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Clinical Trials/NCT05044221
NCT05044221
Unknown
N/A

Supporting the Recovery Needs of Patients Following Intensive Care

University of Melbourne2 sites in 1 country40 target enrollmentAugust 31, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Post Intensive Care Unit Syndrome
Sponsor
University of Melbourne
Enrollment
40
Locations
2
Primary Endpoint
Lived experiences and opinions
Last Updated
4 years ago

Overview

Brief Summary

Recovery for intensive care survivors is limited by ongoing problems with walking, strength, fatigue, mental distress and cognitive morbidity known as 'Post Intensive Care Syndrome'. There has been increasing interest in ways that clinicians can support patients in their post ICU recovery.

The investigators are undertaking a co design approach to informing the design of a recovery pathway for patients who have been admitted to the intensive care to support them in their return to home, family and working responsibilities.

Detailed Description

This project will aim to involve \~ 20 past ICU patient/family members and \~20 health professionals to participate in a co-design approach to examine the recovery needs and resources that are required to support patients after leaving hospital. Using an experience based co design methodology three 2-hour workshops will be run with the first workshop involving patients/family members, the second involving healthcare professionals to separately gain thoughts and perspectives, and then the final workshop which will be combined to identify and problem solve priority resources and solutions.

Registry
clinicaltrials.gov
Start Date
August 31, 2021
End Date
July 2022
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Selina M Parry

Cardiorespiratory Team Lead, Department of Physiotherapy

University of Melbourne

Eligibility Criteria

Inclusion Criteria

  • Hospitalized adults, aged 18 years or over
  • Admitted to the ICU requiring invasive mechanical ventilation for \> 48 hours and remain in the ICU for a minimum of four days
  • Living at home before the current admission (not in a facility and/or no fixed abode)

Exclusion Criteria

  • Non-English speaking (insufficient English language skills to read and understand questionnaires and patient information consent form)
  • Pre-existing documented cognitive impairment
  • Spinal cord injury or other primary neuromuscular disease
  • New lower limb fracture with altered weight bearing status
  • Expected survival \< 3 months according to the treating medical team
  • Active substance abuse or psychosis
  • Lack of access to telephone / computer or inability to use these resources independently (which would impact on ability to complete the intervention)
  • Pregnancy
  • Suicidality
  • Incarcerated

Outcomes

Primary Outcomes

Lived experiences and opinions

Time Frame: 3 months

Capability Opportunity Motivation Barriers and Theoretical Domains Framework will be used to interpret qualitative data from the workshops and interviews.

Study Sites (2)

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