Skip to main content
Clinical Trials/ISRCTN15676570
ISRCTN15676570
Active, not recruiting
未知

A multi-centre, single-arm feasibility study of a complex intervention to improve Recovery after an Episode of Delirium in adults over 65 years: the RecoverED study

Royal Devon University Healthcare NHS Foundation Trust0 sites120 target enrollmentDecember 13, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Delirium
Sponsor
Royal Devon University Healthcare NHS Foundation Trust
Enrollment
120
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

2023 Protocol article in https://pubmed.ncbi.nlm.nih.gov/37715277/ (added 18/09/2023)

Registry
who.int
Start Date
December 13, 2022
End Date
October 31, 2024
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Current participant inclusion criteria as of 01/11/2023:
  • 1\. Aged over 65 years
  • 2\. Admitted to an acute hospital
  • 3\. Clinical diagnosis of delirium while admitted to hospital
  • 4\. Expected to be living in a private dwelling after discharge from hospital or immediate care (a period of 4 weeks of intermediate care will be allowed before discharge home)
  • 5\. Has a carer who could be approached for the study
  • 6\. Has the capacity to provide informed consent to participate, OR, has a consultee who is able to give an opinion on the participation of the person with delirium (in England), OR, has a relative/welfare guardian who is able to give informed consent on behalf of the person with delirium (in Scotland).
  • 7\. Lives within the geographical boundary of the local intervention delivery team
  • 1\. Family member or friend of the person with delirium
  • 2\. In contact with patient participant for at least one hour per week

Exclusion Criteria

  • Current participant exclusion criteria as of 01/11/2023:
  • 1\. Diagnosis of delirium cannot be confirmed during the patient’s hospital visit
  • 2\. Unable to communicate verbally due to advanced dementia or aphasia
  • 3\. Carer declines participation in the study
  • 4\. Undergoing end\-of\-life care
  • 5\. Participating in another intervention study
  • There are no exclusion criteria for carer participants
  • Previous participant exclusion criteria:
  • 1\. Diagnosis of delirium cannot be confirmed during the patient’s hospital visit
  • 2\. Unable to communicate verbally due to advanced dementia or aphasia

Outcomes

Primary Outcomes

Not specified

Similar Trials