Rehabilitation Following Critical Illness
Primary Purpose
Critical Illness Myopathy
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Pulmonary Rehabilitation
Sponsored by
About this trial
This is an interventional treatment trial for Critical Illness Myopathy focused on measuring critical care, intensive care, weakness, myopathy, paresis, rehabilitation
Eligibility Criteria
Inclusion Criteria:
- Age >18 years AND admitted to critical care unit
- Ventilated >48-hours (via endotracheal tube) OR received continuous non- invasive ventilation (NIV)/non-invasive continuous positive airways pressure (CPAP)
- Admitted to ICU > 48-hours and evidence of SIRS
- Glasgow Coma Score (GCS) 15 (of 15) AND Abbreviated Mini-Mental Test Score (AMMTS) >/= 8 (of 10) on enrolment into rehabilitation programme
- Mobilising on ward to a degree sufficient as to begin a majority of proposed exercises. Clinical stability for observed exercise as judged by trial team is a prerequisite.
- Participant willingness to complete a programme of exercise based therapy aimed at reducing weakness and shortness of breath: subjective weakness or dyspnoea relative to their pre-admission state is implicit
Exclusion Criteria:
- Patients referred for terminal care or prognosis likely to be less than 12-months
- Unstable coronary artery syndrome
- Limb amputation (given special requirement for orthotics/rehabilitation)
- Critical peripheral vascular disease awaiting re-vascularisation procedure (or claudication distance <100 metres)
- Stroke with hemiparesis (likely need for specialised rehabilitation/stay on stroke unit)
- Severe, disabling locomotor problem or severe burns, which prevent effective participation in the exercises contained in the rehabilitation programme.
- Psychiatric disease necessitating anti-psychotic medication, deliberate drug overdose as the admitting ICU indication, ongoing treatment for drug or alcohol addiction, persons of no fixed abode post-discharge
- Patients undergoing renal haemodialysis (given the associated commitment to outpatient attendance)
- Extra contractual ICU referral (only if distance greater than suitable for twice weekly travel)
Additional exclusion criteria for muscle biopsy samples:
- Coagulopathy e.g. warfarin use
Sites / Locations
- St.Thomas' Hospital
- King's College Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control
Intervention
Arm Description
Pulmonary Rehabilitation
Outcomes
Primary Outcome Measures
Incremental Shuttle Walk Test
Secondary Outcome Measures
Health Related Quality of Life
Full Information
NCT ID
NCT00976807
First Posted
September 11, 2009
Last Updated
January 5, 2015
Sponsor
Guy's and St Thomas' NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT00976807
Brief Title
Rehabilitation Following Critical Illness
Official Title
A Randomised Controlled Trial of Rehabilitation Following Critical Illness: A Short Term Feasibility and Follow-Up Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
November 2009 (undefined)
Primary Completion Date
November 2012 (Actual)
Study Completion Date
November 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Guy's and St Thomas' NHS Foundation Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The principal research question to be answered by this study is whether an exercise based rehabilitative intervention following critical illness can generate improvements in exercise capacity and quality of life beyond current (usual) care. The investigators will also aim to demonstrate that such an intervention is both practical and cost-effective.
Detailed Description
Advances in medicine mean that an increasing number of critically ill people, including those with severe pneumonia (lung infection), chronic obstructive pulmonary disease (also known as emphysema or chronic bronchitis) or the "acute respiratory distress syndrome", survive admission to the hospital intensive care unit. Survivors report health problems such as breathlessness and weakness long after discharge. In a study monitoring over 800 patients discharged from an intensive care ward, over half required some form of caregiver assistance after 1-year.
Whilst on intensive care, patients usually require help to breathe from a ventilator machine and become immobilised. This leads to weak breathing muscles in three quarters of patients, as well as weak and wasted arm and leg muscles. Survivors struggle to regain their previous level of daily activity and function, limited by shortness of breath, muscle weakness and tiredness. It is recognised that people with chronic lung problems, such as chronic obstructive pulmonary disease, face similar problems. In this condition, exercise based therapy has been shown to improve muscle strength, walking ability, shortness of breath, and importantly quality of life.
