- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT04527952
The Fasting and Shifted Timing (FAST) of Eating Study (FAST)
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Fasting and time-restricted feeding (TRF) have become increasingly popular in nutrition research due to the potential health benefits they may provide. Several animal studies, and more recently some human studies, have indicated regular meal-timing (i.e. eating mostly in the day) or fasting have been beneficial for controlling weight, blood pressure, cholesterol, glucose, and insulin sensitivity.
These types of eating patterns may offer the same "anti-aging" health benefits as traditional caloric restriction (i.e. consistent and routine adherence to a very low-calorie diet).While caloric restriction is considered the gold standard for weight management, weight regain often limits the long-term effectiveness of this approach. People often experience increases in hunger, which make it difficult to sustain this type of behavior.Therefore, researchers are turning to these dietary approaches as alternatives to low-calorie diets in an effort to obtain the same benefits, but with less burden on participants.
However, it is not clear if the adherence to these types of diet protocols are any better than a low-calorie diet. Would people be more satisfied with meal-timing or fasting over a traditional very low-calorie diet? That is the main research question of this study.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
South Carolina
-
Columbia, South Carolina, États-Unis, 29208
- University of South Carolina
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Be 18 years or older.
- Have a BMI between 25 - 49.9 kg/m2.
- Have a scale at home, or some way of weighing yourself regularly, so that you can report your body weight to the research staff.
- Be able to check emails regularly, because all of the surveys need to be completed online.
Exclusion Criteria:
- NOT be already practicing any of these fasting approaches.
- NOT currently diagnosed with diabetes.
- NOT taking any appetite suppressants or prescription weight loss medications.
- NOT planning on getting pregnant within the next 6 weeks.
- Do NOT currently have any eating disorders.
- Have NOT lost or gained a significant amount of weight (i.e. 10 pounds or more) within the last 6 months.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Time-restricted feeding (TRF)
Participants will eat the majority of their calories in the day.
More specifically participants will consume 70% of their total calories before 5 pm and the remaining 30% after 5 pm.
|
Participants will receive handouts via email about how to follow each diet
|
|
Comparateur actif: Intermittent fasting (IF)
This involves eating all of one's meals within a specific time (e.g. 8 hours) frame and fasting for the remaining hours (16 hours) in a day.
|
Participants will receive handouts via email about how to follow each diet
|
|
Comparateur actif: Alternate day fasting (ADF)
This involves complete fasting (i.e.
no food or caloric containing beverages, only water consumption) for roughly an entire 36-hour period, followed by an ad libitum feeding day.
|
Participants will receive handouts via email about how to follow each diet
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Weight loss-week 1
Délai: 1 week
|
We will assess weight loss via self-report after 1 week on diet #1
|
1 week
|
|
Weight loss- week 2
Délai: 1 week
|
We will assess weight loss via self-report after 1 week on diet #2
|
1 week
|
|
Weight loss- week 3
Délai: 1 week
|
We will assess weight loss via self-report after 1 week on diet #3
|
1 week
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Energy intake-week 1
Délai: 6 weeks
|
Energy (kcal) intake will be assessed after 1 week on diet #1
|
6 weeks
|
|
Energy intake- week 2
Délai: 6 weeks
|
Energy (kcal) intake will be assessed after 1 week on diet #2
|
6 weeks
|
|
Energy intake- week 3
Délai: 6 weeks
|
Energy (kcal) intake will be assessed after 1 week on diet #3
|
6 weeks
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Gabrielle Turner-McGrievy, University of South Carolina
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- Pro00089911
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .