PlayFit Pilot: Encouraging Social Physical Play in the Community

December 6, 2016 updated by: Christopher Sciamanna, MD, MPH, Milton S. Hershey Medical Center

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.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

8

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

    • Pennsylvania
      • Hershey, Pennsylvania, United States, 17033
        • Penn State Hershey Medical Center

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

21 years to 50 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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:

  • 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)

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: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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.
Play modified games with other adults three times a week for 12 weeks. Complete a brief survey on the games played and program satisfaction.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Compare exercise intensity, METS (Metabolic Equivalent Task)
Time Frame: 12 weeks
METS will be measured during each exercise session using an accelerometer (ActiGraph GT3X).
12 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported weight
Time Frame: 12 weeks
Self-reported weight will be captured by a research assistant at baseline and follow up (12 week) visits.
12 weeks
Self-reported height
Time Frame: 12 weeks
Self-reported height will be captured by a research assistant at baseline and follow up (12 week) visits.
12 weeks
Gender
Time Frame: 12 weeks
Participants will be asked if they are male or female.
12 weeks
Self-reported chronic conditions
Time Frame: 12 weeks
Participants will be asked 4 questions on which chronic conditions (if any) they may have.
12 weeks
Ethnicity
Time Frame: 12 weeks
Participants will be asked what their ethnicity is.
12 weeks
Race
Time Frame: 12 weeks
Participants will be asked what their race is.
12 weeks
Education Level
Time Frame: 12 weeks
Participants will be asked 1 question on education level.
12 weeks
Employment Status
Time Frame: 12 weeks
Participants will be asked 1 question on employment status.
12 weeks
Tobacco Use
Time Frame: 12 weeks
Participants will be asked 1 question on tobacco use.
12 weeks
National Health Interview Survey
Time Frame: 12 weeks
Participants will be asked 2 questions from this survey on how difficult it is to walk and carry an item.
12 weeks
General Self Rated Health
Time Frame: 12 weeks
Participants will be asked 1 question on their overall health.
12 weeks
Three Item Loneliness Scale
Time Frame: 12 weeks
Participants will be asked 3 questions on feelings of being lonely.
12 weeks
Patient Reported Outcomes (PROMIS) - Anxiety
Time Frame: 12 weeks
Participants will be asked questions 4 questions on anxiety.
12 weeks
Patient Reported Outcomes (PROMIS) - Depression
Time Frame: 12 weeks
Participants will be asked 4 questions on Depression.
12 weeks
Patient Reported Outcomes (PROMIS) - Physical Function
Time Frame: 12 weeks
Participants will be asked 4 questions on physical function.
12 weeks
Sport playing status
Time Frame: 12 weeks
Participants will be asked 2 questions on playing sports previously.
12 weeks
Program Intensity Survey
Time Frame: 12 weeks
Participants will be asked 2 questions after each game session on how physically and technically hard the game was.
12 weeks
Program Satisfaction Survey
Time Frame: 12 weeks
Participants will be asked 2 questions after each game session on what they did and did not like about the game.
12 weeks
Net Promoter Score
Time Frame: 12 weeks
Participants will be asked 1 question on how likely they would recommend the day's activity/game to a friend or family member.
12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Christopher Sciamanna, MD, MPH, Milton S. Hershey Medical Center

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

August 1, 2016

Primary Completion (Actual)

November 1, 2016

Study Completion (Actual)

November 1, 2016

Study Registration Dates

First Submitted

October 17, 2016

First Submitted That Met QC Criteria

October 24, 2016

First Posted (Estimate)

October 25, 2016

Study Record Updates

Last Update Posted (Estimate)

December 8, 2016

Last Update Submitted That Met QC Criteria

December 6, 2016

Last Verified

December 1, 2016

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 4785

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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