Given these experiences, a new trial will evaluate a novel programme of exercise-based rehabilitation training in patients discharged from intensive care. The programme will last for 8-weeks and will use exercises designed to correct the breathing and limb muscle weakness, as well as education to help patients cope more effectively. The programme will begin as soon as possible following discharge from hospital and will be conducted on a mostly outpatient basis until the course is completed. By speeding the recovery of strength and activity, it is anticipated that quality of life will be improved, which this trial will attempt to measure.
The rehabilitation programme will include aerobic cardiovascular, and upper and lower limb strengthening exercises, in addition to relevant education sessions.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness Myopathy
Keywords
critical care, intensive care, weakness, myopathy, paresis, rehabilitation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Pulmonary Rehabilitation
Intervention Type
Other
Intervention Name(s)
Pulmonary Rehabilitation
Intervention Description
Eight week programme of twice-weekly (sixteen sessions) supervised exercise and education sessions. Exercise will include aerobic cardiovascular and upper and lower limb strengthening exercises. Each session will comprise a warm-up period, followed by individualised exercises, and completed with a cool-down, and last approximately 40minutes.
Aerobic exercise will be prescribed based on the results of walking tests and include walking, step-ups, cycling, and strength prescription according to the repetition maximum principle. Patients will complete three sets using this weight.
Furthermore Borg scores will be used within each session to guide and direct exercise intensity. A home exercise programme will also be designed and accompanied by a manual detailing the individual warm-up, exercises and cool-down, and diary sections to record independent activity.
Each session will also include an education session where relevant.
Primary Outcome Measure Information:
Title
Incremental Shuttle Walk Test
Time Frame
Eight weeks
Secondary Outcome Measure Information:
Title
Health Related Quality of Life
Time Frame
Eight weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age >18 years AND admitted to critical care unit
Ventilated >48-hours (via endotracheal tube) OR received continuous non- invasive ventilation (NIV)/non-invasive continuous positive airways pressure (CPAP)
Admitted to ICU > 48-hours and evidence of SIRS
Glasgow Coma Score (GCS) 15 (of 15) AND Abbreviated Mini-Mental Test Score (AMMTS) >/= 8 (of 10) on enrolment into rehabilitation programme
Mobilising on ward to a degree sufficient as to begin a majority of proposed exercises. Clinical stability for observed exercise as judged by trial team is a prerequisite.
Participant willingness to complete a programme of exercise based therapy aimed at reducing weakness and shortness of breath: subjective weakness or dyspnoea relative to their pre-admission state is implicit
Exclusion Criteria:
Patients referred for terminal care or prognosis likely to be less than 12-months
Unstable coronary artery syndrome
Limb amputation (given special requirement for orthotics/rehabilitation)
Critical peripheral vascular disease awaiting re-vascularisation procedure (or claudication distance <100 metres)
Stroke with hemiparesis (likely need for specialised rehabilitation/stay on stroke unit)
Severe, disabling locomotor problem or severe burns, which prevent effective participation in the exercises contained in the rehabilitation programme.
Psychiatric disease necessitating anti-psychotic medication, deliberate drug overdose as the admitting ICU indication, ongoing treatment for drug or alcohol addiction, persons of no fixed abode post-discharge
Patients undergoing renal haemodialysis (given the associated commitment to outpatient attendance)
Extra contractual ICU referral (only if distance greater than suitable for twice weekly travel)
Additional exclusion criteria for muscle biopsy samples:
Coagulopathy e.g. warfarin use
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicholas Hart, BSc (Hons), MBBS, MRCP, PhD
Organizational Affiliation
St.Thomas' Hospital
Official's Role
Study Director
Facility Information:
Facility Name
St.Thomas' Hospital
City
London
ZIP/Postal Code
SE1 7EH
Country
United Kingdom
Facility Name
King's College Hospital
City
London
ZIP/Postal Code
SE5 9RS
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
25703957
Citation
Connolly B, Thompson A, Douiri A, Moxham J, Hart N. Exercise-based rehabilitation after hospital discharge for survivors of critical illness with intensive care unit-acquired weakness: A pilot feasibility trial. J Crit Care. 2015 Jun;30(3):589-98. doi: 10.1016/j.jcrc.2015.02.002. Epub 2015 Feb 7.
Results Reference
derived
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Rehabilitation Following Critical Illness
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