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Telemedicine Rash Evaluation and Assessment of Toxicity in Skin in Acute Oncology and Haematology Care: A Pilot Study

TREATS: Telemedicine Rash Evaluation and Assessment of Toxicity in Skin in Acute Oncology and Haematology Care: A Pilot Study

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07476807
Acronym
TREATS
Enrollment
25
Registered
2026-03-17
Start date
2026-04-01
Completion date
2026-09-12
Last updated
2026-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rash, Systemic Treatments, Tele-assessment

Brief summary

This study is being done to find out if video consultations (telemedicine) can be used to safely and effectively assess and manage skin problems caused by cancer treatments. Instead of always coming to the hospital for a face-to-face appointment, the patient may be able to use thier smartphone or computer to show your skin to a nurse or doctor over a secure video call. the researchers want to see if this is as good as a regular clinic visit, and whether patients and staff are happy with this new way of working.

Interventions

OTHERtelem healthassessment

SOC is face to face assessment-this study aims to use telemedecine toassess Treatment related skin disorders

Sponsors

Sligo General Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Participants must meet all of the following criteria: * Adult oncology or haematology patients currently receiving systemic anti-cancer therapy (SACT). * New-onset dermatologic toxicity consistent with a recognised adverse effect of the administered SACT. * Skin toxicity severity graded ≤ Grade 2 in accordance with UKONS assessment criteria. * Clinically stable condition not requiring urgent in-person evaluation. * Access to, and ability to use, a smartphone or computer with adequate internet connectivity to participate in telemedicine consultations.

Exclusion criteria

Participants will be excluded if any of the following criteria apply: * Skin toxicity graded ≥ Grade 3 according to UKONS assessment criteria. * Clinical status requiring urgent or immediate face-to-face medical assessment. * Dermatologic toxicity that is atypical, unexpected, or not consistent with known SACT-related adverse effects. * Inability to access or effectively use the required telemedicine technology.

Design outcomes

Primary

MeasureTime frameDescription
time to clinical resolution6 weeksNumber of days from first AHOS contact to documented resolution (Grade 0-1).

Secondary

MeasureTime frameDescription
Escalation in person review6 weeksProportion of telemedicine patients requiring: * Conversion to face-to-face review * Emergency department attendance * Hospital admission
treatment modification reat6 weeksProportion of telemedicine patients requiring: * Conversion to face-to-face review * Emergency department attendance * Hospital admission
unscheduled acute contact6 weeksNumber of unplanned re-contacts with AHOS
Patient-Reported Endpoints -Quality of Life (QoL) and patient satisfaction6 weeksInstrument: QLQ administered: * Post initial assessment * At resolution or week 6

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 29, 2026