- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01357551
Maintenance After Initiation of Nutrition TrAINing (MAINTAIN)
13 septembre 2016 mis à jour par: VA Office of Research and Development
Maintenance After Initiation of Nutrition TrAINing (MAINTAIN)
Obesity is the second leading cause of preventable deaths in the United States and is associated with a wide range of diseases.
In people who are obese, weight loss improves blood pressure, dyslipidemia, glycemia, and arthritis symptoms; reduces medication use for several disease processes; increases physical functioning; and enhances health-related quality of life.
The current study evaluated a theoretically informed maintenance intervention.
If effective, this intervention could reduce the need for future clinic visits to treat obesity and its many associated illnesses.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
Obesity is the second leading cause of preventable deaths in the United States and is associated with a wide range of diseases.
In people who are obese, weight loss improves blood pressure, dyslipidemia, glycemia, and arthritis symptoms; reduces medication use for several disease processes; increases physical functioning; and enhances health-related quality of life.
Despite these benefits, most patients who achieve weight loss regain much of this weight within a year, and few effective behavioral weight maintenance interventions have been identified.
Thus, there is a dire need for effective interventions that can promote weight loss maintenance.
Theoretical and empirical studies indicate that behavior maintenance is a distinct state that involves different psychological processes and behavioral skills than initial behavior change.
The few trials that have tested weight loss maintenance interventions have not taken this distinction into account, which may partially explain their modest findings.
The current study evaluated the efficacy of a theoretically informed maintenance intervention compared to usual care.
If efficacious, this intervention could reduce the need for future clinic visits to treat obesity and its many associated illnesses and could serve as a model for redesigning the MOVE! program.
This 3.5-year study involved a two-arm, randomized, controlled trial.
During the run-in phase, Veterans with BMI 30 kg/m2 participated in a 4-month, intensive, group-based weight loss program.
Participants who lost at least 4 kg by the end of 4 months (n=222) were randomized to receive (a) usual care (n=112) for 56 weeks or (b) a theoretically-informed maintenance intervention (n=110) for 42 weeks months, followed by 14 weeks of no intervention contact to examine sustainability.
The maintenance intervention involved in-person group visits that transition to individualized telephone calls, and the frequency of contact with the interventionist gradually tapered over time.
Outcomes were assessed at randomization and at weeks 14, 26, 42, and 56 post-randomization.
The hypotheses are that the maintenance intervention will result in at least 3.5 kg greater weight loss and greater improvements in caloric intake and physical activity over the study period, and that it will be cost-effective, compared to usual care.
Type d'étude
Interventionnel
Inscription (Réel)
222
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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North Carolina
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Durham, North Carolina, États-Unis, 27705
- Durham VA Medical Center, Durham, NC
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans à 74 ans (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- BMI >= 30 kg/m2
- Desire to lose weight
- Agrees to attend regular visits per study protocol
- Has a provider at the Durham Veterans Affairs Medical Center
Exclusion Criteria:
- Age >= 75 years old,
- Most recent serum creatinine >2.0 mg/dL in men, >1.7 mg/dL in women),
- Liver disease (cirrhosis, jaundice, or other stigmata of advanced liver disease),
- Type 1 diabetes,
- Hemoglobin A1c >= 12% in past 6 months
- unstable angina or coronary ischemia workup in past 3 months
- Female: pregnancy, breastfeeding, or lack of birth control if premenopausal
- Transplant recipient
- Pacemaker or defibrillator (bioelectric impedance assessment might interfere with these)
- Average systolic blood pressure in the past year >= 160 mmHg AND most recent BP >=160 mmHg
- Dementia, severe psychiatric illness (e.g., major depression), alcohol problem, or illicit substance abuse
- Weight loss of at least 10 lb in previous 3 months
- Enrollment in a weight loss program
- Unable to stand for study measurements
- history of weight loss surgery
- cancer not in remission
- current use of appetite suppressants or weight loss medication
- lack of reliable transportation or telephone
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Maintenance intervention
Participants receive a theoretically-informed maintenance intervention for 42 weeks, followed by 14 weeks of no intervention contact to examine sustainability.
The maintenance intervention involves in-person group visits that transition to individualized telephone calls, and the frequency of contact gradually decreases over time.
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Theoretically-informed maintenance intervention that involves in-person group visits that transition to individualized telephone calls, and the frequency of contact gradually decreases over time.
|
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Aucune intervention: Usual care
Participants receive usual care for 56 weeks
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Weight
Délai: 56 weeks post-randomization
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56 weeks post-randomization
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Estimated Daily Caloric Intake
Délai: 56 weeks
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Based on self-report using Block Brief Food Frequency Questionnaire
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56 weeks
|
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Estimated Metabolic Minutes of Walking Per Week
Délai: 56 weeks
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self-reported based on short form of International Physical Activity Questionnaire
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56 weeks
|
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Estimated Metabolic Minutes of Moderate Physical Activity Per Week
Délai: 56 weeks
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self-reported based on short form of International Physical Activity Questionnaire
|
56 weeks
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Corrine I Voils, PhD, Durham VA Medical Center, Durham, NC
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Publications générales
- Voils CI, Gierisch JM, Yancy WS Jr, Sandelowski M, Smith R, Bolton J, Strauss JL. Differentiating Behavior Initiation and Maintenance: Theoretical Framework and Proof of Concept. Health Educ Behav. 2014 Jun;41(3):325-36. doi: 10.1177/1090198113515242. Epub 2013 Dec 16.
- Voils CI, Gierisch JM, Olsen MK, Maciejewski ML, Grubber J, McVay MA, Strauss JL, Bolton J, Gaillard L, Strawbridge E, Yancy WS Jr. Study design and protocol for a theory-based behavioral intervention focusing on maintenance of weight loss: the Maintenance After Initiation of Nutrition TrAINing (MAINTAIN) study. Contemp Clin Trials. 2014 Sep;39(1):95-105. doi: 10.1016/j.cct.2014.08.002. Epub 2014 Aug 10.
- Funk LM, Grubber JM, McVay MA, Olsen MK, Yancy WS, Voils CI. Patient predictors of weight loss following a behavioral weight management intervention among US Veterans with severe obesity. Eat Weight Disord. 2018 Oct;23(5):587-595. doi: 10.1007/s40519-017-0425-6. Epub 2017 Aug 29.
- Voils CI, Olsen MK, Gierisch JM, McVay MA, Grubber JM, Gaillard L, Bolton J, Maciejewski ML, Strawbridge E, Yancy WS Jr. Maintenance of Weight Loss After Initiation of Nutrition Training: A Randomized Trial. Ann Intern Med. 2017 Apr 4;166(7):463-471. doi: 10.7326/M16-2160. Epub 2017 Feb 21.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude
1 août 2012
Achèvement primaire (Réel)
1 novembre 2015
Achèvement de l'étude (Réel)
1 novembre 2015
Dates d'inscription aux études
Première soumission
13 mai 2011
Première soumission répondant aux critères de contrôle qualité
18 mai 2011
Première publication (Estimation)
20 mai 2011
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
2 novembre 2016
Dernière mise à jour soumise répondant aux critères de contrôle qualité
13 septembre 2016
Dernière vérification
1 septembre 2016
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- IIR 11-040
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 .