- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03012126
Clinical & Community Approaches to Weight Management (CORD 2)
3. februar 2021 oppdatert av: Elsie Taveras, MD, Massachusetts General Hospital
Childhood Obesity Research Demonstration Project 2.0 (CORD 2.0)
This project seeks to build on innovative strategies to optimize the care of low-income children with a BMI ≥ 85th percentile.
To accomplish this goal, investigators will implement a new clinical-community intervention, theoretically grounded in the Integrated Clinical and Community Systems of Care Model, to address obesity through optimized screening and management known to be effective, e-Referrals, Healthy Weight Clinics, and the YMCA's Healthy Weight and Your Child weight management program (originally known as MEND).
The study will examine outcomes for children that matter most to a broad group of stakeholders including parents, clinicians, and public health practitioners as well as inform the care of >7 million children with obesity covered by the Children's Health Insurance Program or Medicaid.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
This is a 2-arm RCT.
Enrolled patients are randomized to a pediatric weight management intervention (PWMI): 1)a Healthy Weight Clinic based at a federally-qualified health center (FQHC), or 2) a modified Healthy Weight and Your Child intervention delivered in YMCAs.
A comparison sample of children receiving care in eight demographically similar FQHCs serve as a comparison group.
Studietype
Intervensjonell
Registrering (Faktiske)
407
Fase
- Ikke aktuelt
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
6 år til 12 år (Barn)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- child is age 6.0 through 12.9 years at referral
- child's BMI meets or exceeds the 85th percentile for age and sex
- parent can read and respond to interviews and questionnaires in English and Spanish
Exclusion Criteria:
- children who do not have at least one parent who is able to follow study procedures for 1 year
- families who plan to leave their primary care health center within the study time frame
- families for whom the primary care clinician thinks the intervention is inappropriate, e.g., emotional or cognitive difficulties
- children who were taking medications that substantially interfere with growth
- children who have a sibling enrolled in the study.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Clinically Based: Healthy Weight Clinic
All families referred to the Healthy Weight Clinic intervention arm will be scheduled for a 30-45 minute orientation clinic visit to orient the child and family to the program.
During this visit, the family will meet with the community health worker who will provide a schedule of clinic visits and dietitian contacts.
The community health worker will assess the child's social and environmental context to allow treatment tailoring.
For the first 6 months, each family will be asked to attend two clinic visits per month and complete weekly 20-30 minute contacts with the dietitian via telephone.
The program aims to deliver approximately 30 contact hours in the 6-month period.
This will be followed by monthly visits to the Healthy Weight Clinic and monthly calls with their dietitian.
|
|
|
Eksperimentell: Community Based: Healthy Weight & Your Child
All families referred to the Healthy Weight and Your Child intervention arm will be scheduled for a 60-minute family information session to orient the child and family to the program.
During this visit, the family will receive information about the program and logistics such as program schedule and format and attendance.
The program is delivered over 12 months, which includes 16 weekly sessions, followed by 4 sessions delivered every other week and concluding with 5 monthly sessions.
Most sessions are 2 hours in length and include a group of about 8-15 children and their caregivers.
The first hour is delivered in a classroom setting and the second hour in an additional area conducive for physical activity.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in Child BMI at 12 months
Tidsramme: 0-12 months
|
0-12 months
|
|
Change in Child BMI percent of the 95th percentile at 12 months
Tidsramme: 0-12 months
|
0-12 months
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Screen Time at 12 months
Tidsramme: 0-12 months
|
Average hours per day of screen time as reported by parent
|
0-12 months
|
|
Change in Sleep Duration at 12 months
Tidsramme: 0-12 months
|
Average hours per day of sleep as reported by parent
|
0-12 months
|
|
Change in Physical Activity at 12 months
Tidsramme: 0-12 months
|
Average number of days (0-7) child is physically active for at least 60 minutes as reported by parent
|
0-12 months
|
|
Change in Diet at 12 months
Tidsramme: 0-12 months
|
Average daily intake of sugar-sweetened beverages and weekly intake of fast food as reported by parent
|
0-12 months
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Elsie Taveras, MD, MPH, MassGeneral Hospital for Children
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Generelle publikasjoner
- Fiechtner L, Perkins M, Biggs V, Langhans N, Sharifi M, O'Connor G, Price S, Locascio J, Kuhlthau K, Kwass JA, Nelson C, Land T, Longjohn M, Lawson V, Hohman K, Taveras EM. Rationale and design of the Clinic and Community Approaches to Healthy Weight Randomized Trial. Contemp Clin Trials. 2018 Apr;67:16-22. doi: 10.1016/j.cct.2018.01.002. Epub 2018 Jan 10.
- Fay C, Castro I, Sierra Velez D, Ruggiero CF, O'Connor G, Perkins M, Luo M, Sharifi M, Neri Mini F, Taveras EM, Kuhlthau K, Fiechtner L. Keys to Achieving Clinically Important Weight Loss: Perceptions of Responders and Nonresponders in the Clinic and Community Approaches to Healthy Weight Trial. Child Obes. 2022 Oct 28. doi: 10.1089/chi.2022.0112. Online ahead of print.
- Harshman SG, Castro I, Perkins M, Luo M, Barrett Mueller K, Cena H, Portale S, Raspini B, Taveras E, Fiechtner L. Pediatric weight management interventions improve prevalence of overeating behaviors. Int J Obes (Lond). 2022 Mar;46(3):630-636. doi: 10.1038/s41366-021-00989-x. Epub 2021 Dec 3.
- Sierra Velez D, Simione M, Castro I, Perkins M, Luo M, Taveras EM, Fiechtner L. Effects of a Pediatric Weight Management Intervention on Parental Stress. Child Obes. 2022 Apr;18(3):160-167. doi: 10.1089/chi.2021.0146. Epub 2021 Oct 7.
- Fiechtner L, Perkins M, Biggs V, Langhans N, Sharifi M, Price S, Luo M, Locascio JJ, Hohman KH, Hodge H, Gortmaker S, Torres S, Taveras EM. Comparative Effectiveness of Clinical and Community-Based Approaches to Healthy Weight. Pediatrics. 2021 Oct;148(4):e2021050405. doi: 10.1542/peds.2021-050405. Epub 2021 Sep 1.
- Atkins M, Castro I, Sharifi M, Perkins M, O'Connor G, Sandel M, Taveras EM, Fiechtner L. Unmet Social Needs and Adherence to Pediatric Weight Management Interventions: Massachusetts, 2017-2019. Am J Public Health. 2020 Jul;110(S2):S251-S257. doi: 10.2105/AJPH.2020.305772.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
1. desember 2016
Primær fullføring (Faktiske)
1. september 2019
Studiet fullført (Faktiske)
1. september 2019
Datoer for studieregistrering
Først innsendt
12. desember 2016
Først innsendt som oppfylte QC-kriteriene
5. januar 2017
Først lagt ut (Anslag)
6. januar 2017
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
8. februar 2021
Siste oppdatering sendt inn som oppfylte QC-kriteriene
3. februar 2021
Sist bekreftet
1. februar 2021
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 937121
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Ja
IPD-planbeskrivelse
Individual-level data may be shared upon request, under the conditions that an analysis plan is prepared and approved by the PI/Co-Is, IRB approval has been obtained, and all necessary data sharing agreements have been executed.
IPD-delingstidsramme
Data can be requested by emailing the PI or Project Manager.
Tilgangskriterier for IPD-deling
- An analysis plan is prepared and approved by the PI/Co-Is
- IRB approval has been obtained, and
- all necessary data sharing agreements have been executed.
IPD-deling Støtteinformasjonstype
- Studieprotokoll
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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