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Clinical Trials/ISRCTN99336264
ISRCTN99336264Completed未知

Enhancing recovery of patients admitted to acute settings with hip fracture who are identified as experiencing confusion: a multi-centre, cluster-randomised controlled, feasibility trial of the PERFECTED Enhanced Recovery (PERFECT-ER) care versus standard acute care

niversity of East Anglia0 sites282 target enrollmentStarted: September 5, 2016Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
282

Study Overview

Brief Summary

2017 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/29202786 protocol 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/35228288/ (added 28/10/2022) 2023 Results article in https://pubmed.ncbi.nlm.nih.gov/36737086/ (added 06/02/2023)

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
All

Inclusion Criteria

  • 1. Patient must have had a confirmed proximal hip fracture requiring an operation and be aged 60 or older at time of operation
  • 2. Patient has a pre-op AMTS of 8 or below (including those with 0 because of an inability to answer questions)
  • 3. Patient must have a ‘suitable informant’ (e.g. relative, unpaid or paid carer, care home manager) who has a minimum of once a week face-to-face contact with the patient and is able, and consents to, provide information on proxy measures
  • 4. Patient and a ‘suitable informant’ must be recruited into the trial within 5 days of the hip fracture operation
  • 5. Patient must spend a minimum of 5 days on the study ward

Exclusion Criteria

  • 1. Decision taken not to have hip surgery
  • 2. Patient not expected to survive beyond 4 weeks and therefore it is unlikely that follow-up data will be collected

Investigators

Sponsor
niversity of East Anglia

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