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Food, Fun, & Fitness Internet Program for Girls: Outcome Evaluation (FFFIPG)

18 januari 2016 uppdaterad av: Deborah Thompson, Baylor College of Medicine

Using Technology to Prevent Obesity Among African American Girls

The purpose of this project is to reduce health disparities in obesity risk among 8-10 year old African American girls using a culturally sensitive and developmentally appropriate internet-based program with no face-to-face interaction. This study will conduct an outcome evaluation to test short and longer term effects on obesity risk.

Studieöversikt

Status

Avslutad

Betingelser

Detaljerad beskrivning

This research will conduct an outcome evaluation on a promising web based obesity prevention program for 8-10 year old African American girls. A pilot study with 80 girls established its feasibility: recruitment goals were met; attrition rates were < 10%; logon rates to the online program were 74.5%; and statistically significant increases in fruit and vegetable consumption and time spent being physically active were observed. The outcome evaluation will recruit 400 child-parent pairs to examine short and longer term effects of the program on obesity risk. It will also conduct mediation analyses to examine pathways of effect. At the end of the study, the web based program will be hosted on the CNRC web site. Although the use of the internet as a method for changing health behavior is not new, the use of an internet program alone, with no face to face interaction, is novel. This is one of the first programs to attempt this, particularly in an at-risk population.

Studietyp

Interventionell

Inskrivning (Faktisk)

342

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Texas
      • Houston, Texas, Förenta staterna, 77030
        • Baylor College of Medicine

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

8 år till 10 år (Barn)

Tar emot friska volontärer

Ja

Kön som är behöriga för studier

Kvinna

Beskrivning

Inclusion Criteria:

  • 8-10 years old
  • healthy
  • African American
  • parent willing to participate in data collection
  • internet access
  • personal email address

Exclusion Criteria:

  • mental, physical, or medical conditions that limit fruit-vegetable consumption, physical activity, or ability to fully participate in the program and/or complete baseline and post assessment data collection
  • taking medications that influence dietary behaviors, appetite, and/or physical activity

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: story plus behaviorial procedures
The girls randomized to this arm of the study will view an interactive story about 6 8-10 year old African American girls who seek to find clues to solve a mystery about the town in which they live. The episodes will contain information about healthy nutrition and physical activity, as well as basic information about physical activity and kitchen safety tips, developmentally appropriate recipes, and portion sizes. Girls randomized to this arm of the study will also engage in key behavior change procedures, such as goal setting, problem solving, and self monitoring.
This is an 8 episode intervention, delivered entirely over the internet. Each episode, girls will view an interactive story in which 6 8-10 year old African American characters attempt to solve a mystery about their town. The online program will include information about healthy nutrition (i.e., consuming more fruit, vegetables, water) and physical activity. There will be two groups; one group (the experimental group) will view the interactive story and participate in key behavior change procedures, such as personal goal setting, problem solving, and self monitoring activities. The second group (the active comparator group) will view the online stories but will not engage in key behavior change procedures.
Aktiv komparator: story only
The girls randomized to this arm of the study will view an interactive story about 6 8-10 year old African American girls who seek to find clues to solve a mystery about the town in which they live. The episodes will contain information about healthy nutrition and physical activity, as well as basic information about physical activity and kitchen safety tips, developmentally appropriate recipes, and portion sizes. Girls randomized to this arm of the study will not engage in key behavior change procedures, such as goal setting, problem solving, and self monitoring.
This is an 8 episode intervention, delivered entirely over the internet. Each episode, girls will view an interactive story in which 6 8-10 year old African American characters attempt to solve a mystery about their town. The online program will include information about healthy nutrition (i.e., consuming more fruit, vegetables, water) and physical activity. There will be two groups; one group (the experimental group) will view the interactive story and participate in key behavior change procedures, such as personal goal setting, problem solving, and self monitoring activities. The second group (the active comparator group) will view the online stories but will not engage in key behavior change procedures.
Inget ingripande: Wait list control
This group will participate in data collection only; after the 3rd data collection point, they will be given access to the intervention

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Body mass index percentile
Tidsram: 6 months
height and weight will be used to calculate BMI percentile
6 months

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
fruit and vegetable consumption
Tidsram: 3 months
dietitian-assisted dietary recalls will be collected using the NDSR system; 2 recalls will be collected (1 week day and 1 weekend day)
3 months
physical activity
Tidsram: 3 months
Accelerometers will be used to assess physical activity at each time point
3 months
self efficacy
Tidsram: 3 months
Standard measures will be used to assess fruit, vegetable, water, and physical activity self efficacy
3 months
home availability
Tidsram: 3 months
standard measures will be used to assess fruit, vegetable, and physical activity equipment home availability
3 months
asking behaviors
Tidsram: 3 months
standard measures will be used to assess child fruit, vegetable, water, and physical activity asking behaviors
3 months
fruit and vegetable consumption
Tidsram: 6 months
dietitian-assisted dietary recalls will be collected using the NDSR system; 2 recalls will be collected at each time point (1 week day and 1 weekend day)
6 months
physical activity
Tidsram: 6 months
Accelerometers will be used to assess physical activity
6 months
self efficacy
Tidsram: 6 months
standard measures will be used to assess fruit, vegetable, water, and physical activity self efficacy
6 months
home availability
Tidsram: 6 months
standard measures will be used to assess fruit, vegetable, and physical activity equipment home availability
6 months
asking behaviors
Tidsram: 6 months
standard measures will be used to assess child fruit, vegetable, water, and physical activity asking behaviors
6 months

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Deborah I Thompson, PhD, Baylor College of Medicine

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

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 januari 2012

Primärt slutförande (Faktisk)

1 maj 2015

Avslutad studie (Faktisk)

1 maj 2015

Studieregistreringsdatum

Först inskickad

21 november 2011

Först inskickad som uppfyllde QC-kriterierna

28 november 2011

Första postat (Uppskatta)

30 november 2011

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

20 januari 2016

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

18 januari 2016

Senast verifierad

1 januari 2016

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • H-27505
  • R01MD005814 (U.S.S. NIH-anslag/kontrakt)

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