Home And Locally Observed - Tracking (HALO-Trak)
- Conditions
- Advanced Cancer
- Registration Number
- NCT05971277
- Lead Sponsor
- University College, London
- Brief Summary
The goal of this observational study is to collect biometric, HRQoL, immune response and genomic data continuously and intermittently during and after chemo or immunotherapy for the generation of a complex dataset using a platform which can aggregate different types of data collected over a time period and, to test the potential for analysis within and across data sets with linkage to clinical outcomes. The framework will have capabilities to integrate data from electronic medical records (EMRs) such as Epic, as well as digital streams including sensor, genomic, imaging and pathology. Such a platform can realise the potential for machine learning (ML) methodologies to address important cancer outcomes.
- Detailed Description
The Investigators overarching aim is to determine the relationship between measures of physical performance status including heart rate and steps, health related quality of life (HRQoL) and genomic and immunogenomic phenotype on cancer outcomes in patients receiving chemotherapy or immunotherapy for haematological or metastatic cancer including renal (papillary, and RCC), breast, prostate, and other solid tumours. The primary objective is to test the feasibility of integrating diverse data streams (genomic, HR QoL and biometric) on a novel platform, capable of integrating data streams thus generating complex datasets for analyses using machine learning methodologies.
Secondary objectives will be to conduct exploratory analysis assessing the relationship between individual and combined data types and cancer outcomes.
Analysis using existing and novel computational models will be applied to the data to events in the acute and chronic setting that are common in patients diagnosed with cancer undergoing systemic therapy such as chemotherapy and immunotherapy. The outputs from this study will help inform future studies and trials designed to inform patients about their health status during cancer therapy
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
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● A diagnosis of a metastatic or haematological cancer undergoing systemic therapy
- Undergoing at least 1 planned cycle of chemotherapy or immunotherapy, according to standard of care practices.
- Ability to understand and the willingness to sign a written informed consent.
- Able to ambulate without assistance or walking aid.
- Have an Android or iOS phone and willing to download the Ethera app
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● Physical disabilities that preclude daily walking
- Inability to provide informed consent.
- Unable to use and operate the Ethera Health Monitoring Smartphone App. (Apple or Android)
- Medical or psychiatric condition which in the investigator's opinion would affect the successful completion of the study.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Objective one month to 52 weeks To measure feasibility of data collection longitudinally in a patient cohort undergoing systemic therapy for metastatic or haematological cancer.
Remote monitoring data one month to 52 weeks To collect activity (steps) and heart rate data. This will be collected using the Ethera Wellness app which participants will download onto their smartphone devices.
Clinical Outcome data one month to 52 weeks Data will be collected via an electronic case report form-
Biological sample data. This will include blood samples (30mls) maximum frequency will be monthly one month to 52 weeks This will include blood samples (30mls) and stool samples maximum frequency will be monthly
Quality of life Questionnaire one month to 52 weeks EORTC QLQ C30- questionnaire will be collected monthly
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
UCL London
🇬🇧London, United Kingdom