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HOme USability Evaluation

HOme USability Evaluation

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06134245
Acronym
HOUSE
Enrollment
0
Registered
2023-11-18
Start date
2024-03-01
Completion date
2024-06-30
Last updated
2026-09-11

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

Conditions

Cancer

Brief summary

To validate the usability and safety of the Liberty Analyser.

Interventions

Home monitoring

Sponsors

Entia Ltd
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Undergoing systemic anti-cancer therapy (SACT) * Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0, 1, 2 at enrolment * Adequate English language skills (not requiring a translator) to participate in participant training and use the Entia Liberty analyser * Patients capable of providing written informed consent

Exclusion criteria

* History or current diagnosis of haematological malignancy * Patients with eyesight or hearing limitations or other disabilities that preclude the use of the Entia Liberty analyser or participation in training * Inadequate use and understanding of the English language, requiring a translator

Design outcomes

Primary

MeasureTime frameDescription
The Entia Liberty Analyser is easy to useThrough study completion, 1 dayUsers can easily carry out a test using the Entia Liberty Analyser
The Entia Liberty Analyser is safe to useThrough study completion, 1 dayResults obtained using the Entia Liberty Analyser are valid and reliable

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 12, 2026