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The Effectiveness of an Online Self-Delivered Death Anxiety Intervention

The Effectiveness of an Online Self-Delivered Death Anxiety Intervention: A Pilot Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06801132
Enrollment
47
Registered
2025-01-30
Start date
2025-02-14
Completion date
2025-04-04
Last updated
2026-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Death Anxiety

Keywords

Death Anxiety, randomized controlled trial, self-delivered

Brief summary

The goal of this clinical trial is to examine the effectiveness of the online self-delivered death anxiety intervention developed by our team in the general population with a randomized controlled trial. The study will recruit 50 participants, with 25 randomized to the death anxiety intervention group and 25 randomized to the control group (waiting list). The online intervention on death anxiety consists of 4 phases that take about 2 hours in total. The primary outcome DAS (Death Anxiety Scale) and DABBS (Death Anxiety Beliefs and Behaviors Scale) will be administered on baseline, post-treatment, 1-week follow-up, and 2-week follow-up assessments.

Interventions

BEHAVIORALOnline self-delivered death anxiety intervention

The online self-guided death anxiety intervention developed in this study is based on the Death Education and CBT framework. It took approximately two hours to complete the full intervention. The main content includes: 1. Emotional reactions and behavioral manifestations about death, fear management theories, and Chinese cultural attitudes toward death; 2. Imagine what you would like to say to yourself at the end of your life, and learn about various attitudes towards death through numerous examples; 3. Expressive writing, with moderate emotional exposure to stimulate reflection, accompanied by breathing exercises and positive thinking about death, to improve tolerance and control of death anxiety, and finally to correct biased perceptions by examining bad beliefs about death; 4. Prioritize the importance of things and make a practical action plan to enrich your life.

Participants assigned to WL will be asked not to use our death anxiety intervention or seek additional help related to death anxiety during the 1-week intervention period. After the one-month follow-up of the experimental group, the WL group will receive the same intervention for death anxiety. WL participants will also be given contact information to use in case of increasing distress.

Sponsors

Peking University
Lead SponsorOTHER
101 Institute, Ministry of Civil Affairs of the People's Republic of China
CollaboratorUNKNOWN

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

Randomization was conducted by an independent research assistant, and the random sequence was concealed from the investigator until the process was completed.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 18-65 years of age * Normal literacy skills and ability to use a smartphone proficiently * Higher death anxiety that is above the cutoff of our measurement * Voluntarily participate in this intervention and be able to provide informed consent.

Exclusion criteria

* Severe depressive state or risk of suicidal self-injury, i.e., the total score of Patient Health Questionnaire 9-item ≥19 or the score of 9th item ≥2 * Diagnosed within 6 months with schizophrenia, depression, bipolar disorder, and other psychiatric disorders * Have received any intervention for death anxiety or CBT intervention on any topic within the past 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Templer Death Anxiety Scale (T-DAS)baseline, post treatment (only for intervention group), 1 week, 2 weeksThe T-DAS consists of 15 items, describing the experiences that individuals feel when facing death. The Chinese version suggests a 5-point scale according to the later extended version of the scale, ranging from 1 "Strongly Agree" to 5 "Strongly Disagree", with higher scores representing more severe death anxiety. The higher the score, the more serious the death anxiety, and a total score greater than 43 according to the rules can be considered to have a high level of death anxiety. The Chinese version of T-DAS has been widely used and has shown good reliability and validity.
Death Anxiety Beliefs and Behaviors Scale (DABBS)baseline, post treatment (only for intervention group), 1 week, 2 weeksThe DABBS consists of 18 entries describing overall feelings about death (4 entries), thoughts and beliefs related to death (7 entries), and avoidance behaviors related to death (7 entries), with the scale being scored on a 5-point scale ranging from 1, "Strongly Disagree/Never Have This Thought/Never Avoid This Behavior" to 5 "Strongly agree/always have this thought/always avoid this behavior," with higher scores representing the severity of the individual's adverse beliefs and behaviors regarding death.

Secondary

MeasureTime frameDescription
Patient Health Questionnaire 9-itembaseline, 1 week, 2 weeksPatient Health Questionnaire 9-item (PHQ-9), a self-report measure for depressive symptoms in the past two weeks, comprises 9 items rated from 0 (not at all) to 3 (nearly every day). The PHQ-9 has good psychometric properties in Chinese adolescents.
Generalized Anxiety Disorder 7-itembaseline, 1 week, 2 weeksGeneralized Anxiety Disorder 7-item (GAD-7) scale is a 7-item self-report measure to assess anxiety symptoms in the past two weeks. Each item is rated from 0 (not at all) to 3 (nearly every day). The Chinese version GAD-7 score has good psychometric properties among adolescents.
Insomnia Severity Index (ISI)baseline, 1 week, 2 weeksThe ISI consists of seven items that assess the severity of subjective insomnia in the past two weeks, including, for example, difficulty in falling asleep, sleep satisfaction, impairment of daytime functioning, etc. The total score ranges from 0-28, with higher scores representing more severe insomnia. The Chinese version of ISI has been shown to have good reliability and validity.
4-dimensional anxiety scalebaseline, 1 week, 2 weeksThis is a 40-item scale for measuring multi-dimensional anxiety, which includes 4 dimensions (emotional, physiological, cognitive, and behavioral) and 9 subscales (emotional, psychosomatic, autonomic, general cognitive, phobia, over-committed, repetitive, social, and avoidance). The higher the score on this scale, the more severe the anxiety in a certain area.
Ryff's Psychological Well-being Scale (PWS)baseline, post treatment (only for intervention group), 1 week, 2 weeksThe short version used in this study contains 18 entries, including six dimensions of positive relations, autonomy, environmental mastery, personal growth, purpose in life, and self-acceptance. The six dimensions of self-acceptance are scored on a 6-point scale ranging from 1 "not at all" to 6 "very much", with higher scores representing higher psychological well-being. The Chinese version of PWS has been translated by Taiwanese scholars and has been proven to have Good reliability and validity.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026