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临床试验/NCT07199166
NCT07199166尚未招募不适用

Effectiveness of Autobiographical Rewriting Workshops on the Socio-Professional Functioning of Patients With Borderline Personality Disorder Undergoing Third-Wave Cognitive and Behavioral Therapy: A Randomized Controlled Trial

University Hospital, Montpellier0 个研究点目标入组 140 人开始时间: 2025年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
140
主要终点
Improvement in Social Functioning

研究概览

简要总结

This study evaluates the effectiveness of autobiographical rewriting workshops combined with third-wave Cognitive Behavioral Therapy (CBT) in improving social and professional functioning in individuals with Borderline Personality Disorder (BPD). BPD affects approximately 2 to 6% of the general population and is frequently associated with suicidal behaviors, unstable relationships, and low self-esteem. This disorder is often linked to early traumatic experiences that impact autobiographical memory and self-perception. While Dialectical Behavioral Therapy (DBT) is a standard treatment for BPD, it does not fully address all the needs of patients.

The aim of this study is to determine whether autobiographical rewriting, which allows individuals to restructure and reinterpret their memories in a more resilient way, can improve autobiographical memory, self-esteem, and reduce emotional symptoms. Participants will be randomized into two groups: one group will undergo autobiographical rewriting workshops in addition to third-wave CBT sessions, while the other group will participate in non-specific writing sessions also in addition to third-wave CBT sessions. The study will compare the two groups to evaluate the effectiveness of autobiographical rewriting workshops in enhancing social and professional well-being.

Expected outcomes include improvements in interpersonal relationships, greater professional stability, and a reduction in emotional symptoms assessed immediately post-intervention, then 3 months and 6 months after. This study may offer a complementary therapeutic approach to existing treatments, helping patients manage their symptoms more effectively and improve their quality of life.

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
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects with borderline personality disorder (assessed by SCID-2),
  • Subjects aged between 18 and 45 years (inclusive).

排除标准

  • Psychotic disorder (assessed by SCID),
  • Subjects deprived of their liberty (by judicial or administrative decision, or involuntary hospitalization),
  • Subjects under legal protection (guardianship, curatorship, or judicial protection),
  • Subjects not affiliated with a social security,
  • Pregnant or breastfeeding women,
  • Inability to understand the nature, purpose, and methodology of the study,
  • Inability to understand, speak, or write French,
  • Failure to provide informed oral consent to participate in the study.

结局指标

主要结局

Improvement in Social Functioning

时间窗: immediate post-intervention

The change in the score on the Social Functioning Questionnaire (SFQ) will be assessed between pre-intervention and post-intervention immediately, and compared between the two groups. The SFQ measures social functioning over the past two weeks, with 16 items divided into 8 domains: professional activities, daily life tasks, leisure, family and couple relationships, extrafamily relationships, financial and administrative management, general health, and community life and information. For each domain, participants assess the frequency and satisfaction of their activities

次要结局

  • Autobiographical Memory(6 months post-intervention)
  • Improvement in Social Functioning(6 months post-intervention)
  • Borderline Symptom Severity(6 months post-intervention)
  • Self-Concept Clarity(6 months post-intervention)
  • Self-Defining Future Projections(6 months post-intervention)
  • Self-Esteem(6 months post-intervention)
  • Reflective Emotions (Shame)(6 months post-intervention)
  • Sense of Coherence(6 months post-intervention)
  • Self-Representation (Ontological Addiction Scale)(6 months post-intervention)

研究者

申办方类型
Other
责任方
Sponsor

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