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Recruiting NCT04983199

NCT04983199 Patient Reported Outcomes/Metrics Program Trial

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Clinical Trial Summary
NCT ID NCT04983199
Status Recruiting
Phase
Sponsor University Health Network, Toronto
Condition Metastatic Cancer
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2022-11-24
Primary Completion 2027-09

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Hexoskin Medical System

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2022-11-24 with a primary completion date of 2027-09.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is an observational study to investigate if it is feasible to recruit 100 patients receiving radiotherapy (RT) to metastatic disease to wear Hexoskin and if Hexoskin will facilitate the monitoring, detection and early treatment of RT-related side effects.

Eligibility Criteria

Inclusion Criteria: * Planned to receive palliative radiotherapy for pain * Known cancer diagnosis * Able to wear Hexoskin Medical Shirt * Ability to use and populate the mobile app (Zamplo) with or without assistance * ECOG: 0-3 * Willing to provide a list of analgesic (pain relief) medication * Willing to complete questionnaires * Life expectancy of at least 3 months Exclusion Criteria: * Receiving whole brain radiotherapy * Major cognitive or psychiatric impairments * Pregnant women * Allergies to: polyester, synthetic fibers * Patients with pacemakers or implantable cardioverter-defibrillator (ICD) * Patients on a Holter Monitor

Contact & Investigator

Central Contact

Philip Wong

✉ philip.wong@rmp.uhn.ca

📞 416-946-4501

Principal Investigator

Philip Wong

PRINCIPAL INVESTIGATOR

The Princess Margaret Cancer Foundation

Frequently Asked Questions

Who can join the NCT04983199 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Metastatic Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT04983199 currently recruiting?

Yes, NCT04983199 is actively recruiting participants. Contact the research team at philip.wong@rmp.uhn.ca for enrollment information.

Where is the NCT04983199 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT04983199 clinical trial?

NCT04983199 is sponsored by University Health Network, Toronto. The principal investigator is Philip Wong at The Princess Margaret Cancer Foundation. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology