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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05936632
Other study ID # 213621
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 24, 2023
Est. completion date December 2023

Study information

Verified date October 2023
Source London School of Economics and Political Science
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To provide timely access to new treatments, some eligible drugs can be approved despite uncertainty surrounding the level of clinical benefit they offer patients. It is not currently known if (and under which circumstances) the public would prefer to wait to access some new drugs in exchange for greater certainty surrounding their clinical benefit. This study aims to elicit the preferences of the US public for wait times and clinical uncertainty of new drugs. To elicit this information, in a survey format, respondents will be presented with a hypothetical scenario and asked to state their preferences for new treatments, each with different attributes.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 850
Est. completion date December 2023
Est. primary completion date December 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Individuals previously or currently diagnosed with any type of cancer. - Individuals with immediate family members previously or currently diagnosed with any type of cancer. Exclusion Criteria: - Individuals without previous or current diagnosis with any type of cancer (themselves or immediate family members).

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Discrete Choice Experiment (DCE)
DCE survey experiment

Locations

Country Name City State
United Kingdom London School of Economics London

Sponsors (1)

Lead Sponsor Collaborator
London School of Economics and Political Science

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Preferences for treatment attributes and trade-offs between attributes. Preferences for different treatment attributes (including clinical uncertainty and wait time), and trade-offs between these, using a study-specific Discrete Choice Experiment (DCE) Questionnaire. Preferences are measured on relative utility scale (arbitrary units, no min/max). Utility indicates preference e.g., higher values are more preferred (better). Through study completion, an average of 4-8 weeks.
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