The effect of physical therapy treatment on the quality of life and physical function of adults hospitalized in the Intensive Care Unit

Effectiveness of a Protocol of Phisiotherapeutical Treatment on Quality of Life and Physical Function of adults Surrender of Intensive Therapy Intervention - Controlled Randomized Clinical Trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

REBEC

Registry ID

RBR-9wghvc

Enrollment

Unknown

Registered

2019-06-28

Start date

2019-05-07

Completion date

Unknown

Last updated

2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscular weakness

Interventions

Individuals with a history of Acute Respiratory Insufficiency and the use of invasive mechanical ventilation in the Intensive Care Unit of both sexes, aged over 18 years up to the age of 59, and who a

Other

G11.427.410.698.277

H02.010.625

Eligibility

Inclusion criteria

Inclusion criteria: Volunteers who meet the following conditions will be eligible for the study: Adults aged 18-59 years; Diagnosed with Acute Respiratory Insufficiency; Inpatient ICU time greater than 7 days; Undergoing mechanical invasive ventilation for more than 48 hours; With the interval from 1 to 30 days after hospital discharge; Clinical stability; (SpO2 greater than 92% in Ambient Air, with Fr less than 35 ipm)

Exclusion criteria

Exclusion criteria: Volunteers who meet the following conditions will be ineligible to participate in the study: Logistic difficulties of transportation for a physical rehabilitation program; Life expectancy less than 6 months; Neurological diseases: Vascular Accident Ischemic and hemorrhagic encephalic, traumatic brain injury. Neurosurgery; Cause of Acute Respiratory Insufficiency associated with exacerbation of chronic cardiac and / or pulmonary pathologies; Functional sequelae limiting ICU hospitalization; History of dementia or cognitive deficit, ex. Parkinson, Alzheimer; Cognitive change acquired in the internal limitation to the evaluation procedures and rehabilitation protocol; Pregnancy.

Design outcomes

Primary

Measure	Time frame
It is expected to find an improvement in the quality of life assessed by the SF-36 scale and the physical function evaluated by the 6-minute walk test;It is expected to find improvement in physical function evaluated by the 6-minute walk test	—

Secondary

Measure	Time frame
It is expected to find improvement in respiratory muscle strength assessed by manovacuometry;It is expected to find improvement of peripheral muscle strength assessed by the dynamometer;It is expected to find improved functionality evaluated by Time Up and go Test, Barthel index and PERME	—

Countries

Brazil

Contacts

Public ContactHospital das Clínicas;Shirley UFPE;Campos

Hospital das Clínicas da Universidade Federal de Pernambuco;Shirley Lima Campos

cephcufpe@gmail.com;shirleylcampos@uol.com.br+558121263743;81- 2126-7383

Outcome results

None listed

Source: REBEC (via WHO ICTRP)