ClinicalTrials.gg
Enrolling by invitationNCT07476807TREATSUpdated Apr 28, 2026

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

An interventional study of telem healthassessment in Rash, Systemic Treatments and Tele-assessment, sponsored by Sligo General Hospital. Enrolling by invitation at 1 site in Ireland. Per ClinicalTrials.gov, last updated 2026-04-28.

Sponsored by Sligo General Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
25
Allocation
Not applicable
Sex
All
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Study 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.

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Conditions studied

  • Rash
  • Systemic Treatments
  • Tele-assessment

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In context

Exanthema

68 studies on the registry are indexed under Exanthema; 11 are open to participants now.

This study's planned enrollment of 25 is below the median of 60 across 45 interventional studies indexed under Exanthema.

Browse Exanthema studies →

Lead sponsor

Sligo General Hospital is the lead sponsor of 5 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

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.
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
25 participants (estimated)

Study arms

  • Other
    Remote tele medicine assessment

    use of telemedicine

    Other: telem healthassessment

Interventions

  • Othertelem healthassessment

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

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What researchers measure

Primary outcomes

  1. time to clinical resolution

    Number of days from first AHOS contact to documented resolution (Grade 0-1).

    Time frame: 6 weeks

Secondary outcomes

  1. Escalation in person review

    Proportion of telemedicine patients requiring: * Conversion to face-to-face review * Emergency department attendance * Hospital admission

    Time frame: 6 weeks

  2. treatment modification reat

    Proportion of telemedicine patients requiring: * Conversion to face-to-face review * Emergency department attendance * Hospital admission

    Time frame: 6 weeks

  3. unscheduled acute contact

    Number of unplanned re-contacts with AHOS

    Time frame: 6 weeks

  4. Patient-Reported Endpoints -Quality of Life (QoL) and patient satisfaction

    Instrument: QLQ administered: * Post initial assessment * At resolution or week 6

    Time frame: 6 weeks

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Study locations

1 site
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References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07476807
Lead sponsor
Sligo General Hospital
Responsible party
Margaret Burke (Research Nurse, Sligo General Hospital) — Principal investigator
First posted
Mar 17, 2026
Start date
Apr 1, 2026
Primary completion
Apr 1, 2026
Completion
Sep 12, 2026 (estimated)
Last update
Apr 28, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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