Death Anxiety, Depression and Anxiety: An Experimental Study
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Mortality Salience Prompts, Dental Pain Prompts.
- Who it may be relevant to
- Registry conditions: Death Anxiety, Depression, Anxiety. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Romania
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Death Anxiety: Implications for Depression and Anxiety - An Experimental Study
Overview
The goal of this experimental study is to investigate the transdiagnostic role of death anxiety in depression and anxiety symptoms in participants from the general population. The main questions it aims to answer are: 1. Does the mortality salience task induce death anxiety? 2. Does the experimental group present an increase in depression and anxiety symptoms following the mortality salience task? The investigators will compare the experimental condition to a control condition to see if the death anxiety induction is responsible for the expected increase in depression and anxiety symptoms. The mortality salience prompt will be asking participants to elaborate on their thoughts and feelings surrounding death and dying, including what they think happens during death. The dental pain prompt will ask participants to do the same, only in regards to the thought of having dental pain. Experimental group: participants will undergo a pen-and-paper writing task where they will be asked to answer two questions: 1. "Please briefly describe the emotions that the thought of your own death arouses in you." 2. "Jot down, as specifically as you can, what you think will happen to you physically as you die and once you are physically dead." Control group: 1. "Please briefly describe the emotions that the thought of dental pain arouses in you." 2. "Jot down, as specifically as you can, what you think happens to you physically as you experience dental pain and once you have physically experienced dental pain."
Detailed description
The purpose of this study is to investigate the role of death anxiety as a transdiagnostic factor in psychopathology. In this particular study, the investigators will examine whether increases in death anxiety - brought about by increasing the salience of death by use of a mortality salience prime lead to increases in levels of depression and anxiety.
Participants will provide their informed consent and will proceed to complete the measures of the study (pretest). Eligible participants will be randomly allocated to either the mortality salience group (experimental group), or the dental pain group (the control group). Participants will be blind to group allocation.
Two weeks after completing the pretest measures, the participants will come to the lab and undergo the experimental tasks, depending on the condition that they have been allocated to.
Experimental group: participants will undergo a pen-and-paper writing task where they will be asked to answer two questions
1. Please briefly describe the emotions that the thought of your own death arouses in you. 2. Jot down, as specifically as you can, what you think will happen to you physically as you die and once you are physically dead.
Control group: participants will undergo a pen-and-paper writing task where they will be asked to answer two questions
1. Please briefly describe the emotions that the thought of dental pain arouses in you. 2. Jot down, as specifically as you can, what you think happens to you physically as you experience dental pain and once you have physically experienced dental pain.
After the prime, participants will complete a distractor task, during which they will be asked to read a short, emotionally neutral text - a bogus scientific article, estimated to be a 5 minute read - and answer questions based on this text. Participants will be told that this task is done in order to assess text comprehension abilities. After completing the distractor task, participants will complete the study measures the second time (posttest).
Upon study completion, all participants will be debriefed in the lab, and the real purpose of the study will be explained to them.
Interventions
- Behavioral Mortality Salience Prompts
This intervention implies giving two prompts to participants, in a written format, while asking them to write out answers to the given prompts. The first prompt is: "Please briefly describe the emotions that the thought of your death arouses in you." The second prompt is "Jot down, as specifically as you can, what you think will happen to you physically as you die and once you are physically dead." - Behavioral Dental Pain Prompts
This intervention implies giving two prompts to participants, and requesting that participants write out their answers to these prompts. The first prompt is: "Please briefly describe the emotions that the thought of dental pain arouses in you." The second prompt is: "Jot down, as specifically as you can, what you think happens to you physically as you experience dental pain and once you have physically experienced dental pain."
Primary outcome measures
- Collet-Lester Fear of Death Scale - Revised (CLFD-R) [Time frame: Baseline (Day 1), After the experimental task (Day 14)]
Secondary outcome measures (3)
- The Generalized Anxiety Disorder - 7 [Time frame: Baseline (Day 1), After the experimental task (Day 14)]
- Patient Health Questionnaire - 9 [Time frame: Baseline (Day 1), After the experimental task (Day 14)]
- State and Trait Anxiety Inventory - State subscale [Time frame: Baseline (Day 1), After the experimental task (Day 14)]
Eligibility criteria
Inclusion criteria
- Age over 18 years.
- Living in Cluj-Napoca (or otherwise willing and able to participate in the lab task)
Exclusion criteria
- Personality disorder diagnosis
- Psychotic disorder diagnosis
- Suicidal ideation
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Basic science
Study locations
Romania · 1 center
- Babes Bolyai University — Cluj-Napoca
Identifiers
NCT: NCT07201480 · 430/ 30.04.2024