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CompletedNCT02944370Updated Dec 8, 2016

PlayFit Pilot: Encouraging Social Physical Play in the Community

An interventional study of PlayFit - modified exercise games in Overweight and Obesity, sponsored by Milton S. Hershey Medical Center. Completed at 1 site in United States. Open to participants aged 21 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-12-08.

Sponsored by Milton S. Hershey Medical Center · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
8
Allocation
Not applicable
Ages
21 Years to 50 Years
Sex
All
01

Study summary

The investigator is pilot testing the feasibility and impact of a low-cost intervention that uses existing gymnasiums, and therefore has the potential to be replicated across the United States. The intervention, PlayFit, is designed for adults aged 21-50. PlayFit has five key components, intended to overcome the major barriers to physical activity. First, it will assist people in finding others to play with, using the Pick-Up model of designating times to play and making those times known in the community. Second, it will overcome a lack of confidence in physical activity by including games of lower intensity for relatively unfit adults, then building up to moderate and vigorous games. Third, it will require team members of varying ages and genders to encourage intergenerational play. Fourth, it will use modified equipment (e.g., softer, lighter balls) and smaller game space to require less running, so that even relatively unfit people can feel confident participating. Fifth, it will be designed to be led by community volunteers, which will increase its disseminability.

AIM - Understand the optimum design for PlayFit. To meet this aim, the investigators will come up with a list of games to play and pilot the games at a gymnasium. The investigators will observe the participants playing the games and have them complete a brief survey.

02

Conditions studied

  • Overweight and Obesity
03

In context

Overweight

3,767 studies on the registry are indexed under Overweight; 863 are open to participants now.

This study's enrollment of 8 is below the median of 73 across 3,263 interventional studies indexed under Overweight.

Browse Overweight studies →

Lead sponsor

Milton S. Hershey Medical Center is the lead sponsor of 491 studies on the registry; 59 are open to participants now.

Of its 58 completed or terminated interventional studies of FDA-regulated products, 44 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
21 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 21-50
  • Fluently read and speak English
  • Current member of Hershey Medical Center's University Fitness Center OR willing to become a member
  • Currently exercises \< 150 minutes per week

Exclusion criteria

Exclusion Criteria:

  • Has been told by a doctor they a heart condition and should only do exercise recommended by a doctor
  • Currently pregnant or planning to become pregnant in the next 6 months
  • Planning to move out of the area in the next 6 months
  • Has pain in chest, neck, jaw, or arms at rest, during daily activities of living
  • Has experienced a forceful or rapid heart rate
  • Has experience unreasonable breathlessness
  • Has experienced dizziness fainting or blackouts
  • Has experienced ankle swelling
  • Has burning or cramping sensation in lower legs when walking short distances
  • Has been told by a health professional not to exercise OR exercise only when supervised by a professional
  • Has been diagnosed with diabetes
  • Has been told by a doctor, nurse or health professional that they have (1) Weak or failing kidneys, (2) A heart attack/ myocardial infarction, (3) Angina or coronary heart disease, (4) A stroke, or (5) Any other kind of heart condition or heart disease - e.g. heart valve problem/aortic regurgitation (do not include heart murmur)
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
8 participants (actual)

Study arms

  • Experimental
    PlayFit, Modified exercise games

    Subjects will participate in three 60 minute game sessions each week for 12 weeks. During each game session, subjects will be divided randomly into two teams to play a modified game. Research staff will review the instructions of the game and if needed, modify the game rules during play to enhance the experience (ie. keep it fun, keep it to moderate intensity level). The length of play session between breaks increases each week.

    Behavioral: PlayFit - modified exercise games

Interventions

  • BehavioralPlayFit - modified exercise games

    Play modified games with other adults three times a week for 12 weeks. Complete a brief survey on the games played and program satisfaction.

06

What researchers measure

Primary outcomes

  1. Compare exercise intensity, METS (Metabolic Equivalent Task)

    METS will be measured during each exercise session using an accelerometer (ActiGraph GT3X).

    Time frame: 12 weeks

Secondary outcomes

  1. Self-reported weight

    Self-reported weight will be captured by a research assistant at baseline and follow up (12 week) visits.

    Time frame: 12 weeks

  2. Self-reported height

    Self-reported height will be captured by a research assistant at baseline and follow up (12 week) visits.

    Time frame: 12 weeks

  3. Gender

    Participants will be asked if they are male or female.

    Time frame: 12 weeks

  4. Self-reported chronic conditions

    Participants will be asked 4 questions on which chronic conditions (if any) they may have.

    Time frame: 12 weeks

  5. Ethnicity

    Participants will be asked what their ethnicity is.

    Time frame: 12 weeks

  6. Race

    Participants will be asked what their race is.

    Time frame: 12 weeks

  7. Education Level

    Participants will be asked 1 question on education level.

    Time frame: 12 weeks

  8. Employment Status

    Participants will be asked 1 question on employment status.

    Time frame: 12 weeks

  9. Tobacco Use

    Participants will be asked 1 question on tobacco use.

    Time frame: 12 weeks

  10. National Health Interview Survey

    Participants will be asked 2 questions from this survey on how difficult it is to walk and carry an item.

    Time frame: 12 weeks

  11. General Self Rated Health

    Participants will be asked 1 question on their overall health.

    Time frame: 12 weeks

  12. Three Item Loneliness Scale

    Participants will be asked 3 questions on feelings of being lonely.

    Time frame: 12 weeks

  13. Patient Reported Outcomes (PROMIS) - Anxiety

    Participants will be asked questions 4 questions on anxiety.

    Time frame: 12 weeks

  14. Patient Reported Outcomes (PROMIS) - Depression

    Participants will be asked 4 questions on Depression.

    Time frame: 12 weeks

  15. Patient Reported Outcomes (PROMIS) - Physical Function

    Participants will be asked 4 questions on physical function.

    Time frame: 12 weeks

  16. Sport playing status

    Participants will be asked 2 questions on playing sports previously.

    Time frame: 12 weeks

  17. Program Intensity Survey

    Participants will be asked 2 questions after each game session on how physically and technically hard the game was.

    Time frame: 12 weeks

  18. Program Satisfaction Survey

    Participants will be asked 2 questions after each game session on what they did and did not like about the game.

    Time frame: 12 weeks

  19. Net Promoter Score

    Participants will be asked 1 question on how likely they would recommend the day's activity/game to a friend or family member.

    Time frame: 12 weeks

07

Study locations

1 site
  • Penn State Hershey Medical Center
    Hershey, Pennsylvania 17033, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 8, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02944370
Responsible party
Christopher Sciamanna, MD, MPH (Professor of Medicine, Division Chief of Population Health, Research and Development, Milton S. Hershey Medical Center) — Principal investigator
First posted
Oct 25, 2016
Start date
Aug 2016
Primary completion
Nov 2016
Completion
Nov 2016
Last update
Dec 8, 2016

Study contacts

Christopher Sciamanna, MD, MPH
principal investigator · Milton S. Hershey Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2016. You cannot join it, but the record below documents what was studied.

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