Topic: Generic Health Relevance and Cross Cutting Themes
Conditions
Interventions
Group 1 (control group) will receive usual physical rehabilitation therapy (Monday to Friday), including a once-daily functional retraining session.
Group 2 (intervention group) will receive a more i
Sponsors
Newcastle upon Tyne Hospitals NHS Foundation Trust (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Participant has provided written informed consent, or their Personal Consultee has provided a signed Personal Consultee Declaration Form, for participation in the study, prior to any study specific procedures taking place 2. Medical and surgical patients (surgical patients are those admitted to ICU as a direct consequence of an operative procedure, or as a consequence of that procedure. All other patients are termed medical) 3. Age 18 years or over 4. Invasive or noninvasive ventilation for more than 48 hours Target Gender: Male & Female ; Lower Age Limit 18 years
Exclusion criteria
Exclusion criteria: 1. Invasive or non-invasive ventilation for more than 72 hours 2. Under 18 years 3. Patients receiving end-of-life care 4. Patients not expected to survive for more than 48 hours after enrolment 5. Acute brain injury 6. Acute spinal cord injury 7. Spinal surgery 8. Brain surgery 9. Multiple trauma 10. Burns 11. Rapidly progressive neuromuscular disease 12. Enrolment in another clinical trial 13. Post-cardiac arrest
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Physical QoL; Timepoint(s): 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Changes in mental health; Timepoint(s): 6 months 2. Economic costs of intervention; Timepoint(s): 6 months | — |
Countries
United Kingdom
Outcome results
None listed