A Trial To Study The Effects Of Group Versus Individual Dietary Counseling In Pediatric Obesity
A Randomized Controlled Trial To Study The Effects Of Group Versus Individual Dietary Counseling In Pediatric Obesity
Aim 1 - The primary aim of the study is to assess whether group counseling is a non-inferior intervention compared to the usual care of individual counseling in the management of childhood obesity. In order to achieve this aim, the investigators will compare the mean change in BMI after 6 months of intervention in the two study arms.
Aim 2 - The secondary aim of the study is to determine if the change in BMI is associated with changes in the dietary composition, physical activity and metabolic profile.
Studie Overzicht
Gedetailleerde beschrijving
This is a non-inferiority study to determine the sample size needed for a larger study to explore an intervention strategy focused on nutrition counseling to maximize weight loss and minimize cardiovascular risk factors in obese children and adolescents. This is a prospective parallel arm, randomized trial, to study the impact of nutritional counseling in an individual vs. group setting. There will be a total of four groups. Obese pre-adolescents (ages 9-12) and adolescents (ages 13-17) will be randomized into two interventions: individual nutrition counseling or group nutrition counseling. Subjects will receive the same information in both interventions. All content will be developed prior to starting the intervention. Each group session will have a maximum of 7 children with 1 parent/caregiver per child and a minimum of 5 children with a caregiver. Group sessions will be one time a month for 60 minutes (30 minutes for dietetic session and 30 minutes for discussion/questions) and individual sessions will be one time a month for 30 minutes. There will be 6 sessions for each group.
All groups will receive standard of care for physical fitness counseling which includes recommending 1 hour of physical activity a day and limiting screen time to less than 2 hours a day. All groups will be evaluated for depression and appropriately referred if found to be depressed. Behavioral strategies, like mindful eating, will be included in the nutrition education.
Studietype
Inschrijving (Werkelijk)
Fase
- Niet toepasbaar
Contacten en locaties
Studie Locaties
-
-
New York
-
Bronx, New York, Verenigde Staten, 10467
- Albert Einstein College of Medicine West Campus CRC
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Subjects 9-17 years of age with a BMI percentile for age of ≥95
- Subjects must be able to attend monthly sessions with a parent and/or guardian.
Exclusion Criteria:
- Subjects with diabetes at baseline, mental or psychological disease that would interfere with understanding, disease or medication causing obesity or weight loss, and participants in an alternative weight management program will not be included in the study.
- Subjects with impaired glucose tolerance will not be excluded from participation.
- Non-English speaking subjects will not be excluded.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Actieve vergelijker: Group nutritional counseling
In this arm, the Nutritionist will conduct the nutritional counseling with numerous patient families as a group
|
Participants enrolled will be randomized into group nutrition counseling or individual nutrition counseling classes, for a total of 6 classes.
Classes will meet one time a month.
Classes will cover topics including nutrition, exercise, and behavior to promote healthy eating.
|
|
Actieve vergelijker: Individual nutritional counseling
In this arm the nutritionist conducts the nutritional counseling with one patient family at a time
|
Participants enrolled will be randomized into group nutrition counseling or individual nutrition counseling classes, for a total of 6 classes.
Classes will meet one time a month.
Classes will cover topics including nutrition, exercise, and behavior to promote healthy eating.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change I Mean Body Mass Index
Tijdsspanne: Baseline, month 6
|
The primary aim of the study is to assess whether group counseling is a non-inferior intervention compared to the usual care of individual counseling in the management of childhood obesity.
In order to achieve this aim, investigators will compare the mean change in BMI after 6 months of intervention in the two study arms.
As per previous studies, it is expected the group intervention arm to achieve a mean BMI reduction of 0.8 +/- 1.4 greater than the control arm.
The study also posits that a difference in mean BMI change as low as 0.1 would be clinically equivalent.
|
Baseline, month 6
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change in BMI with diet
Tijdsspanne: Baseline, month 6
|
The secondary aim of the study is to determine if the change in BMI is associated with changes in the dietary composition.
All the secondary outcomes will be measured by Pearson correlation coefficients or multi-variable linear regression models as appropriate to calculate this.
|
Baseline, month 6
|
|
Change in BMI with physical activity
Tijdsspanne: Baseline, month 6
|
The study will assess if there is a change in BMI with increased physical activity
|
Baseline, month 6
|
|
Change in BMI with metabolic profile
Tijdsspanne: Baseline, month 6
|
Study will assess if the change in BMI affects Metabolic profile of the subject.
|
Baseline, month 6
|
Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Lisa Underland, MD, Albert Einstein College of Medicine
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing (Werkelijk)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 2012-214
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .
Klinische onderzoeken op Nutritional Counseling
-
Cedars-Sinai Medical CenterUniversity of Michigan; NestléVoltooid
-
Yale UniversityNational Institute of Mental Health (NIMH)VoltooidObesitas | Schizofrenie | Schizo-affectieve stoornisVerenigde Staten
-
CNAO National Center of Oncological HadrontherapyWervingHoofd-halskankerItalië
-
Hanyang UniversityVoltooid
-
Cardiocentro TicinoVoltooidPostoperatief deliriumZwitserland
-
Maastricht University Medical CenterDSM Nutritional Products, Inc.; The Netherlands Asthma FoundationVoltooidLongziekte, chronisch obstructiefNederland
-
Maastricht University Medical CenterDSM Nutritional Products, Inc.Onbekend
-
Hungarian Institute of CardiologySemmelweis UniversityOnbekendKwaliteit van het leven | Aortaklepstenose | HartklepaandoeningHongarije