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PlayFit Pilot: Encouraging Social Physical Play in the Community

PlayFit Pilot: Encouraging Social Physical Play in the Community

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02944370
Enrollment
8
Registered
2016-10-25
Start date
2016-08-31
Completion date
2016-11-30
Last updated
2016-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight and Obesity

Brief 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.

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.

Sponsors

Milton S. Hershey Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 50 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Compare exercise intensity, METS (Metabolic Equivalent Task)12 weeksMETS will be measured during each exercise session using an accelerometer (ActiGraph GT3X).

Secondary

MeasureTime frameDescription
Self-reported height12 weeksSelf-reported height will be captured by a research assistant at baseline and follow up (12 week) visits.
Gender12 weeksParticipants will be asked if they are male or female.
Self-reported chronic conditions12 weeksParticipants will be asked 4 questions on which chronic conditions (if any) they may have.
Ethnicity12 weeksParticipants will be asked what their ethnicity is.
Race12 weeksParticipants will be asked what their race is.
Education Level12 weeksParticipants will be asked 1 question on education level.
Employment Status12 weeksParticipants will be asked 1 question on employment status.
Tobacco Use12 weeksParticipants will be asked 1 question on tobacco use.
National Health Interview Survey12 weeksParticipants will be asked 2 questions from this survey on how difficult it is to walk and carry an item.
Self-reported weight12 weeksSelf-reported weight will be captured by a research assistant at baseline and follow up (12 week) visits.
Three Item Loneliness Scale12 weeksParticipants will be asked 3 questions on feelings of being lonely.
Patient Reported Outcomes (PROMIS) - Anxiety12 weeksParticipants will be asked questions 4 questions on anxiety.
Patient Reported Outcomes (PROMIS) - Depression12 weeksParticipants will be asked 4 questions on Depression.
Patient Reported Outcomes (PROMIS) - Physical Function12 weeksParticipants will be asked 4 questions on physical function.
Sport playing status12 weeksParticipants will be asked 2 questions on playing sports previously.
Program Intensity Survey12 weeksParticipants will be asked 2 questions after each game session on how physically and technically hard the game was.
Program Satisfaction Survey12 weeksParticipants will be asked 2 questions after each game session on what they did and did not like about the game.
Net Promoter Score12 weeksParticipants will be asked 1 question on how likely they would recommend the day's activity/game to a friend or family member.
General Self Rated Health12 weeksParticipants will be asked 1 question on their overall health.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026