Family Dietary Coaching to Improve Nutritional Intakes and Body Weight Control

NCT00456911 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2020

Last updated 2008-02-13

No results posted yet for this study

Summary

We hypothesize that Family Dietary Coaching for one school year will allow a nutritional shift towards following recommendations and improve health indicators in free-living children and adults.

Conditions

  • Primary Prevention
  • Obesity Prevention
  • Body Weight Control

Interventions

BEHAVIORAL

Fat and carbohydrate controlled diet

Sponsors & Collaborators

  • Ministry of Higher Education and Research, France

    collaborator OTHER_GOV
  • Paris Academy (Rectorat de Paris)

    collaborator UNKNOWN
  • Avenance Enseignement

    collaborator UNKNOWN
  • Fondation Louis Bonduelle

    collaborator UNKNOWN
  • Centre d'Etudes et de Documentation du Sucre

    lead OTHER

Principal Investigators

  • Alain BOULIER, MD, PHD · Department of Nutrition and Functional Investigations, INSERM U695, Bichat-Claude Bernard Hospital, Paris, France

  • Dominique-Adèle CASSUTO, MD · Paris, France

  • Judith CHWALOW, PHD · Department of Nutrition, EA3502, Hôtel-Dieu, Paris, France

  • Pierre COMBRIS, PHD · INRA-CORELA, Ivry-sur-Seine, France

  • Charles COUET, MD · INSERM E211, Tours Hospital, Tours, France

  • Béatrice JOURET, MD · Department of Pediatrics, Children's Hospital, Toulouse, France

  • Monique ROMON, MD · Department of Nutrition, EA2694 Lille2 University, Lille, France

  • Chantal SIMON, MD, PhD · Louis Pasteur University, Medical Faculty, EA 1801, Strasbourg, France

  • Maïté TAUBER, MD · Department of Pediatrics, Children's Hospital, Toulouse, France

  • Paul VALENSI, MD · Department of Endocrinology, CRNH Ile-de-France, Jean Verdier Hospital, Bondy, France

  • Francis BORNET, MD, PHD · Nutri-Health, Rueil-Malmaison, France

  • Damien PAINEAU, MS · Nutri-Health, Rueil-Malmaison, France

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-03-31
Completion
2006-07-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00456911 on ClinicalTrials.gov