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Completed

NCT Number: NCT02415634

REhabilitation After Critical Illness Assisted Discharge Pack (RECAP)

The complexity of critical illness can result in both physical and psychological consequences for survivors, which can extend past the intensive unit care stay and after hospital discharge. A need for information and empowerment in the recovery process are highlighted for developing treatment strategies. It is suggested that there is a relationship between physical problems and psychological symptoms, but this has not been researched. This pilot study aims to test the effectiveness of a physiotherapy directed Rehabilitation after Critical illness Assisted discharge Pack (RECAP) on the physical and psychological function of patients recovering from critical illness in the first three weeks post discharge from ICU to the general ward area. The study will rely on a randomized controlled clinical trial design, with patients assigned to either a "usual care" control group vs. the treatment group. It is expected that engaging patients in their rehabilitation plan will focus physiotherapy treatment and improve physical recovery. It is hypothesized that the RECAP will reassure, support and empower patients to directly affect their psychological recovery in the first three weeks after critical illness.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St. Vincent's University Hospital

Dublin, Ireland

About this study

The process of recovering from critical illness is complex. The physical and psychological consequences of surviving critical illness can extend past the intensive unit care stay and after hospital discharge. For a critically ill patient, their first transition is being discharged from intensive care to a general ward and is one of the most stressful transitions they experience. They are required to adjust both physically and psychologically as they begin an uncertain journey to recovery. Research on the patient experience has identified vulnerability, hopelessness, fear of the unknown and anxiety as key features of this transition. A need for information and empowerment in the recovery process are highlighted for developing treatment strategies. It is suggested that there is a relationship between physical problems and psychological symptoms but this has not been researched. There is also limited evidence to guide clinicians in treatment strategy choice for these patients. This pilot study aims to test the effectiveness of a physiotherapy directed Rehabilitation after Critical illness Assisted discharge Pack (RECAP) on the physical and psychological function of patients recovering from critical illness in the first three weeks post discharge from the ICU to the general ward area. The study will rely on a randomized controlled clinical trial design, with patients assigned to either a "usual care" control group vs. the treatment group. Individuals in the treatment group will receive "usual care" plus a RECAP pack at ICU discharge with once weekly follow up with an ICU physiotherapist. The intervention group will receive the RECAP plus standard physiotherapy for the first three weeks after intensive care stay and the control group will receive standard physiotherapy alone. Outcome measures used will be the Functional Independence Measure (FIM) and State Anxiety Inventory (SAI). Secondary Outcome measures will include the Chelsea Critical Care Physical Assessment Tool (CPAx) and a 5 question patient satisfaction questionnaire. Outcome measures will be taken at ICU discharge, at one week post ICU discharge and at three weeks after ICU discharge to determine physical and psychological recovery, along with evaluating overall study feasibility. It is expected that engaging patients in their rehabilitation plan will focus physiotherapy treatment and improve physical recovery. It is hypothesized that the RECAP will reassure, support and empower patients to directly affect their psychological recovery in the first three weeks after critical illness.

The User Centred Critical Care Discharge Information Pack (UCCDIP) and instructions, designed by Bench and Day (2012), will be used as a component of the RECAP. These are being used with the authors permission.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients admitted to ICU >4 days
  • Indication for physiotherapy referral in ICU
  • Indication for follow up physiotherapy on discharge from the ICU
  • Age>18 years
  • RASS score 0 at time of consent

Exclusion criteria

  • ICU length of stay >14 days
  • Patients with a multi-disciplinary team based work-up in advance of a planned ICU admission (e.g. Liver transplant)
  • Pregnant mothers
  • Palliation
  • Expected discharge to another hospital
  • Unable to understand English
  • Patients who have direct access to condition specific MDT follow up (e.g. Stroke, Neurology)
  • Psychiatric Disease
  • Unstable Cardiac Disease
  • Where physiotherapy treatment is limited or maximal functional capacity is capped for duration of study (e.g. Non Weight Bearing status due to orthopaedic limitation x 12 weeks.
  • Patients who are unable to give consent

Treatment and study plan

RECAP

Other

Patients will receive an information pack at ICU discharge called the RECAP. This pack will include

  • Part 1: A critical care discharge summary (UCCDIP) (Bench and Day, 2012)
  • Part 2: A rehabilitation goal setting care plan
  • Part 3: A patient communication forum
  • Part 4: Useful supports and contact information
  • Part 5: Tailored exercise programme

The patient will have a consultation with the ICU physiotherapist before ICU discharge once weekly thereafter for 3 weeks . The focus of the session will be to discuss goal attainment and associated challenges.

The ICU therapist will meet once weekly with the patient's primary physiotherapist to provide clinical support if necessary, in determining the patient's needs post critical care.

Control

Other

Participants allocated to the control group will receive standard physiotherapy intervention post ICU discharge

Primary outcomes

  1. Change from baseline in Functional Independence Measure (FIM)

    Time frame: Assessed at week three to detect change from baseline FIM score as a result of intervention

    A measure of physical and cognitive function

  2. Change from baseline State Anxiety inventory (SAI), a subscale of State-Trait Anxiety Inventory

    Time frame: Assessed at week one to detect change from baseline in SAI score as a result of intervention

    A measure of state anxiety

  3. Change from baseline State Anxiety inventory (SAI), a subscale of State-Trait Anxiety Inventory

    Time frame: Assessed at week three to detect change from baseline in SAI score as a result of intervention

    A measure of state anxiety

Secondary outcomes

  1. Chelsea Critical Care Physical Assessment Tool (CPAx)

    Time frame: Assessed at day one

    Measure of physical function

  2. Patient Rehabilitation Satisfaction Questionnaire

    Time frame: 3 weeks post intensive care discharge

    a measure of patient satisfaction with rehabilitation experience

Sponsors and collaborators

Lead sponsor

Maire Gilmartin

Other

Collaborators

  • St Vincent's University Hospital, Ireland
  • University of Ulster

Registry information

Official study title

Investigation of Physiotherapy Led ICU Discharge Facilitation Using the REhabilitation After Critical Illness Assisted Discharge Pack (RECAP) Model; a Pilot Randomized Controlled Trial.

Acronym: RECAP

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Apr 14, 2015
Registry last updated
Nov 17, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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