms of increased energy intake. At this point, the mechanisms responsible for the recent increase in obesity prevalence have not been thoroughly examined. Pre-ingestive influences, such as cognitive factors, may play a larger role in creating an energy surplus than previously thought. Expectations about the satiating effect of a food may override the post-ingestive influences in dictating further consumption. In addition, obese individuals may exhibit a decreased compensatory response to foods as compared to lean individuals.
Understanding the effects of energy content, food form, and learning on satiation, satiety, and energy intake will allow for a greater understanding of the mechanisms of energy imbalance as a whole. Food choice is dictated by sensory properties and post-ingestive effects. By utilizing foods with similar sensory properties, the acquired knowledge derived from ingesting these foods can be monitored by analyzing subsequent intake at the same meal and at subsequent eating occurrences. It is hypothesized that the liquid food form will elicit weaker dietary compensation; that is, energy intake at other eating events will not be adjusted to compensate for that food. In addition, it is posited that the lower energy food will cause lower compensation postprandially. By having participants consume the same test food daily over a two week learning period, it is thought that they will show improved dietary compensation when the initial testing is repeated due to learned associations between food properties and metabolism.
Panoramica dello studio
Stato
Condizioni
Descrizione dettagliata
Tipo di studio
Iscrizione (Anticipato)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Indiana
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W. Lafayette, Indiana, Stati Uniti, 47907
- Purdue Univeristy
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Weight stable (<3 kg weight change within last 3 months)
- Constant habitual activity patterns (no deviation > 1x/wk at 30 min/session within last 3 months)
- Constant habitual diet patterns within last 3 months
- Willingness to eat a chocolate-flavored snack at test sessions and two week training period
- No allergies to any test foods
- Not planning to change use of medications known to influence appetite or metabolism
- Not diabetic
- No history of GI pathology
- Non-smoker for one year or more
Exclusion Criteria:
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Scienza basilare
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Energy dense beverage
Metabolic effects of consuming energy dense beverages before and after regular consumption
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Consumption of energy dense beverages for 2 weeks and monitoring physiological responses
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Sperimentale: Energy dense solid food form
Metabolic effects of consuming energy dense solid foods before and after regular exposure.
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Effects of consuming energy dense solid food for two weeks on physiological responses
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Sperimentale: Eenergy dilute beverages
Metabolic effects of consumption of energy dilute beverages on a regular basis.
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Effects of consuming energy dilute beverages for two weeks on physiological responses.
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Sperimentale: Energy dilute solid food form
Metabolic effects of consuming energy dilute sold foods before and after regular exposure.
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Effects of consuming energy dilute solid food for two weeks on physiological responses
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
energy intake
Lasso di tempo: 12 weeks
|
Energy consumed over 12 weeks of intervention.
|
12 weeks
|
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dietary compensation
Lasso di tempo: 12 weeks
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spontaneous dietary adjustment in response to intervention
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12 weeks
|
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appetite
Lasso di tempo: 12 weeks
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Effects of intervention on appetitive sensation such as hunger and fullness
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12 weeks
|
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effects of learning on energy intake
Lasso di tempo: 12 weeks
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The effects of learning based on exposure to products that are high or low in energy and liquid or solid
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12 weeks
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Effects of food form on energy intake
Lasso di tempo: 12 weeks
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The effects of food form on energy intake before and after chronic exposure to foods varying in food form and energy density
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12 weeks
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Effects of BMI on sensory learning
Lasso di tempo: 12 weeks
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The effects of BMI on appetite, energy intake and dietary compensation
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12 weeks
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Effects of personality traits on appetite, energy intake and compensation
Lasso di tempo: 12 weeks
|
Effects of personality traits related to feeding on appetite, energy intake and compensation following exposure to foods of different physical form, energy density and before and after learning.
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12 weeks
|
Collaboratori e investigatori
Sponsor
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- R01DK079913-3
- R01DK079913 (Sovvenzione/contratto NIH degli Stati Uniti)
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .