- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00877994
Nurture: A Program for Mothers With Histories of Disordered Eating
17. maj 2016 opdateret af: University of North Carolina, Chapel Hill
Breaking the Cycle of Risk: Intervention for Mothers With Eating Disorders
Nurture is a collaborative pilot study for mothers of children under the age of 3 who have suffered from disordered eating in the past.
It is coordinated by the University of North Carolina at Chapel Hill, Duke University and Virginia Commonwealth University and sponsored by the National Institute of Mental Health.
Nurture hopes to promote confident parenting and a positive meal times.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Mothers who have struggled with disordered eating or body image struggles are often concerned how best to provide proper nutrition to their child and/or model healthy eating behavior.
We have developed a curriculum that provides information about how to establish healthy eating patterns and social support for mothers with children under three years of age.
The curriculum will be delivered in a support group format led by co-therapists affiliated with the UNC Eating Disorder Program.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
28
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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North Carolina
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Chapel Hill, North Carolina, Forenede Stater, 27516
- University of North Carolina Chapel Hill
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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
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- Has met lifetime DSM-IV criteria for anorexia nervosa (AN), bulimia nervosa (BN), or eating disorder not otherwise specified (EDNOS: including subthreshold AN, BN, and purging disorder, but excluding BED)
- BMI > 18.5 maintained for at least three months
- Has not met threshold criteria for AN or BN in the previous 28 days according to the Eating Disorders Examination, although subthreshold status or active residual symptomatology will not preclude entry
- Age 18 or older
- Has a child between the ages of 1 month and 2 years, 12 months old
Exclusion Criteria:
- Alcohol or drug dependence in the past year
- Current significant suicidal ideation reported during the assessment or on the BDI-II at baseline
- Developmental disability that would impair the ability of the participant to benefit from the intervention
- Psychosis, including schizophrenia, or bipolar I disorder
- Any families who have been the subject of social service inquiries
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: Immediate
This group will receive the nurture group therapy immediately after enrolling in the study.
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Participants will be randomly assigned (like the flip of a coin) to either receive the curriculum immediately (immediate group) or at a later time point approximately 16 weeks later (delayed group).
Both groups will receive 16, 90 minute long group sessions delivered over 4 months.
Groups will include 4-8 mothers and one or two co-therapists.
Andre navne:
Participants will be randomly assigned (like the flip of a coin) to either receive the curriculum immediately (immediate group) or at a later time point approximately 16 weeks later (delayed group).
Both groups will receive 16, 90 minute long group sessions delivered over 4 months.
Groups will include 4-8 mothers and one or two co-therapists.
The curriculum will focus on increasing positive healthy eating patterns in children of mothers who have had disordered eating and body image struggles.
Andre navne:
|
Aktiv komparator: Delayed
This group will receive the nurture group therapy 16 weeks after enrolling in the study.
|
Participants will be randomly assigned (like the flip of a coin) to either receive the curriculum immediately (immediate group) or at a later time point approximately 16 weeks later (delayed group).
Both groups will receive 16, 90 minute long group sessions delivered over 4 months.
Groups will include 4-8 mothers and one or two co-therapists.
Andre navne:
Participants will be randomly assigned (like the flip of a coin) to either receive the curriculum immediately (immediate group) or at a later time point approximately 16 weeks later (delayed group).
Both groups will receive 16, 90 minute long group sessions delivered over 4 months.
Groups will include 4-8 mothers and one or two co-therapists.
The curriculum will focus on increasing positive healthy eating patterns in children of mothers who have had disordered eating and body image struggles.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
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Parenting self-efficacy
Tidsramme: 7 months
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7 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Nancy Zucker, PhD, Duke University
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. april 2008
Primær færdiggørelse (Faktiske)
1. juni 2012
Studieafslutning (Faktiske)
1. juni 2012
Datoer for studieregistrering
Først indsendt
6. april 2009
Først indsendt, der opfyldte QC-kriterier
7. april 2009
Først opslået (Skøn)
8. april 2009
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
19. maj 2016
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
17. maj 2016
Sidst verificeret
1. maj 2016
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 08-0236
- R34MH080750 (U.S. NIH-bevilling/kontrakt)
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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