- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06545188
Impact of Mortality Salience on Treatment Decisions (MOST-D)
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Harmful overtreatment is a major problem in oncology. Unconscious fear of death (mortality salience) could increase the likelihood of a physician or patient decision in favor of aggressive therapy and thus contribute to overtreatment.
Methods: Conduction of two randomized controlled trials: 1. online survey of n = 260 urological patients, 2. paper questionnaire survey of n = 260 urological cancer inpatients. Intervention group: triggering of mortality salience with two open questions on death, control group: two open questions on dental treatment. The primary endpoint is the probability of opting for aggressive treatment in three questions on a treatment decision Likert scale from 0 to 10). In both studies, the evaluation is carried out as a comparison of means using a two-sided t-test. Secondary endpoints are further factors associated with a decision in favor of aggressive therapy.
Result: An increase in the probability of a decision in favor of the more aggressive therapy as a result of triggering mortality salience is expected with an effect size of d = .35.
Discussion: In order to avoid harmful overtreatment due to unconscious fear of death, doctors could undergo training to deal with their existential fears - this could take place as part of communication training. For cancer patients, this confrontation can take place as part of psycho-oncology training.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Düsseldorf, Germany, 40225
- University Hospital Düsseldorf, Department of Urology
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Study 1) Urologists
Inclusion Criteria:
- sufficient cognitive ability
- German language skills
Exclusion Criteria:
- none
Study 2) Patients
Inclusion Criteria:
- 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
Exclusion Criteria:
- none
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mortality salience trigger
Mortality Attitudes Personality Survey (MAPS, Rosenblatt et al. 1998) will be administered (two open questions about death and mortality)
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Two open questions about death and mortality will bei administered to trigger mortality salience
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Other: Dental pain questions (control condition)
Two open questions about a dental treatment will be administered
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Two open questions about a dental treatment (control condition)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
treatment decision
Time Frame: Day 0
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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 Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Operationalised Psychodynamic Diagnosis (OPD) structure questionnaire, OPD-SQ (Ehrenthal et al., 2015)
Time Frame: Day 0
|
12 items, 5-point likert scale, sum score 0 (high level of structure) to 48 (low level of structure) (Ehrenthal et al., 2012)
|
Day 0
|
|
Relationships-Revised Questionnaire, ECR-RD8 (Ehrenthal et al., 2021)
Time Frame: Day 0
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two subscales: attachment-related avoidance (4 items) and attachment-related anxiety (4 items), 8 items total, 7-point likert scale, sum score from 0 to 48 (higher values correspond to a higher expression of the dimension)
|
Day 0
|
|
Meaning in Life Questionnaire, MLQ (Steger et al., 2006)
Time Frame: Day 0
|
two subscales: search for meaning (5 items) and presence of meaning (5 items), 10 items total, 7-point likert scale, sum score form 5 to 35 per scale with lower levels indicating higher expression of the dimension)
|
Day 0
|
|
Peace of Mind Scale, POMS (Lee et al., 2013)
Time Frame: Day 0
|
7 items, 5-point likert scale, sum score form 7 to 35 (higher levels indicate more peace of mind)
|
Day 0
|
|
Death Attitude Profile - Revised, DAP-GR
Time Frame: Day 0
|
five subscales: fear of death (7 items), death avoidance (5 items), neutral acceptance (5 items), approach acceptance (10 items), escape acceptance (5 items), 35 items total, 7-point likert scale, an average value is calculated for each subscale by dividing the sum score of the domain by the number of its items
|
Day 0
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Urologists - socio-demographics
Time Frame: Day 0
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age (years), gender (male, female, other), relationship status (yes, no), children (yes, no), underage children living in the same household (yes, no)
|
Day 0
|
|
Urologists - job related factors
Time Frame: Day 0
|
professional experience (years), position (chief physician, senior physician, specialist, assistant physician), place of work (hospital, practice, both, other)
|
Day 0
|
|
Urologists - Effort-Reward-Imbalance Questionnaire - short version, ERI (short version) (Siegrist et al., 2009)
Time Frame: Day 0
|
Three subscales: Effort (7 items), reward (3 items), work stress (6 items), 16 items total, 4-point-likert scale (1 to 4), sum scores for each domain with higher levels corresponding to higher expression of the dimension
|
Day 0
|
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Patients - (modified) psycho-oncological basic documentation, PO-Bado (Herschbach et al., 2004)
Time Frame: Day 0
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gender (male, female, other), partnership (yes, no) children (yes, no), underage children living in the same household (yes, no), work situation (employed, on sick leave, housework, pension, unemployed, other [free text]), metastases (yes, no, unknown), date of first diagnosis (month/year, unknown), current disease status (first disease, second disease, relapse, remission, unknown), treatments in the last two months (surgery, radiation, chemotherapy, other systemic therapy / drug treatment for cancer (e.g.
