NCT07731425

Brief Summary

This study of current or former cancer patients will evaluate whether communicating data on overall survival data in addition to information on progression-free improves the accuracy of cancer patients' expectations about the survival benefits of new cancer drugs

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
3,000

participants targeted

Target at P75+ for not_applicable cancer

Timeline
2mo left

Started Aug 2026

Shorter than P25 for not_applicable cancer

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress1%
Aug 2026Oct 2026

First Submitted

Initial submission to the registry

July 23, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 28, 2026

Completed
4 days until next milestone

Study Start

First participant enrolled

August 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Last Updated

July 28, 2026

Status Verified

July 1, 2026

Enrollment Period

2 months

First QC Date

July 23, 2026

Last Update Submit

July 23, 2026

Conditions

Keywords

cancerprescription drugsprogression-free survival

Outcome Measures

Primary Outcomes (1)

  • Accuracy of expectations about the survival benefits of a new cancer drug approved based on progression-free survival

    Compared to standard treatment, do patients with advanced kidney cancer live longer when treated with Velotrex? \- Response options: definitely yes, probably yes, probably no, definitely no

    Assessed immediately after the intervention

Secondary Outcomes (1)

  • Perceptions of drug benefits and risks

    Assessed immediately after the intervention

Study Arms (6)

FDA explanation for progression-free survival (control)

PLACEBO COMPARATOR
Other: FDA explanation for progression-free survival (control)

FDA explanation for progression-free survival with overall survival data

EXPERIMENTAL
Other: FDA explanation for progression-free survival with overall survival data

NCI explanation for progression-free survival

EXPERIMENTAL
Other: NCI explanation for progression-free survival

NCI explanation for progression-free survival with overall survival data

EXPERIMENTAL
Other: NCI explanation for progression-free survival with overall survival data

Plain-language explanation of progression-free survival

EXPERIMENTAL
Other: Plain-language explanation of progression-free survival

Plain-language explanation of progression-free survival with overall survival data

EXPERIMENTAL
Other: Plain-language explanation of progression-free survival with overall survival data

Interventions

Progression-free survival

FDA explanation for progression-free survival (control)

The description, 'progression-free survival', along with data on overall survival.

FDA explanation for progression-free survival with overall survival data

The description, 'the length of time during and after treatment that a patient lived with the cancer but it did not get worse'.

NCI explanation for progression-free survival

The description, 'the length of time during and after treatment that a patient lived with the cancer but it did not get worse', along with data on overall survival.

NCI explanation for progression-free survival with overall survival data

The description, 'the length of time until a test showed the cancer grew, spread, or worsened'.

Plain-language explanation of progression-free survival

The description, 'the length of time until a test showed the cancer grew, spread, or worsened', along with data on overall survival.

Plain-language explanation of progression-free survival with overall survival data

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • US adults with a current or former cancer diagnosis (excluding nonmelanoma skin cancer)
  • US adults 18 years of age and older, fluent in English, and residing in the United States.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Harvard Medical School and Harvard Pilgrim Health Care Institute

Boston, Massachusetts, 02215, United States

Location

MeSH Terms

Conditions

Neoplasms

Interventions

Progression-Free Survival

Intervention Hierarchy (Ancestors)

Treatment OutcomePrognosisDiagnosisSurvival AnalysisStatistics as TopicEpidemiologic MethodsInvestigative TechniquesOutcome Assessment, Health CareOutcome and Process Assessment, Health CareQuality of Health CareHealth Services AdministrationHealth Care Evaluation MechanismsHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Fellow

Study Record Dates

First Submitted

July 23, 2026

First Posted

July 28, 2026

Study Start

August 1, 2026

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

October 1, 2026

Last Updated

July 28, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Locations