Home And Locally Observed - Tracking (HALO-Trak)

Sponsor
University College, London (Other)
Overall Status
Recruiting
CT.gov ID
NCT05971277
Collaborator
(none)
200
1
38
5.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Device: Halo Wearable data device

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

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Proof of Concept (POC) Prospective Observational Study to Test a Framework for Integration of Data Streams, Including Molecular Genomic Markers and Wearable Device Data in Patients Receiving Chemotherapy for Advanced Cancer
Actual Study Start Date :
Jan 30, 2023
Anticipated Primary Completion Date :
Apr 1, 2025
Anticipated Study Completion Date :
Apr 1, 2026

Outcome Measures

Primary Outcome Measures

  1. 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.

  2. 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.

  3. 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

  4. Clinical Outcome data [one month to 52 weeks]

    Data will be collected via an electronic case report form-

  5. Quality of life Questionnaire [one month to 52 weeks]

    EORTC QLQ C30- questionnaire will be collected monthly

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • ● 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

Exclusion Criteria:
  • ● 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCL London London United Kingdom W1W 7TY

Sponsors and Collaborators

  • University College, London

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University College, London
ClinicalTrials.gov Identifier:
NCT05971277
Other Study ID Numbers:
  • 150745
  • 312296
First Posted:
Aug 2, 2023
Last Update Posted:
Aug 2, 2023
Last Verified:
Jan 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2023