immunotherapy), hormones, none, other [free text]), other relevant physical illnesses (yes, which?
Immunotherapy), hormones, none, other [free text]), other relevant physical illnesses (yes, which?
[free text], no, not known), psychotropic drugs / opiates (yes, which?
[free text], no, not known), psychological / psychiatric treatment in the past?
(yes, no, not known)
|
Day 0
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Patients - socio-demographics
Time Frame: Day 0
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age (years), education (no school-leaving certificate, primary school leaving certificate, secondary school leaving certificate ('Hauptschule' or 'Realschule'), Polytechnical high school 10th grade (before 1965: 8th grade), technical secondary school leaving certificate, high school diploma, I have another school-leaving certificate, namely: [free text])
|
Day 0
|
|
Patients - European Health Literacy Survey 16, HLS-EU-Q16 (Röthlin et al., 2013)
Time Frame: Day 0
|
Four dimensions: accessing, understanding, assessing and using health information, 16 items, four response categories are binarized (1 = "very easy / "fairly easy"; 0 = "very difficult" / "fairly difficult") and added together to form a total score: "adequate" (13-16 points), "problematic" (9-12 points) and "inadequate" (1-8 points).
|
Day 0
|
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Patients - Patient Health Questionnaire 9, PHQ-9 (Kroenke et al., 2001)
Time Frame: Day 0
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A total score (0 - 27 points) is calculated from nine items on a four-point Likert scale.
The following grading can be used: 0 - 4 points: minimal depressive symptoms, 5 - 9 points: mild depressive symptoms, 10 - 14 points: mild depressive symptoms, 15 - 19 points: moderate depressive symptoms, 20 - 27 points: severe depressive symptoms.
|
Day 0
|
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Patients - Generalized Anxiety Disorder 7, GAD-7 (Löwe et al., 2008)
Time Frame: Day 0
|
A total score (0 - 21 points) is calculated from seven items, each with a four-point Likert scale.
The threshold value for increased anxiety is 10 points.
|
Day 0
|
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Patients - Short form of the Fear of Progression Questionnaire (FoP-Q-SF) (Mehnert et al., 2006)
Time Frame: Day 0
|
The questionnaire comprises 12 items with a five-point Likert scale, from which a total score of 12 to 60 points can be calculated.
Moderate progressive anxiety is present if more than 50 % of the questions are answered with "often" or "very often", high progressive anxiety with more than 75 % of the questions.
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Day 0
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Patients - fear of cancer recurrence
Time Frame: Day 0
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Fear of cancer recurrence, FCR-1r (Smith et al., 2023) 1 item, scale from 0 (no fear of recuurence) to 10 (high fear of recurrence) |
Day 0
|
|
Patients - Concerns about Recurrence Questionnaire-4, CARQ-4 (Thewes et al. 2015)
Time Frame: Day 0
|
The first three items are rated on an 11-point Likert scale from 0 to 10. Item 4 asks for the subjective probability of cancer recurrence (0 to 100), which is then converted to a 0-10 scale.
Thus, the total score ranges from 0 to 40, with scores of 12 or higher indicating elevated fear of cancer recurrence levels.
|
Day 0
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Dominik Fugmann, Dr. med., Heinrich Heine University Duesseldorf, Germany
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GFFU Heigl Foundation 82301
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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