NCT06545188

Brief Summary

The goal of this clinical trial is to learn if mortality salience has an impact on treatment decisions in urologists and patients with urological cancer. The main questions it aims to answer are: Does mortality salience lead to more aggressive treatment decisions in a) urologists and b) patients with urological cancer? Which factors predict more aggressive treatment decisions a) in urologists and b) in patients with urological cancer? Is the Fear of cancer recurrence-1 (FCR-1) in German language a valid screening tool for fear of cancer progression in patients with urological cancer? Researchers will compare a mortality salience trigger to control questions to see if mortality salience leads to more aggressive treatment decisions. Participants will: Answer the Mortality Attitudes Personality survey (MAPS) to trigger mortality salience and, in three borderline case vignettes, provide information on how likely they would be to choose a more aggressive therapy.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
746

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2024

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 15, 2024

Completed
25 days until next milestone

First Posted

Study publicly available on registry

August 9, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

September 16, 2024

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 8, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 8, 2025

Completed
Last Updated

November 24, 2025

Status Verified

February 1, 2025

Enrollment Period

1.1 years

First QC Date

July 15, 2024

Last Update Submit

November 21, 2025

Conditions

Keywords

urological cancermortality saliencefear of deathpsycho-oncologydecision makingdeath anxiety

Outcome Measures

Primary Outcomes (1)

  • treatment decision

    Question about how likely the subject would opt for the more aggressive of two possible therapies on a Likert scale from 0 = very unlikely to 10 = very likely.

    Day 0

Secondary Outcomes (16)

  • Operationalised Psychodynamic Diagnosis (OPD) structure questionnaire, OPD-SQ (Ehrenthal et al., 2015)

    Day 0

  • Relationships-Revised Questionnaire, ECR-RD8 (Ehrenthal et al., 2021)

    Day 0

  • Meaning in Life Questionnaire, MLQ (Steger et al., 2006)

    Day 0

  • Peace of Mind Scale, POMS (Lee et al., 2013)

    Day 0

  • Death Attitude Profile - Revised, DAP-GR

    Day 0

  • +11 more secondary outcomes

Study Arms (2)

Mortality salience trigger

EXPERIMENTAL

Mortality Attitudes Personality Survey (MAPS, Rosenblatt et al. 1998) will be administered (two open questions about death and mortality)

Other: Mortality Attitudes Personality Survey

Dental pain questions (control condition)

OTHER

Two open questions about a dental treatment will be administered

Other: Dental treatment questions (control condition)

Interventions

Two open questions about death and mortality will bei administered to trigger mortality salience

Mortality salience trigger

Two open questions about a dental treatment (control condition)

Dental pain questions (control condition)

Eligibility Criteria

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

You may qualify if:

  • sufficient cognitive ability
  • German language skills

You may not qualify if:

  • none
  • Study 2) Patients
  • urological cancer (ICD-10: C60, C61, C62, C63, C64, C65, C66, C67, C68)
  • age at least 18 years
  • German language skills
  • sufficient cognitive ability
  • capacity to consent
  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Hospital Düsseldorf, Department of Urology

Düsseldorf, 40225, Germany

Location

MeSH Terms

Conditions

Urologic NeoplasmsNecrophobia

Condition Hierarchy (Ancestors)

Urogenital NeoplasmsNeoplasms by SiteNeoplasmsFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesUrologic Diseases

Study Officials

  • Dominik Fugmann, Dr. med.

    Heinrich Heine University Duesseldorf, Germany

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Study 1) Urologists: RCT; two arms - Intervention group \& control group Study 2) Patients with urological cancer: RCT; two arms - Intervention group \& control group
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 15, 2024

First Posted

August 9, 2024

Study Start

September 16, 2024

Primary Completion

November 8, 2025

Study Completion

November 8, 2025

Last Updated

November 24, 2025

Record last verified: 2025-02

Data Sharing

IPD Sharing
Will not share

Locations