- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01577927
Feasibility Study of a Home Rehabilitative Network to Treat Prolonged Weaned Patients (UTIR)
Feasibility and Efficacy of a Home Rehabilitative Network for Prolonged Weaned Patients Discharged From a Weaning Unit
Patients at high complexity with severe chronic diseases can require several admission in intensive care units (ICU) to overcome acute exacerbations by the use of assisted ventilation. In the last 10 years, new technologies and beds in ICU evidenced a new group of patients often needing weaning procedures due to a long-lasting period of mechanical ventilation. These patients are often under chronic conditions with recurrent symptoms, reduced effort tolerance and depression.
Weaning process is a frail step in the medical history of a patient who has survived an acute episode of respiratory failure and has spent a period of time under mechanical ventilation. Patients are followed for the duration of in-hospital stay, an expected average period of 4 weeks.
When discharged fron an Intensive Care Unit (ICU) or a weaning center, the patient is usually managed by GPs and by the hospital where he has been admitted to following re-exacerbations. The conventional approach is for sure inadequate for this type of patient whose clinical complexity, disability and frailty need for a continuity of care through a higher complex approach of management.
A structured program of Home Rehabilitation could be a possible solution to this problem. Thus, the hypothesis of the study is to evaluate feasibility and sustainability and efficacy of a home rehabilitative network for prolonged weaned patients discharged from a weaning unit.
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
-
Brescia
-
Lumezzane, Brescia, Italien, 25065
- Fondazione Salvatore Maugeri
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
- General Inclusion criteria: 1. Signature of the informed 2. Good expectation of life
- Specific Inclusion Criteria : Score of general dependences < 19 according to the Critical Patients Autonomy Planning (CPAP) Scale
Exclusion Criteria:
- Patient with neuromuscular, highly progressive neurological diseases (i.e. amyotrophic lateral sclerosis), patient requiring surgical interventions, sedation, and hemodialysis.
- Unstable patient conditions as daily variability of the blood arterial pressure >20%, arrhythmias, PaO2/FiO2 < 300, unsatisfactory respiratory pattern, haemoglobin < 7 g /dL, temperature > 38°C, presence of neurological or orthopaedic side effects, and recent embolisms from TVP. Refusal.
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Stödjande vård
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Aktiv komparator: Usual home care
No assistance or care by PT.
|
Usual home care consists in supporting drug and oxygen therapy, mechanical ventilation, GP's assistance,and periodical in-hospital visit.
|
|
Experimentell: PT-assisted home rehabilitation
Assisted home care is supported by a PT at least 2 times/month.
Few brief educational lessons preceeded the training activity that the patient performs by himself at home.
|
Patient performs 50 min physical activity/working day autonomously by the help of a DVD. The physical activity consists in cyclette, calisthenic exercises, and training of the respiratory muscles. Every two weeks, PT phones the patient for an educational reinforcement. |
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Critical Patients Autonomy Planning (CPAP)
Tidsram: Changes from baseline and 4 weeks, and 6 months after home activity
|
CPAP is a measure of dependency.
CPAP was evaluated at three different time-points: at in-hospital admission (baseline), at discharge (patients are followed for the duration of their in-hospital stay, an expected average time of 4 weeks), and after 6 months of physical activity at home.
|
Changes from baseline and 4 weeks, and 6 months after home activity
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Maximum inspiratory pressure (MIP) and maximum expiratory pressure (MEP)
Tidsram: Changes from baseline and 4 weeks (average time), and 6 months after home activity
|
Respiratory Functionality
|
Changes from baseline and 4 weeks (average time), and 6 months after home activity
|
|
MRF 26
Tidsram: Changes between discharge at 4 weeks (average time) and 6 months after home activity
|
Quality of life evaluation.
|
Changes between discharge at 4 weeks (average time) and 6 months after home activity
|
|
Likert Scale
Tidsram: Changes between discharge at 4 weeks (average time) and 6 months after home activity
|
Satisfaction for patient/caregiver
|
Changes between discharge at 4 weeks (average time) and 6 months after home activity
|
|
Mortality
Tidsram: Changes between 3, 6 and 12 months post-discharge
|
Clinical measure
|
Changes between 3, 6 and 12 months post-discharge
|
|
MRC Scale and/or dynamometer
Tidsram: Changes between baseline, discharge at 4 weeks, and 6 months after home activity
|
Rehabilitative measure referring to muscles force
|
Changes between baseline, discharge at 4 weeks, and 6 months after home activity
|
|
6-min walking test
Tidsram: Changes from baseline and discharge at 4 weeks, and 6 months after home activity
|
Rehabilitative measure evaluating the effort tolerance.
|
Changes from baseline and discharge at 4 weeks, and 6 months after home activity
|
|
EuroQol
Tidsram: Changes between discharge at 4 weeks (average time) and 6 months after home activity
|
Quality of life evaluation
|
Changes between discharge at 4 weeks (average time) and 6 months after home activity
|
|
Gussago Nursing Scale
Tidsram: Changes from baseline and 4 weeks, and 6 months after home activity
|
Measure of dependency.
|
Changes from baseline and 4 weeks, and 6 months after home activity
|
|
Barthel Index
Tidsram: Changes from baseline and 4 weeks, and 6 months after home activity
|
Measure of dependency.
|
Changes from baseline and 4 weeks, and 6 months after home activity
|
|
Pre-morbidity life-style (PLS)
Tidsram: Changes from baseline and 4 weeks, and 6 months after home activity
|
Measure of dependency.
|
Changes from baseline and 4 weeks, and 6 months after home activity
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Piero Ceriana, MD, Fondazione Salvatore Maugeri
- Studierektor: Michele Vitacca, MD, Fondazione Salvatore Maugeri
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- UTIR
- Dlg. 5685 on 28 May 2010 (Annat bidrag/finansieringsnummer: Lombardy Region)
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