Very Low Calorie Diet Weight Loss
3 febbraio 2022 aggiornato da: Marielle PKJ Engelen, PhD, Texas A&M University
Omics Profiling of the Response to Food and Variability of Weight Loss in Medically Supervised Very Low Calorie Diet
Understanding how foods and nutrients are digested, absorbed and metabolized when weight is stable and during weight loss induced by very low calorie diet procedure using the technologies of genomics, transcriptomics, proteomics, metabolomics and fluxomics ("omics") will enable generation of new hypotheses that could explain the inter-individual differences in weight loss and could lead to optimization and individualization of therapies designed to lose weight.
Panoramica dello studio
Stato
Completato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
The overarching hypothesis is that there are baseline, pre- and post-diet combinations of 'omics' signatures in response to food and nutrients that explain the weight loss response of obese subjects to the very low calorie (VLC) diet.
In order to address the general hypothesis the following specific aims will be addressed:
Specific Aim 1: To test the hypothesis that there is a combination of 'omics' parameters in response to a defined meal that discriminate between morbidly obese subjects.
Specific Aim 2: To test the hypothesis that variation in % weight loss to the 2-weeks of VLC diet is related to baseline genomic markers, gene expression profile, proteomic and metabolomic signatures as well as baseline metabolic and substrates fluxomics response to a defined meal.
Specific Aim 3: To test the hypothesis that variation in % weight loss to the 4-weeks of VLC diet is related to baseline genomic markers, gene expression profile, proteomic and metabolomic signatures as well as baseline metabolic and substrates fluxomics response to a defined meal.
Tipo di studio
Interventistico
Iscrizione (Effettivo)
56
Fase
- Non applicabile
Contatti e Sedi
Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.
Luoghi di studio
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Texas
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College Station, Texas, Stati Uniti, 77843
- Texas A&M University-CTRAL
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Criteri di partecipazione
I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.
Criteri di ammissibilità
Età idonea allo studio
30 anni e precedenti (Adulto, Adulto più anziano)
Accetta volontari sani
No
Sessi ammissibili allo studio
Tutto
Descrizione
Inclusion criteria obese subjects:
Diagnosed with morbid obesity (defined as BMI > 40 kg/m2 or BMI > 35 kg/m2 with at least one serious comorbidity (2013 NIH compendium guidelines)) Scheduled for medically supervised Very Low Calorie Diet Age 30 years and older Ability to lay in supine or elevated position for 5 hours Willingness and ability to comply with the protocol Exclusion Criteria Any condition that may interfere with the definition 'healthy subject' according to the investigator's judgment (for healthy control group only) Participation in Weight Loss Management Program within the last 6 months prior the first study day Presence of fever within the last 3 days Untreated metabolic diseases including hepatic or renal disorder unrelated to the primary disease Presence of acute illness or metabolically unstable chronic illness unrelated to the primary disease
· (Possible) pregnancy Any other condition according to the PI or nurse that would interfere with the study or safety of the patient Failure to give informed consent Use of protein or amino acid containing nutritional supplements within 3 days of first test day
Piano di studio
Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Terapia di supporto
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: obese
screening visit: body weight and composition by DXA, height, and vital signs will be assessed. Subjects may sign a medical release form to obtain medical and psychological information about them that will help determine study eligibility or can be used for later coding. 3 study days (one baseline, one approx 2 weeks of diet, one post-diet): muscle mass and function tests, resting energy expenditure, stable isotope infusions with blood draws, and questionnaires regarding quality of life, mood and depression, diet. |
come glicerolo, D2O, tirosina, fenilalanina, glucosio, arginina e citrullina
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
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Variazione della sintesi proteica netta dell'intero corpo
Lasso di tempo: 0, 2, 5, 10, 15, 20, 30, 40, 50, 60, 90, 120, 150, 180, 210, 225, 240, 260, 280, 300, 320, 340, 360 ± 5 min
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Variazione del tasso di sintesi proteica di tutto il corpo dopo l'assunzione di un pasto
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0, 2, 5, 10, 15, 20, 30, 40, 50, 60, 90, 120, 150, 180, 210, 225, 240, 260, 280, 300, 320, 340, 360 ± 5 min
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Group differences in state of mood as measured by the Hospital Anxiety and Depression Scale (HADS)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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a fourteen item self-assessment scale.
Seven of the items related to anxiety and seven relate to depression.
Each item on the questionnaire is scored from 0-3 and this means that a person can score between 0 (no symptoms) and 21 (severe symptoms) for either anxiety or depression.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Executive Function-Adolescent/Adult Sensory Profile (ASP)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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a standardized self-questionnaire that generates an individualized profile of sensory processing across four quadrants: low registration, sensation seeking, sensory sensitivity, and sensation avoiding.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in quality of life as measured by Short Form (36) Health Survey (SF36)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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self administered questionnaire that measures each of the following eight health concepts: Physical Functioning (PF); Role-Physical (RP); Bodily Pain (BP); General Health (GH); Vitality (VT); Social Functioning (SF); Role-Emotional (RE); Mental Health (MH) as well as a reported Health Transition item (HT)
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in activity as measured by Physical Activity Scale for the Elderly (PASE)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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questionnaire is intended for use in an elderly population and focuses on 3 types of activities: leisure time activities, household activities and work-related activities.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in attention and executive functions as measured by Stroop Color-Word Test (SCWT)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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a word page with words printed in black ink, a color page with blocks printed in color, and a color-word page where the color and the word do not match.
The examinee reads the words or names the ink colors as quickly as possible within a time limit.
Measures selective attention and inhibitory control.
The total time in seconds was reported for each trial.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in state of mood as measured by the Profile of Mood State (POMS)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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A psychological distress scale to measure mood disturbance in 6 domains - fatigue-inertia, vigor-activity, tension-anxiety, depression-dejection, anger-hostility, and confusion-bewilderment.
Healthy populations take 3 to 7 minutes to complete, and others may take up a bit longer.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in learning and memory as measured by Controlled Oral Word Association Test (COWAT)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Controlled Oral Word Association Test (COWAT): The examinee is required to say as many words as they can think of in one minute that begin with a given letter of the alphabet.
The task contains three trials.
Measures phonetic verbal fluency.
The raw score (total and mean words recorded across the three trials) was reported.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in learning and memory as measured by Auditory Verbal Learning Test (AVLT)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Auditory Verbal Learning Test (AVLT): a verbal episodic memory test that evaluates a wide diversity of functions: short-term auditory-verbal memory, rate of learning, retention and recognition of information
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in attention and executive functions as measured by PASAT
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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a measure of cognitive function that assesses auditory information processing speed and flexibility, as well as calculation ability.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in attention and executive functions as measured by Trail Making Test (TMT)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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In Part A, the examinee is instructed to connect a set of 25 circles with numbers as quickly as possible while maintaining accuracy.
In Part B, the examinee is instructed to connect a set of 25 circles, alternating between numbers and letters, as quickly as possible while maintaining accuracy.
Measures attentional resources and is a measure of the frontal lobe "executive" functions of visual search, set-switching and mental flexibility.
The total time in seconds was reported for each measure.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in overall cognitive abilities as measured by Montreal Cognitive Assessment (MoCA)
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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assesses several cognitive domains and is used for the screening of mild cognitive impairment.
Total scores range from 0-30 with lower scores indicating decreased functioning.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Group differences in attention and executive functions as measured by Brief-A
Lasso di tempo: Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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a standardized self-report that captures views of an adult's executive functions or self-regulation in his or her everyday environment.
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Postabsorptive state during 3 hours and change after feeding on study day 1 and the change from day 2 and day 3
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Skeletal muscle strength
Lasso di tempo: on study day 1 and the change from day 2 and day 3
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handgrip and kin-com 1-leg test
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on study day 1 and the change from day 2 and day 3
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24 hour diet recall
Lasso di tempo: on study day 1 and the change from day 2 and day 3
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The subject is asked to recall in detail all the food and drink consumed during the 24 hours prior to the test day.
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on study day 1 and the change from day 2 and day 3
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Respiratory muscle strength
Lasso di tempo: on study day 1 and the change from day 2 and day 3
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Maximum inhalation and exhalation pressure
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on study day 1 and the change from day 2 and day 3
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Body Composition
Lasso di tempo: on study day 1 and the change from day 2 and day 3
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Body composition as measured by Dual-Energy X-ray Absorptiometry on study day 1 and the change from day 2 and day 3
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on study day 1 and the change from day 2 and day 3
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Gut function
Lasso di tempo: postabsorptive and prandial state every 20 minutes up to 6 hours before each sip feeding on day 1 and the change from day 2 and day 3
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Digestion of the stable tracers of amino acid
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postabsorptive and prandial state every 20 minutes up to 6 hours before each sip feeding on day 1 and the change from day 2 and day 3
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Collaboratori e investigatori
Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.
Sponsor
Investigatori
- Investigatore principale: Marielle Engelen, Texas A&M University
Pubblicazioni e link utili
La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.
Studiare le date dei record
Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.
Studia le date principali
Inizio studio (Effettivo)
1 maggio 2016
Completamento primario (Effettivo)
1 ottobre 2018
Completamento dello studio (Effettivo)
1 ottobre 2018
Date di iscrizione allo studio
Primo inviato
19 maggio 2016
Primo inviato che soddisfa i criteri di controllo qualità
19 maggio 2016
Primo Inserito (Stima)
23 maggio 2016
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
4 febbraio 2022
Ultimo aggiornamento inviato che soddisfa i criteri QC
3 febbraio 2022
Ultimo verificato
1 febbraio 2022
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- IRB2016-0304
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
No
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 .
Prove cliniche su Infusione di aminoacidi isotopici stabili
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Central Hospital, Nancy, FranceNon ancora reclutamento