Evaluation of a Commercial Gaming Impact in a Childhood Obesity Intervention

Sponsor
UnitedHealth Group (Industry)
Overall Status
Completed
CT.gov ID
NCT01757925
Collaborator
(none)
77
11
2
13
7
0.5

Study Details

Study Description

Brief Summary

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
  • Behavioral: weight managment program
  • Other: Active Gaming
Phase 4

Detailed Description

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 Design

Study Type:
Interventional
Actual Enrollment :
77 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluation of a Commercial Gaming Impact in a Childhood Obesity Intervention
Study Start Date :
Aug 1, 2011
Actual Primary Completion Date :
Sep 1, 2012
Actual Study Completion Date :
Sep 1, 2012

Arms and Interventions

Arm Intervention/Treatment
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 sessions

Other: Active Gaming
partcipants will be given a gaming device and 2 games (1 at baseline and 1 at week 8)
Other Names:
  • 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

    Outcome Measures

    Primary Outcome Measures

    1. MVPA [16 weeks]

      difference between groups in MVPA at week 16 as assess by accelerometry

    Secondary Outcome Measures

    1. relative weight [16 weeks]

      difference in % overweight, bmi z-score between groups at week 16

    2. quality of life [16 weeks]

      Differences between groups in pediatric qulaitry of life as assessed by parents and children

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    6 Years to 12 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Children ages 6 - 12 with Parent or Gaurdian.

    • Child must be enroll in JOIN Program,

    • Child must have a BMI in the 85th percentile

    Exclusion Criteria:
    • English Speaking Participants only

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 YMCA Andvore Andover Massachusetts United States 01810
    2 YMCA Lawrence Lawrence Massachusetts United States 01840
    3 YMCA Merrimack Valley of MAss Methuen Massachusetts United States 01844
    4 YMCA Boroughs Westborough Massachusetts United States 01580
    5 Barrinton YMCA Barrington Rhode Island United States 02806
    6 Newman YMCA Seakonk Rhode Island United States 02771
    7 YMCA Kent Warwick Rhode Island United States 02886
    8 Jones Elementary Missouri City Texas United States 77498
    9 Barabara Jordan Elementary Richmond Texas United States 77407
    10 Oyster Creek Elementary Sugarland Texas United States 77498
    11 Townwest Elementary Sugraland Texas United States 77498

    Sponsors and Collaborators

    • UnitedHealth Group

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dr. Deneen Vojta, Dr. Deneen Vojta Vice President of Center for Health Reform and Modernization, UnitedHealth Group
    ClinicalTrials.gov Identifier:
    NCT01757925
    Other Study ID Numbers:
    • JXBX 2012 11-214
    First Posted:
    Dec 31, 2012
    Last Update Posted:
    Dec 31, 2012
    Last Verified:
    Dec 1, 2012
    Keywords provided by Dr. Deneen Vojta, Dr. Deneen Vojta Vice President of Center for Health Reform and Modernization, UnitedHealth Group
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 31, 2012