PERFECTED CRCT: Care of patients experiencing hip fracture & confusio

Not Applicable

Completed

• Conditions: Specialty: Ageing, Primary sub-specialty: Ageing; UKCRC code/ Disease: Neurological/ Other degenerative diseases of the nervous system; Mental and Behavioural Disorders; Confusion

• Registration Number: ISRCTN99336264
• Lead Sponsor: niversity of East Anglia

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)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-09-05
• Study Completion: 2018-07-31
• Last Update Posted: 20 February 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 282

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> Feasibility outcomes:<br> 1. Recruitment rate<br> 2. Retention rate<br>

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration