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Clinical Trials/ISRCTN11853373
ISRCTN11853373
Completed
未知

A randomised controlled trial examining the effect of a six week supervised exercise programme on patient fitness and hospital related anxiety and depression following an intensive care length of stay of greater than 48 hours

Abertawe Bro Morgannwg University (ABMU) Health Board (UK)0 sites60 target enrollmentFebruary 7, 2012

Overview

Phase
未知
Intervention
Not specified
Conditions
Any patient who has been a patient on ICU (general) for 48 hours or more
Sponsor
Abertawe Bro Morgannwg University (ABMU) Health Board (UK)
Enrollment
60
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/30792758 (added 12/06/2019)

Registry
who.int
Start Date
February 7, 2012
End Date
August 30, 2017
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Abertawe Bro Morgannwg University (ABMU) Health Board (UK)

Eligibility Criteria

Inclusion Criteria

  • 1\. Male or female patients who are aged 18 years or more (no upper age limit)
  • 2\. Patients who have had a length of stay on ICU for more than 48 hours
  • 3\. Patients who have been discharged home and are attending follow up clinic within 6 months of their discharge from ICU
  • 4\. Patients who can follow instructions
  • 5\. Patients who are not already enrolled in a rehabilitation programme
  • 6\. Patients who live within commutable distance

Exclusion Criteria

  • 1\. Patients who do not consent to participation in the study
  • 2\. Patients aged less than 18 years
  • 3\. Patients hospitalised for longer than 6 months since their discharge from ICU
  • 4\. Patients who lack capacity to follow instructions
  • 5\. Patients who are already enrolled in a rehabilitation programme
  • 6\. Patients who live outside of commutable distance
  • 7\. Patients with any medical contraindications to exercise, including:
  • 7\.1\. Unstable angina or myocardial infarction in the preceding month
  • 7\.2\. Unmanaged valvular problems
  • 7\.3\. Patients awaiting further definitive treatment (e.g. open abdominal wound)

Outcomes

Primary Outcomes

Not specified

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