- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00438555
Randomized, Controlled, Open, Comparative Intervention Study for Obesity Prevention in Children (4055obesityprv)
18. marts 2015 opdateret af: Rabin Medical Center
Randomized, controlled, open, comparative intervention study in 270 children at risk for obesity.Patients will be randomly allocated into one of two behavior intervention groups or control group in ratio of 1:1:1.The study will consist of two main periods: an intervention period of 3 months followed by 21 months of a follow up period.
During the intervention period, participants (parents or both parents and children, depending on randomization) will attend a behavior intervention program once a week, each session will last one hour and would be guided by dietician and psychologist.
Follow up visits will be performed at the clinic (for participants in al 3 groups) at months 0, 3, 12 and 24.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Randomized, controlled, open, comparative intervention study in 270 children at risk for obesity.
Objectives:
- To develop an intervention program for obesity prevention in children aged 5-10 years old, who are at risk to develop obesity
- To compare between the efficacy of two different intervention programs and a control group in preventing obesity in the short and the long term.
- To evaluate the role and significance of including parents in an intervention program for obesity prevention.
- To identify demographic parameters, lifestyle characteristic and biochemical markers that predict the risk of developing obesity and the response for treatment.
Randomization:
Patients will be randomly allocated into one of two intervention groups or control group in ratio of 1:1:1. Each group will contain 12-15 participants.
Intervention groups:
- parent's group- only parents will take part at the intervention program.
- Parents and children group- both children and parents will take part at the intervention program, in two separate sessions.
Methods:
- The study will be consist of two main periods: an intervention period of 3 months followed by 21 months of a follow up period. During the intervention period, participants (parents or both parents and children, depending on randomization) will attend a behavior intervention program once a week, each session will last one hour and would be guided by dietician and psychologist. Follow up visits will be performed at the clinic (for participants in all 3 groups) at months 0, 3, 12 and 24.
- Height, weight, fat mass and waist circumference will be measured at 0, 3, 12 and 24 month. Height and weight of parents will also be measured at these visits.
- Physical examination will be performed at 0, 3, 12 and 24 month.
- Psychological and nutritional questionnaire (depression, quality of life and self estimation) will be filled at 0, 3, 12 and 24 month.
- Fasting blood tests for: chemistry, hematology, lipids, glucose, insulin, TSH, adiponectin, IL-6 and TNFα will be performed at 0, 3, 12 and 24 month.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
248
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
Petach Tikva, Israel, 49202
- Schneider Children Medical Center of Israel
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
5 år til 10 år (Barn)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Children aged 5-10 years old
- BMI in 85-98 percentile
- Both parents signing informed consent form
Exclusion Criteria:
- Chronic disease or chronic use of medication
- Incapability to perform all study procedure
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Parent's group
3 months workshop of parents intervention, guided by dietician and phycologist
|
3 months workshop of parents intervention, guided by dietician and phycologist
|
|
Eksperimentel: Parents and children group
3 months workshops of parents and children intervention, guided by dietician and phycologist
|
3 months workshops of parents and children intervention, guided by dietician and phycologist
|
|
Ingen indgriben: Control group
control group, no intervention, medical follow up only
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
BMI
Tidsramme: 24 month
|
24 month
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Moshe Phillip, Prof, MD, Schneider Children Medical Center
- Ledende efterforsker: Joseph Meyerovitch, Dr, MD, Schneider Children Medical Center
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. oktober 2006
Primær færdiggørelse (Faktiske)
1. oktober 2014
Studieafslutning (Faktiske)
1. december 2014
Datoer for studieregistrering
Først indsendt
21. februar 2007
Først indsendt, der opfyldte QC-kriterier
21. februar 2007
Først opslået (Skøn)
22. februar 2007
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
19. marts 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
18. marts 2015
Sidst verificeret
1. juli 2014
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- rmc004055ctil
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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