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Evaluating an In-home Multicomponent Program to Manage Concerns About Falling in Frail Community Dwelling Older People

9. juli 2012 opdateret af: Maastricht University Medical Center

Evaluating the Effectiveness of an In-home Self-management Intervention to Prevent Psychological Distress in Frail Older People Living in the Community

The main objectives of this study are:

  1. an effect evaluation of an in-home multicomponent cognitive behavioural program on concerns about falling and related avoidance of activity (primary outcomes), as well as disability, fall incidents (secondary outcomes) and several additional outcomes in frail community-dwelling older people,
  2. a process evaluation of the feasibility of the program, with the following main outcomes: population reached, performance according to protocol, exposure and engagement, opinion on the program of participants and facilitators, perceived benefit or achievement, and experienced barriers and potential solutions, and
  3. an economical evaluation on the impact of the program on healthcare utilization and related costs.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

389

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

      • Maastricht, Holland, 6221 GT
        • Maastricht University

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

70 år og ældre (Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Aged 70 years or over
  • At least some concerns about falling
  • At least some associated avoidance of activity
  • Fair or poor perceived general health
  • Living independently in the community
  • Written informed consent

Exclusion Criteria:

  • Cognitive impairment (a score of less than 4 on the Abbreviated Mental Test 4)
  • Language or hearing problems that impede completing an interview by telephone
  • Sight problems that impede completing the intervention
  • Confinement to bed
  • Waiting for nursing home admission
  • Permanent use of a wheelchair

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: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Cognitive behavioral program
an in-home cognitive behavioral program on managing concerns about falling and associated activity avoidance in frail community-dwelling older people facilitated by trained community nurses.
The in-home cognitive behavioral program aims to learn older persons, living in the community, how to deal with concerns about falling and to increase physical, social and functional activity. The principles of cognitive restructuring are used for shifting maladaptive in adaptive attitudes with respect to falling as well as increasing self efficacy beliefs and feelings of control. The following themes are discussed during the program: concerns about falling, thoughts about falling, physical exercise, assert oneself, overcome personal barriers, recognizing fall-ty habits and managing concerns about falling. Duration of the program is 10 weeks with 7 individual sessions (3 home visits (60, 60 and 75 minutes, respectively) & 4 telephone contacts (35 minutes each). The program is facilitated by trained nurses qualified in the field of geriatrics and working for home care agencies.
Ingen indgriben: Control group
no program, only care as usual

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
concerns about falling
Tidsramme: baseline, 5 months and 12 months
Falls Efficacy Scale International (FES-I)
baseline, 5 months and 12 months
avoidance of activities due concerns about falling
Tidsramme: baseline, 5 months and 12 months
Falls Efficacy Scale International Avoidance Behaviour (FES-IAB)
baseline, 5 months and 12 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
disability
Tidsramme: baseline, 5 months and 12 months
Groningen Activity Restriction Scale (GARS)
baseline, 5 months and 12 months
number of falls
Tidsramme: continuous registration during the course of the trial for a period of 1 year
Fall calendar
continuous registration during the course of the trial for a period of 1 year
catastrophic beliefs about falling
Tidsramme: baseline, 5 months and 12 months
Catastrophic beliefs about falling (CAFS)
baseline, 5 months and 12 months
perceived consequences of falling
Tidsramme: baseline, 5 months and 12 months
CoF - loss of functional independence subscale and damage to identity subscale
baseline, 5 months and 12 months
perceived control over falling
Tidsramme: baseline, 5 months and 12 months
Perceived control over falling (PCOF)
baseline, 5 months and 12 months
mastery
Tidsramme: baseline, 5 months and 12 months
Personal Mastery Scale
baseline, 5 months and 12 months
feelings of anxiety
Tidsramme: baseline, 5 months and 12 months
Subscale of the Hospital Anxiety and Depression Scale (HADS-A)
baseline, 5 months and 12 months
symptoms of depression
Tidsramme: baseline, 5 months and 12 months
Subscale of the Hospital Anxiety and Depression Scale (HADS-D)
baseline, 5 months and 12 months
social support interactions
Tidsramme: baseline, 5 months and 12 months
Social support interactions (SSL 12-I)
baseline, 5 months and 12 months
health-related quality of life
Tidsramme: baseline, 5 months and 12 months
SF-12 Health Survey
baseline, 5 months and 12 months

Samarbejdspartnere og efterforskere

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

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

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. marts 2009

Primær færdiggørelse (Faktiske)

1. maj 2011

Studieafslutning (Faktiske)

1. maj 2011

Datoer for studieregistrering

Først indsendt

17. maj 2011

Først indsendt, der opfyldte QC-kriterier

19. maj 2011

Først opslået (Skøn)

23. maj 2011

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

10. juli 2012

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. juli 2012

Sidst verificeret

1. juli 2012

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • MEC 07-3-064
  • ZonMw 120610001 (Andet bevillings-/finansieringsnummer: ZonMw 120610001)

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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