- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01247636
Home-Exercise vs General Physical Activity: Effect on Health-related Quality of Life
23. november 2010 opdateret af: Oslo University Hospital
Effect of Progressive Home-Exercise on Health-related Quality of Life, Balance and Mobility in Older People Discharge From an Outpatient Geriatric Clinic.
The purpose of this randomized controlled trial is to evaluate the effectiveness of an exercised-based programme developed for older people admitted at a geriatric outpatient clinic and to see if a home-exercise program enhances the effect.
The outcomes considered is health-related quality of life, balance-self confidence, balance and mobility.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Older people discharge from hospital often have decreased functional and physiological reserve that make them vulnerable of being dependent of others.
Research have shown that older people discharge from hospital are vulnerable for functional decline during hospital stay and this decline can persist 6 to 18 months after discharge from hospital.Exercise interventions are proven to have effect on mobility, balance and falls among community-dwelling older people and several studies have shown that deconditioning as a consequence of disuse is reversible with training even in very old individuals.
However, few studies have evaluated the effects of physical activity promotion and exercise intervention among elderly recently discharge from a geriatric outpatient clinic.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
110
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Oslo, Norge
- Ullevål University Hospital
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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
60 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- home-dwelling patients who were admitted at the geriatric clinic.
- Assessed by a doctor to tolerate training
- Able to walk in the corridor for 3 min with or without assistive device
Exclusion Criteria:
- Cognitive disorders mini mental status < 24
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: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Home-exercise
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Balance-training admitted at the geriatric hospital Home-exercise or advice to be generally active
Andre navne:
The aim of the intervention was to enhance health-related quality of life, self-efficacy and physical function through education and exercise.
The education program consisted of information given both oral and in writing regarding the benefits of physical activity.
The aim was to increase the participants knowledge about the benefits of physical activity and to stimulate them to integrate physical activity into their immediate environment during daily routines.
They were given an exercise-log and were advised to write down all their daily activities and exercise.
The exercise program were conducted 2 times per week for 45 min per session.
The content of these sessions were balance training with main focus on balance-exercises considered essential for daily living.
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Sundhedsrelateret livskvalitet
Tidsramme: 3 måneder
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3 måneder
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Health-related quality of life
Tidsramme: by the time of discharge mean 2 weeks after admission
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by the time of discharge mean 2 weeks after admission
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Functional balance (Berg Balance Scale)
Tidsramme: by the time of discharge mean 2 weeks after admission and after 3 months
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by the time of discharge mean 2 weeks after admission and after 3 months
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Functional mobility
Tidsramme: by the time of discharge mean 2 weeks after admission, and after 3 months
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Timed up and go test and 6 min walk test
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by the time of discharge mean 2 weeks after admission, and after 3 months
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Functional strength
Tidsramme: by the time of discharge mean 2 weeks after admission and after 3 months
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by the time of discharge mean 2 weeks after admission and after 3 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Studiestol: Astrid Bergland, Professor, No afflication
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. januar 2005
Primær færdiggørelse (Faktiske)
1. januar 2007
Studieafslutning (Faktiske)
1. januar 2007
Datoer for studieregistrering
Først indsendt
18. november 2010
Først indsendt, der opfyldte QC-kriterier
23. november 2010
Først opslået (Skøn)
24. november 2010
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
24. november 2010
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
23. november 2010
Sidst verificeret
1. januar 2005
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- S-03247
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 .