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Clinical Trials/ISRCTN25032672
ISRCTN25032672
Completed
N/A

Rehabilitation enablement in chronic heart failure: a feasibility study

Royal Cornwall Hospitals NHS Trust (UK)0 sites24 target enrollmentMarch 13, 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
Topic: Primary Care Research Network for England, Cardiovascular
Sponsor
Royal Cornwall Hospitals NHS Trust (UK)
Enrollment
24
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

2016 results in https://www.ncbi.nlm.nih.gov/pubmed/27965855 2020 process evaluation in https://pubmed.ncbi.nlm.nih.gov/31377692/ (added 21/08/2020)

Registry
who.int
Start Date
March 13, 2014
End Date
October 4, 2014
Last Updated
5 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Royal Cornwall Hospitals NHS Trust (UK)

Eligibility Criteria

Inclusion Criteria

  • 1\. Adults (aged \=18 years)
  • 2\. Patients who have a confirmed diagnosis of systolic HF on echocardiography (i.e. left ventricular ejection fraction \<45%) within the last 5 years.
  • 3\. Patients who have been clinically stable for at least 2 weeks and in receipt of medical treatment for HF.
  • 4\. Patients deemed suitable for exercise, and who do not have a contraindication to exercise, as adjudged by the site Principal Investigator in collaboration with the local clinical team (with reference to the Amercian Heart Association 2013 guidelines).
  • 5\. Provision of informed consent to participate.
  • Patient's caregivers aged 18 years or older may participate if the meet the following definition: ?Someone who provides unpaid support to a family member or friend with heart failure who is enrolled in the study'.
  • Intervention nurses will only participate following completion of the HF Manual training course and the provision of informed consent to provide study data.

Exclusion Criteria

  • 1\. Patients who have undertaken cardiac rehabilitation (CR) within the last 12 months
  • 2\. Patients who have received an ICD or CRT or combined CRT/ICD device implanted in the last 6 months.
  • 3\. Patients who are in a long\-term care establishment or who are unwilling or unable to travel to research assessments or accommodate home visits.
  • 4\. Patients who are unable to read English.
  • 5\. Patients judged to be unable to participate in the study for any other reason e.g. psychiatric disorder, diagnosis of dementia, life threatening co\-morbidity

Outcomes

Primary Outcomes

Not specified

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