Multicomponent Exercise Training in Frail Elderly
Effectiveness of the Multicomponent Exercise Training in Frail Elderly
The aim of the present study will be to assess the effectiveness of the multicomponent exercise training in frail for the physical function, frailty and performance.
All the individuals will be assessed two times.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
This will be a experimental, randomized controlled intervention study in frail. Subjects will be recruited at the Albertia Care Center, Madrid. The exercise training group will developed a concurrent training 3 days per week during 6 weeks. The control group will follow an usual care also for 6 weeks.
The main variables will be as follows:
- Ultrasound imaging measurements for the lower limb: core muscles, vastus medialis, rectus femoris, vastus intermedius, gastrocnemius, soleus. We will employed a General Electric (GE) Ultrasound device in B mode to assess the thickness of the muscles.
- Heart rate variability with a Suunto smart bell.
- Activities of daily living with the Bartel index.
- Force-velocity profile and muscle power.
- Frailty with the Linda´s frailty criteria.
The exercise program was applied for 6 weeks. A total of 18 sessions were distributed in 3 weekly sessions. The participants performed a resistance exercises: leg press at an intensity of 40%-60% with 10 repetitions, 12 repetitions of steps with their bodyweight and a plantar flexion followed by a cardiovascular high intensity interval training (HIIT) exercise walking on a treadmill.
One measurements will be taken (pre), the second (post) measurements will be performed at 6 weeks.
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
-
Madrid, Spania
- Albertia Elderly Care Center
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- Men and women aged 75 years or more,
- 2 or more points in the Short Physical Performance Battery (SPPB)
- Capability of walking (alone or assisted)
Exclusion Criteria:
- Severity cognitive alterations
- Severe disability on the Barthel score
- Surgeries in the previous 6 months
- Other any disorder that exclude for the exercise group.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: Exercise program
The exercise program was applied for 6 weeks.
A total of 18 sessions were distributed in 3 weekly sessions.
The participants performed a resistance exercises: leg press at an intensity of 40%-60% with 10 repetitions, 12 repetitions of steps with their bodyweight and a plantar flexion followed by a cardiovascular HIIT exercise walking on a treadmill.
|
A multicomponent exercise program
|
|
Aktiv komparator: Daily activities
The patients who belongs to this group will continue to perform their daily routines.
|
A multicomponent exercise program
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Thickness of the core and quadriceps muscles
Tidsramme: Change from baseline muscle thickness at 6 weeks
|
Thickness assessment by ultrasound imaging
|
Change from baseline muscle thickness at 6 weeks
|
|
Heart rate variability
Tidsramme: Change from baseline heart rate variability at 6 weeks
|
Heart rate variability by Suunto smart bell device
|
Change from baseline heart rate variability at 6 weeks
|
|
Daily life activities
Tidsramme: Change from baseline daily life activities at 6 weeks
|
Bartel index questionnaire
|
Change from baseline daily life activities at 6 weeks
|
|
Muscle power
Tidsramme: Change from baseline muscle power at 6 weeks
|
Force-velocity profile for the lower limb muscle power
|
Change from baseline muscle power at 6 weeks
|
|
Frailty
Tidsramme: Change from baseline frailty at 6 weeks
|
Frailty with the Linda´s frailty criteria
|
Change from baseline frailty at 6 weeks
|
Samarbeidspartnere og etterforskere
Sponsor
Etterforskere
- Hovedetterforsker: Sergio López, MsC, Universidad Europea de Madrid
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- CIPI/
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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. .