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A Study of Adjuvant Melanoma Stakeholder Treatment Preferences

Adjuvant Melanoma Stakeholder Treatment Preference Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05115006
Enrollment
294
Registered
2021-11-10
Start date
2021-01-07
Completion date
2022-06-02
Last updated
2022-06-30

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

Conditions

Melanoma

Keywords

Melanoma, Discrete choice experiment, Resected melanoma, Adjuvant treatment, Patient preference

Brief summary

The purpose of this study is to understand the trade-offs that participants with surgically treated melanoma would be willing to make among key features and outcomes of adjuvant anti-cancer treatments or no adjuvant treatment / observation.

Interventions

None listed

Sponsors

Bristol-Myers Squibb
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Self-reported medical diagnosis of stage II or stage III melanoma * Have been resected (had surgery) for their melanoma within 12 months prior to study participation

Exclusion criteria

* Self-reported stage IIa * Self-reported recurrence of melanoma after surgery Other protocol-defined inclusion/

Design outcomes

Primary

MeasureTime frame
Preference weights or utilities (a measure of relative preference; on a continuous variable scale) for each treatment attribute level based on responses to the Discrete Choice Experiment (DCE) choice tasksAt Baseline

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026