MedPath

The role of an automated frailty score (electronic frailty index) in improving outcomes for cancer patients in chemotherapy

Not Applicable
Completed
Conditions
Cancer
Malignant neoplasm
Registration Number
ISRCTN28080501
Lead Sponsor
Royal Surrey County Hospital NHS Foundation Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
25
Inclusion Criteria

1. Stakeholders (n=10)
1.1. 5 Medical and Clinical Oncologists, General Practitioners, Geriatricians
1.2. 5 Chemotherapy and Specialist Nurses
2. Patients (n=10)
2.1. 2 patients aged 60 - 70 with newly diagnosed stage II or III breast cancer and 2 >70 years old
2.2. 3 patients with stage 3 colon cancer (1 60 - 70 years old and 2 >70 years old)
2.3. 3 patients with Stage IIIB-IV non-small cell lung cancer (1 - 60-70 years old and 2 >70 years old)
3. Carers (n=5) Purposely selected for gender (men =3, women =2) and relationship to the patient (partner =3 or child =2)

Exclusion Criteria

1. Stakeholders, patients or carers who do not fulfil the criteria described above
2. Are unable to participate in an interview
3. Do not speak/understand English

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Work-package 1:<br>30 day chemotherapy mortality and hospital admissions during chemotherapy.<br>Information will be taken from historical systemic chemotherapy dataset (SACT) records 2013 - 2016 of patients with breast, lung and colorectal cancer. The data will be obtained from the following databases: The Clinical Practice Research Datalink (CPRD), ResearchOne database and Royal College of GPs (RCGP) Research and Surveillance Centre.
Secondary Outcome Measures
NameTimeMethod
Work-package 2: <br>1. The acceptability of eFI (electronic frailty index) will be measured using interview data collected at a single time point that will be analysed with Framework Analysis<br>2. The suitability of the endpoints for a future definitive study - this will be decided once the data from WP1 shows the link between eFI and risk of dying from chemotherapy and risk of admission during chemotherapy. If eFI has a predictive power (the poorer the eFI score the higher the chance of complications) this will be deemed as a suitable endpoint for a future trial<br>3. The overall accuracy between hospital derived eFI and GP-medical records derived eFIGP-eFI) - the eFI and GP-eFI will be directly compared to assess the difference in score<br>4. The ease of access to GP-eFI and HES eFI - this will be a descriptive analysis of the time it takes to extract data and obtain relevant agreements
© Copyright 2025. All Rights Reserved by MedPath