- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00628030
NOURISH: Nourishing Our Understanding of Role Modeling to Improve Support and Health (NOURISH)
Parent Skills Training to Enhance Weight Loss in Overweight Children
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Pediatric overweight is a national public health concern. The percentage of overweight children in the U.S. between the ages of 6 and 11 has nearly tripled in the last 3 decades. African American children are particularly at risk. Pediatric overweight is associated with numerous physical and psychological health problems. Moreover, overweight children are at significant risk for obesity in adulthood. Thus, a focus on pediatric overweight is an important step in the prevention of adult obesity.
Despite the urgent need for pediatric overweight interventions, outcomes of some of the most rigorous treatments are, at best, mixed. Although research has found that including parents in interventions for pediatric overweight has positive effects on outcomes, parental involvement is usually limited. Moreover, relatively few studies have included sufficient numbers of lower-SES, African American participants, a group at increased risk for pediatric overweight and associated complications. This study will evaluate the efficacy of an intensive intervention targeting ethnically diverse parents of overweight, children ages 6-11 (NOURISH-Nourishing Our Understanding of Role Modeling to Improve Support and Health).
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
Virginia
-
Richmond, Virginia, États-Unis, 23284
- Virginia Commonwealth University
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- To qualify for participation, parents/caregivers must have a child between the ages of 6 and 11 with a BMI > the 85th percentile [128].
- This child must also primarily reside in the participating caregiver's home.
- Participants also need to speak English fluently, and be able to understand and follow basic instructions and perform simple exercises.
Exclusion Criteria:
Caregivers are ineligible if they are:
- non-ambulatory,
- pregnant,
- or have a clinical diagnosis that may be negatively impacted by exercise.
- Parents whose children have a medical condition or developmental disorder that precludes weight loss using conventional diet and exercise methods are also ineligible for participation.
All parents meeting study criteria will be offered participation in the randomized trial comparing NOURISH with a control group.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Expérimental: NOURISH
The first 2 waves and second 2 waves of participants will receive a 12 and 6 week face-to-face intervention (NOURISH), respectively.
The interventions differ only in duration.
They cover the same concepts which are grounded in Social Cognitive Theory (SCT).
Throughout the interventions the influence of social learning on behavioral outcomes (e.g., parent's modeling of healthy behavior) will be emphasized.
Weekly topics provide information about implementing healthy lifestyle behaviors, authoritarian parenting approaches, and strategies for overcoming barriers to change.
Parents will receive pedometers for themselves and 1 of their children.
A one-hour booster session will be available for all intervention participants 2 months after completion of the interventions.
|
Participants in the NOURISH intervention will have 6 weekly face-to-face parent group sessions regarding healthy eating and physical activity.
|
Comparateur placebo: Wellness Group
The placebo control group will attend a group session moderated by an independent interventionist.
This interventionist will be blinded to the Specific Aims and hypotheses of this study.
The session will address the role of diet and exercise in pediatric overweight.
In addition, control parents will receive pedometers (and instructions on their use) for themselves and 1 of their children.
Finally, control participants will be mailed publicly available brochures on pediatric overweight on 2 occasions during the study.
Control participants will also be sent home one additional packet of information (essentially a review of previous mail outs) 2 months after post-testing.
|
Participants in the Wellness Group will have one face-to-face group meeting and information regarding healthy eating and physical activity will be provided on a regular basis via mail.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Child BMI
Délai: Basline, Posttest
|
Children's height and weight were measured and then plotted on the CDC Growth Charts to obtain BMI%ile for age and gender.
|
Basline, Posttest
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Child Feeding
Délai: Basline, Posttest
|
The Child Feeding Questionnaire (CFQ) measured parental approaches to and attitudes about feeding their children and the subscale "concern about child's weight" is reported below in the table.
The subscale score was calculated by averaging the items (subscale score range: 3 to 15, higher scores represent greater risk).
To compare groups, change scores were calculated by subtracting post-test values from baseline values (negative scores indicate decline in parental concern from baseline to post-test).
|
Basline, Posttest
|
Child Quality of Life
Délai: Basline, Posttest
|
Pediatric Health-Related Quality of Life (PedsQL4.0) change scores from baseline to posttest We reported the Total Score. The PedsQL4.0 response scale ranges from 0 - 4. The items are reverse-scored for interpretability and higher scores indicate higher quality of life. We used the Total Score, or the mean computed as the sum of all the items over the number of items answered on all the Scales. The current report did not provide subscores. |
Basline, Posttest
|
Parental BMI
Délai: Baseline, Posttest
|
Height and weight were measured by trained staff and used to calculate BMI.
Change scores of parental BMI from baseline to posttest were calculated to show difference between treatment arms.
|
Baseline, Posttest
|
Parental Dietary Intake of Fat
Délai: Baseline, Posttest
|
Parents completed a 3 day dietary record which was reviewed by a dietitian and analyzed using the Nutrition Data System Software (NDS-R) to calculate parental fat intake.
Change scores were calculated by subtracting post-test values from baseline values; thus, a negative score indicates a greater reduction in fat intake at post-testing.
|
Baseline, Posttest
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Suzanne E. Mazzeo, Ph.D., Virginia Commonwealth University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
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 (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- PT101376
- 1R03HD056050-01A1 (Subvention/contrat des NIH des États-Unis)
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 .
Essais cliniques sur NOURISH
-
University of South FloridaNational Cancer Institute (NCI)RecrutementNOURISH-T+ : Promouvoir des comportements sains en matière d'alimentation et d'exercice (NOURISH-T+)Cancer | Obésité, Enfance | SurvieÉtats-Unis
-
St. Mary's University, TwickenhamGoldsmiths, University of London; London South Bank UniversityComplété
-
Aspire Nutrition, LLPPas encore de recrutementTroubles nutritionnels | Fatigue mentale | Habitudes alimentaires | Régime alimentaire, santé | Troubles de l'alimentation | Comportement alimentaire | Habitudes alimentaires | Stress mental | Pauvre nutrition | Problème de santé mentale | Nutrition, Santé | Manger, Compulsif | Trouble de l'alimentation Fixation...