- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00949637
Scouting Nutrition and Activity Program (SNAP)
March 7, 2017 updated by: Richard R. Rosenkranz, Kansas State University
A Site-Randomized Controlled Trial for Health Promotion in Girl Scouts: Healthier Troops in a SNAP
The purpose of the study was to evaluate the effectiveness of an intervention designed to prevent obesity by improving the environmental characteristics of Girl Scouts troop meetings.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Girls and parents affiliated with Girl Scouts Juniors programs completed a questionnaire prior to the beginning of an intervention program, and again after the program.
Children responded to previously validated questionnaire items assessing demographics, parent-child connectedness, parent-child physical activity, screen time usage, family meal-time environment, consumption of fruits and vegetables, soda, and fast food.
Parents completed a similar questionnaire, assessing demographics, parent-child connectedness, parent-child physical activity, family mealtime environment, parenting style and parenting practices.
Children were also assessed on height and weight to characterize their risk for overweight status.
Questionnaires and environmental observations were used to assess the effectiveness of an intervention designed to improve the family meal-time environment at home, as well as helping to assess the relationships between parental factors and family health-related behavior.
Study Type
Interventional
Enrollment (Actual)
76
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Kansas
-
Manhattan, Kansas, United States, 66506
- Kansas State University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
8 years to 12 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Girls had to be attending members of Girl Scouts in one of our included troops.
- The troop needed to be a registered Girl Scouts Juniors troop, consisting of girls primarily in the 4th and 5th grades.
- To be officially registered, the troop leaders were required to complete Girl Scout leader training and pass a criminal background check.
- To be included, the troops also needed to meet at least twice per month, have meeting facilities capable of allowing physical activity and food preparation.
- Also, troops needed to have initial agreement of leaders and parents for the troop to participate in a research study.
Exclusion Criteria:
- An inability to speak or read English.
- Troops not primarily composed of Girl Scouts Juniors, not regularly meeting during the study period, or not having leader and parental consensus approval for troop participation.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Scouting curricular implementation
Intervention group will receive a curriculum based on social cognitive theory, wherein children will be taught skills in a supportive environment to improve their self efficacy and proxy efficacy toward eating healthful meals and being physically active with a parent.
Troop leaders and parents will provide support, and help girls to create healthy opportunities in the home environment.
Simultaneously, girls will be taught skills to improve the family mealtime environment, to bolster asking skills toward healthy behavior, to self-monitor healthy behavior, and to set goals for healthy behavior.
|
Intervention group will receive a curriculum based on social cognitive theory, wherein children will be taught skills in a supportive environment to improve their self efficacy and proxy efficacy toward eating healthful meals and being physically active with a parent.
Troop leaders and parents will provide support, and help girls to create healthy opportunities in the home environment.
Simultaneously, girls will be taught skills to improve the family mealtime environment, to bolster asking skills toward healthy behavior, to self-monitor healthy behavior, and to set goals for healthy behavior.
Other Names:
|
|
Active Comparator: Standard-care attentional control
Control troops complete usual troop meeting activities.
Control troops receive equal observation time, equal pretest and posttest assessment, and equal study scrutiny.
|
Control troops complete usual troop meeting activities.
Control troops receive equal observation time, equal pretest and posttest assessment, and equal study scrutiny.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Body mass index percentile ranking
Time Frame: 5 months
|
5 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Obesity-related behaviors
Time Frame: 5 months
|
5 months
|
|
Troop environmental encouragement and opportunities for healthful eating and physical activity
Time Frame: continuous
|
continuous
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Richard R. Rosenkranz, PhD, Kansas State University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2007
Primary Completion (Actual)
May 1, 2008
Study Completion (Actual)
May 1, 2008
Study Registration Dates
First Submitted
July 21, 2009
First Submitted That Met QC Criteria
July 29, 2009
First Posted (Estimate)
July 30, 2009
Study Record Updates
Last Update Posted (Actual)
March 9, 2017
Last Update Submitted That Met QC Criteria
March 7, 2017
Last Verified
March 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SF SNAP y1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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