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PlayFit Pilot: Encouraging Social Physical Play in the Community

6. december 2016 opdateret af: 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.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

8

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

  • Forenede Stater
    • Pennsylvania
      • Hershey, Pennsylvania, Forenede Stater, 17033
        • Penn State Hershey Medical Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

21 år til 50 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

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)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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.
Adfærdsmæssigt: 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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Compare exercise intensity, METS (Metabolic Equivalent Task)
Tidsramme: 12 weeks
METS will be measured during each exercise session using an accelerometer (ActiGraph GT3X).
12 weeks

Sekundære resultatmål

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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Milton S. Hershey Medical Center

Efterforskere

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

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. august 2016

Primær færdiggørelse (Faktiske)

1. november 2016

Studieafslutning (Faktiske)

1. november 2016

Datoer for studieregistrering

Først indsendt

17. oktober 2016

Først indsendt, der opfyldte QC-kriterier

24. oktober 2016

Først opslået (Skøn)

25. oktober 2016

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

8. december 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

6. december 2016

Sidst verificeret

1. december 2016

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • 4785

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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