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PlayFit Pilot: Encouraging Social Physical Play in the Community

6. Dezember 2016 aktualisiert von: 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.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Tatsächlich)

8

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

  • Vereinigte Staaten
    • Pennsylvania
      • Hershey, Pennsylvania, Vereinigte Staaten, 17033
        • Penn State Hershey Medical Center

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

21 Jahre bis 50 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

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)

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
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.
Verhalten: PlayFit - 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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Compare exercise intensity, METS (Metabolic Equivalent Task)
Zeitfenster: 12 weeks
METS will be measured during each exercise session using an accelerometer (ActiGraph GT3X).
12 weeks

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Self-reported weight
Zeitfenster: 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
Zeitfenster: 12 weeks
Self-reported height will be captured by a research assistant at baseline and follow up (12 week) visits.
12 weeks
Gender
Zeitfenster: 12 weeks
Participants will be asked if they are male or female.
12 weeks
Self-reported chronic conditions
Zeitfenster: 12 weeks
Participants will be asked 4 questions on which chronic conditions (if any) they may have.
12 weeks
Ethnicity
Zeitfenster: 12 weeks
Participants will be asked what their ethnicity is.
12 weeks
Race
Zeitfenster: 12 weeks
Participants will be asked what their race is.
12 weeks
Education Level
Zeitfenster: 12 weeks
Participants will be asked 1 question on education level.
12 weeks
Employment Status
Zeitfenster: 12 weeks
Participants will be asked 1 question on employment status.
12 weeks
Tobacco Use
Zeitfenster: 12 weeks
Participants will be asked 1 question on tobacco use.
12 weeks
National Health Interview Survey
Zeitfenster: 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
Zeitfenster: 12 weeks
Participants will be asked 1 question on their overall health.
12 weeks
Three Item Loneliness Scale
Zeitfenster: 12 weeks
Participants will be asked 3 questions on feelings of being lonely.
12 weeks
Patient Reported Outcomes (PROMIS) - Anxiety
Zeitfenster: 12 weeks
Participants will be asked questions 4 questions on anxiety.
12 weeks
Patient Reported Outcomes (PROMIS) - Depression
Zeitfenster: 12 weeks
Participants will be asked 4 questions on Depression.
12 weeks
Patient Reported Outcomes (PROMIS) - Physical Function
Zeitfenster: 12 weeks
Participants will be asked 4 questions on physical function.
12 weeks
Sport playing status
Zeitfenster: 12 weeks
Participants will be asked 2 questions on playing sports previously.
12 weeks
Program Intensity Survey
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Milton S. Hershey Medical Center

Ermittler

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

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. August 2016

Primärer Abschluss (Tatsächlich)

1. November 2016

Studienabschluss (Tatsächlich)

1. November 2016

Studienanmeldedaten

Zuerst eingereicht

17. Oktober 2016

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

24. Oktober 2016

Zuerst gepostet (Schätzen)

25. Oktober 2016

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

8. Dezember 2016

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

6. Dezember 2016

Zuletzt verifiziert

1. Dezember 2016

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Zusätzliche relevante MeSH-Bedingungen

Andere Studien-ID-Nummern

  • 4785

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