Evaluation of a Commercial Gaming Impact in a Childhood Obesity Intervention
|ClinicalTrials.gov Identifier: NCT01757925|
Recruitment Status : Completed
First Posted : December 31, 2012
Last Update Posted : December 31, 2012
Recently, researchers have been interested in the use of game play, mechanics and psychology for health-related engagement and behavior change. While initial studies have shown some increases in health knowledge and/or behavior through gaming, there remains concern that the vehicle for change is associated with a perceived sedentary behavior (6).
More recently, commercially available gaming devices are able to directly promote physical activity through a new set of "kinetic controllers" added to the gaming experience. UHG plans to evaluate the most recent of these kinetic controller technologies in the context of a second iteration of JOIN (described above) to be implemented among a pilot group of overweight and/or obese children whose BMI percentile is above the 85th.
This study will evaluate the effect of a commercial controller-free Exercise Gaming and Entertainment Experience (EGEE) on physical activity levels in the context of a weight management program in approximately 70 children ages 6 to12. The study will compare the differences in physical activity levels over 16 weeks in two groups of children.
|Condition or disease||Intervention/treatment||Phase|
|Childhood Obesity||Behavioral: weight managment program Other: Active Gaming||Phase 4|
The Center for Health Reform and Modernization at UHG will compare levels of physical activity, assessed by accelerometry, among children randomly assigned to WMA or WM+E groups. Specific aims of this evaluation are:
- Compare the two groups on changes in the daily minutes of physical activity (mild, moderate and vigorous) after sessions 1, 8 and 15, respectively (Sessions are typically one week a part. Due to holiday schedules, there may be a lapse of two weeks between sessions).
- Compare the two groups on changes in the daily minutes of sedentary behavior after sessions 1, 8 and 15, respectively
- Compare the two groups on changes in relative weight (weight, BMI percentile, BMI z-score) at sessions 1, 8, and 16 weeks, respectively
- Compare the two groups on measures of program satisfaction at 1, 8, and 16 weeks, respectively
Participation in the post session one session is required in order to be eligible for the study requirements include:
- A signed consent/ assent from the parent and child.
- The child must be able to participate in physical activity similar to exercise gaming
- The family must have a TV/monitor that supports Microsoft Kinect
- The family must have internet connection in the home
The family's decision to participate in the study does not affect the child's'/ parent's overall ability to fully participate in the JOIN Program. All JOIN program materials will be the same whether or not JOIN participants agree to be in the study. All aspects of the study will be conducted outside of the standard class time. Interested and eligible participants will be scheduled to attend a study visit immediately after their first JOIN class. During that study visit, written informed consent/assent from the parent/child will be obtained.
Once a participant has agreed to enroll and have been consented/assented he/she will be informed of study group to which he/she has been randomly assigned. There are two options: 1) weight management alone or 2) weight management plus exercise gaming and entertainment experience. Randomization will occur at the group level (i.e., all consented/assented children in the Wed at 5 p group). Classes will be randomized in pairs of 2 and based on enrollment.
Treatment JOIN consists of 16 weekly Core in-person group sessions followed by 8 monthly mastery group sessions. While the JOIN Program continues for one year, the study will only occur over the first 16 weeks. YMCA sessions last 75 minutes and include a weight assessment of the child prior to each session. The groups are led by a YMCA facilitator. The topics for the first 16 sessions are listed below.
Child Activity Monitor. At sessions 1, 8, and 15 an actigraph will be distributed to each participating child in group 1 and 2. Each child will wear it for 1 week (7 days) during waking hours, and return it at the next session. An activity monitor provides no feedback to participants and provides an objective measure of physical activity (mild, moderate, vigorous) as well as sedentary behavior through downloaded data. The GT3XE Triaxial Activity Monitor w/Extended Memory® (produced by Actigraph) is a small, omni-directional accelerometer (Actigraph), which has already been approved by the FDA for measuring subject's physical activity, and energy expenditure level. The activity monitor (Actigraph) is a small, 1 inch by 1 inch, device that is worn at the hip level attached to an adjustable belt (also provided by the study). The belt can be worn below or above clothing.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||77 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Evaluation of a Commercial Gaming Impact in a Childhood Obesity Intervention|
|Study Start Date :||August 2011|
|Primary Completion Date :||September 2012|
|Study Completion Date :||September 2012|
Experimental: Active Gaming
Participants will receivce a weight management program plus active gaming device
Behavioral: weight managment program
a comprehensive peditric weight management program consisting of 16 weekly group sessionsOther: Active Gaming
partcipants will be given a gaming device and 2 games (1 at baseline and 1 at week 8)
Other Name: Hands free Kinect gaming device plus 2 games
Active Comparator: Control Group
Participants will receive a weight management program without active gaming
Behavioral: weight managment program
a comprehensive peditric weight management program consisting of 16 weekly group sessions
- MVPA [ Time Frame: 16 weeks ]difference between groups in MVPA at week 16 as assess by accelerometry
- relative weight [ Time Frame: 16 weeks ]difference in % overweight, bmi z-score between groups at week 16
- quality of life [ Time Frame: 16 weeks ]Differences between groups in pediatric qulaitry of life as assessed by parents and children
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01757925
|United States, Massachusetts|
|Andover, Massachusetts, United States, 01810|
|Lawrence, Massachusetts, United States, 01840|
|YMCA Merrimack Valley of MAss|
|Methuen, Massachusetts, United States, 01844|
|Westborough, Massachusetts, United States, 01580|
|United States, Rhode Island|
|Barrington, Rhode Island, United States, 02806|
|Seakonk, Rhode Island, United States, 02771|
|Warwick, Rhode Island, United States, 02886|
|United States, Texas|
|Missouri City, Texas, United States, 77498|
|Barabara Jordan Elementary|
|Richmond, Texas, United States, 77407|
|Oyster Creek Elementary|
|Sugarland, Texas, United States, 77498|
|Sugraland, Texas, United States, 77498|