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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05168436
Other study ID # CA209-9W6
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 5, 2019
Est. completion date July 13, 2020

Study information

Verified date December 2021
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this observational study is to determine patients' and professionals' preferences for the characteristics (attributes) of the treatment for Renal cell carcinoma (RCC) in Spain and Portugal.


Description:

This study uses a literature review, qualitative (focus groups) and quantitative methods (discrete-choice experiment, DCE) to determine renal cell carcinoma (RCC) participants and oncologists' preferences. In this clinical trial, the study team will develop a survey consisting of comparisons of hypothetical treatment profiles (scenarios). Scenarios are presented to participants, and each participant chooses the most preferable.


Recruitment information / eligibility

Status Completed
Enrollment 105
Est. completion date July 13, 2020
Est. primary completion date July 13, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: Oncologists from Spain and Portugal will be identified by the promoter and invited to participate in the study in accordance with the inclusion criteria described below. - The oncologist is currently working in a Spanish or Portuguese public hospital. - The oncologist has at least 2 years of experience in the management of participants with Renal Cell Carcinoma (RCC). - The oncologist has agreed to participate in the study. Participants with a diagnosis of RCC will be identified and recruited by the Principal Investigators of the study, taking into account the inclusion criteria described below. - The participant has been diagnosed with RCC for a minimum of 2 months before study inclusion. - The participant has received or is currently receiving pharmacological treatment for RCC; - The participant has provided the informed consent to participate in the study. - The participant must be able to read, understand and complete the survey instrument according to the judgment of the responsible physician. Exclusion Criteria: • Not applicable

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Spain Local Institution Castellon de La Plana

Sponsors (1)

Lead Sponsor Collaborator
Bristol-Myers Squibb

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Utility: Renal cell carcinoma (RCC) participants' preferences Utility (preference score) derived for a treatment alternative choice (scenario) At Baseline
Primary Utility: Oncologists' preferences Utility (preference score) derived for a treatment alternative choice (scenario) At Baseline
Secondary Distribution of socio-demographic characteristics of Renal cell carcinoma (RCC) participants: Age Mean age, defined as the difference in time between date of birth and baseline visit At Baseline
Secondary Distribution of clinical characteristics of RCC participants: Time since RCC diagnosis Mean time to diagnosis, defined as the differences in time between date of diagnosis and baseline visit At Baseline
Secondary Distribution of socio-demographic characteristics of RCC participants: Place of residence Place of residence, defined as Province of residence categories at baseline visit At Baseline
Secondary Distribution of socio-demographic characteristics of RCC participants: Gender Gender, defined as Gender categories at baseline visit, defined as female and male At Baseline
Secondary Distribution of socio-demographic characteristics of RCC participants: Economic status (income) Economic status, defined as Euros per month At Baseline
Secondary Distribution of socio-demographic characteristics of RCC participants: Education level Education level, defined as education level categories at baseline visit, defined as primary education, secondary education, university education, third-level studies (masters, doctorate, etc.) At Baseline
Secondary Distribution of socio-demographic characteristics of RCC participants: Working situation Working situation, defined as working situation categories at baseline visit defined as full-time employed, part-time employed, self-employed, employed but on temporary sick leave due to RCC, permanent sick leave due to RCC, student, unemployed, retired, housework At Baseline
Secondary Distribution of socio-demographic characteristics of RCC participants: Transport to the hospital: means, duration and cost At Baseline
Secondary Distribution of socio-demographic characteristics of RCC participants: Other costs derived from the visit to the hospital (parking, meals...) At Baseline
Secondary Distribution of clinical characteristics of RCC participants: American Joint Committee on Cancer (AJCC) Staging AJCC staging, defined as AJCC disease staging categories at baseline visit defined as Localized disease: Stages I and II; or advanced disease: Stages III and IV At Baseline
Secondary Distribution of clinical characteristics of RCC participants: Charlson index Charlson index, defined as Mean score according to Charlson comorbidity index At Baseline
Secondary Distribution of clinical characteristics of RCC participants: Karnofsky Performance Scale Index Karnofsky Performance Scale Index categories at baseline visit, defined as (0-100%); Lower score representing worst functional impairment At Baseline
Secondary Distribution of clinical characteristics of RCC participants: Current drug treatment (if applicable) Current drug treatment, defined as drug treatment categories at baseline visit At Baseline
Secondary Distribution of clinical characteristics of RCC participants: Identification of previous pharmacological treatments received by the participant for the treatment of RCC Previous drug treatment, defined as drug treatment categories at baseline visit At Baseline
Secondary Distribution of clinical characteristics of RCC participants: Description of previous pharmacological treatments received by the participant for the treatment of RCC Previous drug treatment, defined as drug treatment categories at baseline visit At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Gender Gender, defined as Gender categories at baseline visit, defined as female and male At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Age Mean age, defined as the difference in time between date of birth and baseline visit At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Province where employed Province where employed, defined as Province categories at baseline visit At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Years of experience in RCC Years of experience in RCC, defined as Mean time of experience in RCC at baseline visit At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Years of experience in oncology Years of experience in oncology, defined as Mean time of experience in oncology at baseline visit At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Number of participants with RCC seen per year Number of participants with RCC seen per year, defined as Mean time of participants with RCC seen per year At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Other types of cancer treated Other types of cancer treated, defined as other cancers treated At Baseline
Secondary Distribution of socio-demographic characteristics of oncologists: Level/ classification of hospital where employed Hospital level or classification categories at baseline visit, defined as first, second, third, and fourth level At Baseline
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