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Functional Impact of a Memory Intervention Program

12. januar 2016 oppdatert av: Susan Vandermorris, Ph.D., C.Psych., Baycrest

Normal aging is associated with decline in some aspects of memory, and this can be a risk factor for reductions in everyday functioning. The Baycrest Memory and Aging Program teaches positive adaptation to age-related memory changes, including strategies for minimizing the everyday impact of normal memory change and positive lifestyle change to maximize brain health. Prior research has shown that the Memory and Aging program is effective in increasing participants' knowledge about memory, use of memory strategies, and confidence in memory function, as well as adoption of healthier lifestyle practices and reduction in intention to use unneeded health care resources.

Although not one of the stated goals of the program, informal feedback from participants suggests that the educational content and skills training in the Memory and Aging Program has led some participants to change behaviours in ways that lead to significant improvements in their everyday functioning. For example, graduating participants often volunteer examples of how they have applied what they have learned to succeed in everyday memory tasks such as learning a new name or keeping track of future plans. Based on this participant feedback, it is hypothesized that the knowledge, skills, and confidence gained by Memory and Aging Program participants may lead to positive behaviour changes that, in turn, lead to improved everyday functioning. The present study will test this hypothesis using a randomized controlled pretest-posttest design.

Studieoversikt

Status

Fullført

Forhold

Studietype

Intervensjonell

Registrering (Faktiske)

69

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

    • Ontario
      • Toronto, Ontario, Canada, M6A 2E1
        • Baycrest

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

50 år til 90 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • Age 50-90
  • Available to participate in all testing and intervention sessions (located in Toronto, Canada)

Exclusion Criteria:

  • health conditions with major effects on cognition, including a current or previous history of stroke, brain surgery, or diagnosed neurological disorder
  • dependence in instrumental activities of daily living
  • cognitive impairment, defined as performance below cutoff for cognitive impairment on a standardized cognitive test, the Telephone Interview for Cognitive Status (Brandt, Spencer, & Folstein, 1988).
  • affective impairment, defined as performance below cutoff for depression on standardized depression screen, the Geriatric Depression Scale (Yesavage et al., 1983)

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Memory and Aging Program
The Memory and Aging Program intervention consists of five 2-hour sessions conducted over five consecutive weeks. The content of the program includes: (a) the provision of factual information (i.e., about memory, age-related memory changes, lifestyle factors affecting memory, and memory strategies) in an informal lecture format; and (b) memory intervention (i.e., practice and application of several evidence-based memory strategies) in a hands-on interactive format.
Ingen inngripen: Wait-list Control
Participants randomized to the wait-list control group will receive no intervention following randomization. They will be offered the intervention immediately following completion of the week 14 outcome testing session.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Change from baseline in healthy lifestyle behaviours as measured by Health Promoting Lifestyle Profile II (Walker, Sechrist, & Pender, 1987)
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14
Change from baseline in memory strategy use as measured by the Memory Strategy Toolbox (modified from Troyer, 2001)
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14
Attainment of individualized goals for (a) lifestyle change, (b) memory strategy use, and (c) functional outcomes of memory strategy use as measured by Goal Attainment Scaling (Gordon, Powell, & Rockwood, 2000; Kiresuk, Smith, & Cardillo, 1994)
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14

Sekundære resultatmål

Resultatmål
Tidsramme
Change in positive and negative affect as measured by Positive and Negative Affect Schedule (Watson, Clark, & Tellegen, 1988)
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14
Change in general health status as measured by the RAND 36-Item Short-Form Health Survey (Ware & Sherbourne, 1992).
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14
General Self-Efficacy Scale (Schwarzer & Jerusalem, 1995)
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14
Prospective and Retrospective Memory Questionnaire (Smith, Della Sala, Logie, & Maylor, 2000)
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14
Self-report health status, lifestyle changes, attitudes about aging
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14

Andre resultatmål

Resultatmål
Tidsramme
Change in memory knowledge as measured by Memory knowledge quiz (modified from Troyer, 2001).
Tidsramme: Baseline, Week 8, week 14
Baseline, Week 8, week 14
Change in self-perceived memory as measured by Multifactorial Metamemory Questionnaire (Troyer & Rich, 2002)
Tidsramme: Baseline, 8 weeks, 14 weeks
Baseline, 8 weeks, 14 weeks
Change in prospective memory function (Prospective telephone-call task, Troyer, 2001; actual week, Rendell & Craik, 2001)
Tidsramme: Baseline, 8 weeks, 14 weeks
Baseline, 8 weeks, 14 weeks
Change in name learning (Name-learning task, based on Troyer, Häfliger, Cadieux, & Craik, 2006)
Tidsramme: Baseline, 8 weeks, 14 weeks
Baseline, 8 weeks, 14 weeks

Samarbeidspartnere og etterforskere

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

Sponsor

Etterforskere

  • Hovedetterforsker: Susan Vandermorris, PhD, Baycrest

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.

Generelle publikasjoner

Hjelpsomme linker

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. mai 2014

Primær fullføring (Faktiske)

1. oktober 2015

Studiet fullført (Faktiske)

1. oktober 2015

Datoer for studieregistrering

Først innsendt

12. mars 2014

Først innsendt som oppfylte QC-kriteriene

12. mars 2014

Først lagt ut (Anslag)

14. mars 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

13. januar 2016

Siste oppdatering sendt inn som oppfylte QC-kriteriene

12. januar 2016

Sist bekreftet

1. januar 2016

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 14-21

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. .

Kliniske studier på Memory and Aging Program

3
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