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Staying Healthy Through Education and Prevention Study (STEP)

Early Screening and Exercise for Prevention of Disability in Persons Residing in Continuing Care Retirement Communities

The purpose of this study is to test the effectiveness of a structured physical activity program, relative to a wellness program, in preventing the onset and progression of disability in the setting of senior housing communities, which are sometimes called housing with services.

Studieoversikt

Status

Ukjent

Forhold

Detaljert beskrivelse

As the baby boom population ages, a large number of older adults have found that continuing care retirement communities (CCRCs) offer an attractive residential option. These communities include independent apartments, assisted living and skilled nursing options and often provide a menu of wellness services and a "safety net" of higher level care if/when that care is needed. CCRCs have proliferated in recent years and the number of older adults selecting this residential option is expected to continue. CCRCs represent a largely untapped provider setting in which interventions that have been proven effective in clinically-oriented, controlled studies of community-dwelling elderly can be translated into practice.

Multiple randomized studies have shown the benefits of physical activity interventions such as resistance and endurance exercises on a number of performance measures including walking speed, balance and ability to stand from a chair. These studies have shown that if given an exercise program matched to their needs, the onset and progression of disability can be decreased among persons who are identified at high risk of disability. However, most data supporting the beneficial effect of exercise in old age have been generated from studies conducted in highly controlled clinical trial settings, not in "real world" provider settings in which older adults live and function day-to-day. Thus, it is not known if screening for disability and implementing an exercise program among high risk elders can be effectively implemented in residential settings in a manner that not only promotes health and prevents disability, but that is also attractive to providers from a business standpoint and that can be incorporated into typical staffing patterns.

The American Association of Homes & Services for the Aging (AAHSA) is conducting a trial that builds on a strong evidence base of the beneficial effect of exercise in old age in an effort to accelerate translation of research into practice in CCRCs. The trial will screen CCRC residents for disability using a short set of performance measures called the Short Physical Performance Battery (SPPB). After identification of persons at risk for disability, we will enroll 320 CCRC residents to a program of moderate exercise or an active control arm focused on general wellness. The primary study endpoint is the SPPB score. Secondary endpoints include falls; hospitalizations, and death.

A key feature of the current proposal is that it seeks to extend findings from clinical studies into routine practice in the CCRC setting. This represents true translation of research into practice, and will offer providers an evidence base upon which to make informed decisions.

The trial will take place in 8 CCRCs operated by the Good Samaritan Society, the largest nonprofit provider of services to older adults in the country. Because of its large size and existing dissemination capacity, Good Samaritan is in a unique position to take a leadership role among aging services providers in terms of dissemination of effective, innovative programs in diverse residential settings, including CCRCs.

Studietype

Intervensjonell

Registrering (Forventet)

320

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Arkansas
      • Mountain Home, Arkansas, Forente stater, 72653
        • Good Samaritan Society - Mountain Home
    • Colorado
      • Loveland, Colorado, Forente stater, 80537
        • Good Samaritan Society - Loveland Village
    • Florida
      • Deland, Florida, Forente stater, 32724
        • Good Samaritan Society - Florida Luthern
      • Kissimmee, Florida, Forente stater, 34746
        • Good Samaritan Society - Kissemmee Village
    • Kansas
      • Olathe, Kansas, Forente stater, 66061
        • Good Samaritan Society - Cedar Lake Village
    • Minnesota
      • Waconia, Minnesota, Forente stater, 55387
        • Good Samaritan Society - Westview Acres
    • Nebraska
      • Hastings, Nebraska, Forente stater, 68901
        • Good Samaritan Society - Hastings Village
    • New Mexico
      • Albuquerque, New Mexico, Forente stater, 87108
        • Good Samaritan Society - Manzano del Sol
    • Oregon
      • Gresham, Oregon, Forente stater, 97030
        • Good Samaritan Society - Fairlawn Village
    • Texas
      • Denton, Texas, Forente stater, 76201
        • Good Samaritan Society - Denton Village

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

65 år og eldre (Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Age ≥ 65
  • Currently reside in independent or assisted living units of participating senior housing with services communities and intend to stay at facility without interruption for the next year
  • Baseline SPPB scores between 3 and 9, inclusive.

Exclusion Criteria:

  • Age < 65
  • Severe cognitive impairment and/or inability to participate actively in the consent process (as determined by research staff).
  • Myocardial infarction, stroke, hip fracture, hip or knee replacement, major heart surgery, including valve replacement or bypass surgery, or blood clot in leg or lungs in the previous 3 months.
  • Self-reported inability to walk 13 feet with or without an assistive device
  • Refusal to participate in the consenting process
  • Failure to complete or attempt any of the 3 components of the SPPB for any non-physical reason
  • SPPB scores less than 3 or more than 9.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Physical Activity
Participants will begin to participate in walking sessions and strength building classes that will be offered at each location. Participants will be asked to attend a minimum of 1 strength class per week, with a target of doing 150 minutes of moderate exercise each week. The exercise classes will include stretching and counseling to help participants understand and address the barriers to becoming and staying involved in regular exercise.
Physical Activity program
Andre navn:
  • Trening
Aktiv komparator: Wellness
Participants will begin to participate in a wellness program that will meet at each site twice per month. The first meeting will involve a lecture or presentation on a wellness-related topic. The second meeting will follow-up on concepts that were introduced in the first meeting, and will also to provide participants an opportunity to share experiences. Participants will be asked to attend both wellness sessions each month for whole year that the program is running.
Wellness program
Andre navn:
  • Aktiv kontroll

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Short Physical Performance Battery score
Tidsramme: 12 months
12 months

Sekundære resultatmål

Resultatmål
Tidsramme
Incidence of Falls that result in participant being completely on the ground
Tidsramme: 12
12
Incidence of hospitalization
Tidsramme: 12 months
12 months
Incidence of Nursing home admission
Tidsramme: 12 months
12 months
Incidence of emergence room visit
Tidsramme: 12 months
12 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Helaine Resnick, PhD, American Association of Homes and Services for the Aging

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. januar 2009

Primær fullføring (Forventet)

1. september 2010

Studiet fullført (Forventet)

1. september 2010

Datoer for studieregistrering

Først innsendt

5. januar 2009

Først innsendt som oppfylte QC-kriteriene

5. januar 2009

Først lagt ut (Anslag)

6. januar 2009

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

28. mai 2010

Siste oppdatering sendt inn som oppfylte QC-kriteriene

27. mai 2010

Sist bekreftet

1. mai 2010

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • HHSA290200600024
  • 7581700 8-K72PS80 25505

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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