- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02832466
Quantifying the Deterioration of Physical Function in Renal Patients
Quantifying the Deterioration of Physical Function Along 6 Months in Patients in End Stage Renal Disease
Patients undergoing haemodialysis present a decrease in physical function, but little is known about the rate at which function decreases.
The purpose of this study is quantifying the nature and degree of functional deterioration experienced by stage 5 chronic kidney disease patients during a six month period of maintenance haemodialysis therapy.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Contatti e Sedi
Luoghi di studio
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Valencia
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Moncada, Valencia, Spagna, 46113
- Universidad CEU Cardenal Herrera
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Metodo di campionamento
Popolazione di studio
Descrizione
Inclusion Criteria:
- people under hemodialysis treatment at least 3 months
- be medicable stable
- complete all the physical tests
Exclusion Criteria:
- heart stroke in the previous 6 weeks of the study
- inferior limb amputation without artificial aids
- cerebral vascular disease (ictus, ischemic)
- disability to complete functional tests
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change from Baseline Short Physical Performance Battery at 6 months
Lasso di tempo: At the beginning of the study and after 6 months
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Assess lower extremity, which includes objective performance-based measure of balance (side-by-side, semi-tanden and tandem), endurance (4m gait speed) and strength (five chair stands).
Each component was scored from 0 to 4 and when summed yielded Short Physical Performance Battery scores between 0 (poor) and 12 (best).
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At the beginning of the study and after 6 months
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Change from Baseline One Leg Standing Test at 6 months
Lasso di tempo: At the beginning of the study and after 6 months
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Consist in maintain one leg stance for as long as possible.
The test was considered normal if the one leg standing time reached 45 seconds.
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At the beginning of the study and after 6 months
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Change from Baseline Timed Up and Go at 6 months
Lasso di tempo: At the beginning of the study and after 6 months
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To stand up from a standard arms chair, walk 3 meters, turn back the cone walk back and sit down to the chair.
The time in seconds is record.
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At the beginning of the study and after 6 months
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Change from Baseline Sit to Stand to Sit 10 and 60 at 6 months
Lasso di tempo: At the beginning of the study and after 6 months
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For the Sit To Stand 10 participant has to stand up and sit down 10 times and the time needed is record; while for the Sit to stand to sit 60 the participant consist in measures how many repetition the participant can to stand up and sit down during 60 seconds
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At the beginning of the study and after 6 months
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Change from Baseline On leg heel rise at 6 months
Lasso di tempo: At the beginning of the study and after 6 months
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It measures the strength in the triceps surae in the one leg standing position and has to rise the heel.
It measures how many repetitions the participants is can do
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At the beginning of the study and after 6 months
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Change from Baseline Handgrip strength at 6 months
Lasso di tempo: At the beginning of the study and after 6 months
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To measure the amount of strength developed by each hand in kg
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At the beginning of the study and after 6 months
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Change from Baseline Six Minutes Walking Time at 6 months
Lasso di tempo: At the beginning of the study and after 6 months
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To walk the longest distance possible in 6 minutes by walking continuously the 20 or 30 metres indicated on the floor.
It measures the distance in meters
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At the beginning of the study and after 6 months
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Eva Segura Ortí, Lecturer in the Cardenal Herrera University
Studiare le date dei record
Studia le date principali
Inizio studio
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- Cardenal Herrera Univeristy
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .