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临床试验/NCT06810999
NCT06810999尚未招募不适用

From Fear to Purpose ACT Protocol: Testing Indirect, Transdiagnostic Implications of Death Anxiety Over Depression and Anxiety. A Randomized Placebo Controlled Trial.

Babes-Bolyai University0 个研究点目标入组 175 人开始时间: 2025年6月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
175
主要终点
Change from baseline Death Anxiety score to the follow-up moment (6 weeks duration)

研究概览

简要总结

The main purpose of this placebo controlled trial is to test the efficacy of a one-session From Fear to Purpose ACT intervention in reducing self-reported death anxiety levels. Another objective of this study is to investigate whether reductions in death anxiety levels are associated with reductions in depression and anxiety levels, thus testing if death anxiety is a transdiagnostic factor involved in psychopathology.

详细描述

This is a placebo controlled trial where the main objective is to test if the one-session From Fear to Purpose ACT intervention is effective in reducing self-reported death anxiety levels. A secondary objective is to investigate whether reductions in death anxiety levels are associated with reductions in depression and anxiety levels, thus testing if death anxiety is a transdiagnostic factor involved in psychopathology.

Participants will be selected based on death anxiety levels (moderate-high scores) and depression and anxiety symptoms (subclinical levels). Minors, people with suicidal ideation, people with current psychological/psychiatric diagnosis (excepting depression or anxiety diagnosis), people in active psychological/psychiatric treatment will be excluded. Recruited participants will be randomized into two groups: the experimental group (will receive the From Fear to Purpose ACT intervention) and the placebo group. The placebo condition will be undergoing a group-based attentional control activity. Participants will be blinded to the study condition.

The From Fear to Purpose intervention protocol is based on Acceptance and Commitment Therapy (ACT) strategies, build around identifying and committing to personal values. The intervention will be group-based (90 minutes session). The intervention will be administered by experienced psychotherapists.

The primary outcome is death anxiety, while secondary outcomes are depression and anxiety symptoms, well-being, psychological flexibility, experiential avoidance and valued living.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Moderate-high levels of death anxiety (score > or = 55) AND
  • •Subclinical levels of depression (score > or = 9) AND/OR
  • •Subclinical levels of anxiety (score > or = 9)

排除标准

  • •Suicidal ideation
  • •Current psychological/psychiatric diagnosis (except depression or anxiety diagnosis)
  • •Active psychological/psychiatric treatment

研究组 & 干预措施

Experimental Group

Experimental

This arm is the experimental group which will receive the intervention. The intervention is a one session From Fear to Purpose ACT Protocol, which is built on Acceptance and Commitment Therapy (ACT) strategies, focused on identifying and committing to personal values.

干预措施: From Fear to Purpose (Acceptance and Commitment Therapy) (Other)

Placebo Group

Placebo Comparator

This arm is the placebo group, which will be undergoing a group-based attentional control intervention.

干预措施: Placebo (Other)

结局指标

主要结局

Change from baseline Death Anxiety score to the follow-up moment (6 weeks duration)

时间窗: From enrolment to follow-up (6 weeks time frame)

Death anxiety measured with Death Anxiety Beliefs and Behaviours Scale (Menzies, Sharpe, Dar-Nimrod, 2022). Scores range from 18 to 90, with higher scores indicating higher death anxiety levels.

次要结局

  • Change from baseline Depression score to the follow-up moment (6 weeks duration)(From enrolment to follow-up (6 weeks time frame))
  • Change from baseline Anxiety score to the follow-up moment (6 weeks duration(From enrolment to follow-up (6 weeks time frame))
  • Change from baseline Well-being score to the follow-up moment (6 weeks duration)(From enrolment to follow-up (6 weeks time frame))
  • Change from baseline Psychological Flexibility to the follow-up moment (6 weeks duration)(From enrolment to follow-up (6 weeks time frame))
  • Change from baseline Experiential Avoidance score to the follow-up moment (6 weeks duration(From enrolment to follow-up (6 weeks time frame))
  • Change from baseline Valued Living score to the follow-up moment (6 weeks duration(From enrolment to follow-up (6 weeks time frame))

研究者

发起方
Babes-Bolyai University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Roxana Cardos

PhD

Babes-Bolyai University

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