- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00877994
Nurture: A Program for Mothers With Histories of Disordered Eating
17 maj 2016 uppdaterad av: 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.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Interventionell
Inskrivning (Faktisk)
28
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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North Carolina
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Chapel Hill, North Carolina, Förenta staterna, 27516
- University of North Carolina Chapel Hill
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Kvinna
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / 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.
Andra namn:
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.
Andra namn:
|
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.
Andra namn:
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.
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
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Parenting self-efficacy
Tidsram: 7 months
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7 months
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Samarbetspartners
Utredare
- Huvudutredare: Nancy Zucker, PhD, Duke University
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 april 2008
Primärt slutförande (Faktisk)
1 juni 2012
Avslutad studie (Faktisk)
1 juni 2012
Studieregistreringsdatum
Först inskickad
6 april 2009
Först inskickad som uppfyllde QC-kriterierna
7 april 2009
Första postat (Uppskatta)
8 april 2009
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
19 maj 2016
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
17 maj 2016
Senast verifierad
1 maj 2016
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 08-0236
- R34MH080750 (U.S.S. NIH-anslag/kontrakt)
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
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