Skip to content

The RECOVER Study: Rehabilitation after Intensive Care

Evaluation of a Rehabilitation Complex Intervention for patients following Intensive Care Discharge. The RECOVER Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN09412438
Enrollment
240
Registered
2010-09-27
Start date
2010-10-01
Completion date
Unknown
Last updated
2019-05-27

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

Conditions

Rehabilitation

Interventions

Participants will be randomised into one of two groups: Intervention group Standard ward-based care delivered by the NHS service with additional access to enhanced reh

Sponsors

Lothian University Hospitals Division (UK)
Lead Sponsor
University of Edinburgh
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The patient has required 48 hours or more mechanical ventilation in the intensive care unit (ICU) 2. The consultant in charge of the patient considers them fit for discharge from the ICU

Exclusion criteria

Exclusion criteria: Current exclusion criteria as of 07/09/2012: 1. Primary neurological admission diagnosis (brain trauma; intracerebral bleed; stroke; Guillain-Barre syndrome) 2. The clinician in charge of care has agreed with the patient and/or family that only palliative care will be provided. 3. Patients currently receiving home ventilation or planning to commence a program of home ventilation 4. The patient is expected to be discharged from ICU to a non-study hospital where the intervention cannot be received 5. Gaining informed consent, following the intervention or follow-up is not feasible, despite resources available, due to communication difficulties 6. Patient currently enrolled in another RCT with similar endpoints 7. Patient aged <18 years at time of screening Previous exclusion criteria until 07/09/2012: 1. Primary neurological admission diagnosis (brain trauma; intracerebral bleed; stroke; Guillain-Barre syndrome) 2. Patients for whom a dedicated rehabilitation programme already exists (transplantation, stroke) 3. Patient currently enrolled in another RCT with similar endpoints

Design outcomes

Primary

MeasureTime frame
Rivermead Mobility Index, assessed at 3 months

Secondary

MeasureTime frame
The impact of the complex intervention on physical, psychological and social functioning will be measured at 3 months using: 1. Total, Physical Component Score, and Mental Component Score SF12v2 2. Euroqol EQ-5D score 3. Hospital Anxiety and Depression (HAD) questionnaire 4. Davidson's Trauma Scale score (DTS) 5. Nutritional Status (subjective global assessment of nutrition; SGA nutrition) 6. MRC Muscle Strength 7. Hand grip strength strength (HG dynamometry) 8. 2m timed up and go time 9. Visual analogue score 10. Health economic questionnaire 11. Process measures 12. Research Log of Generic Rehabilitation Assistants Assessments at 6 and 12 months - Rivermead Mobility Index, SF12v2, EQ-5D, HAD, DTS and health economic questionnaires, visual analogue score and overall patient satisfaction measure. Additional outcomes: 13. To compare patient and carer experiences between usual care and the new strategy 14. To evaluate the cost-effectiveness of the novel approach

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 26, 2026