跳至主要内容
临床试验/NCT05082922
NCT05082922进行中(未招募)不适用

Implementation of a Transdiagnostic Emotion-focused Treatment for Comorbid Emotional Problems and Chronic Pain in Clinical Care. A Sequential Replicated and Randomized Single Case Experimental Design (SCED).

Örebro University, Sweden2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
50
试验地点
2
主要终点
Patient Health Questionnaire (PHQ-9) change

研究概览

简要总结

In society today, mental health problems, specifically stress-, anxiety- and depressive disorders, are a primary cause of long-term sick leave, leading to significant societal costs and suffering. One important issue hindering implementation of successful treatments is that there is a marked co-occurrence between these problems and somatic health problems, such as different types of pain. An important key to solving this problem is to develop a more integrated conceptualization of, and treatment model for, these patients' health problems. Specifically, one way to understand the co-occurrence between mental and somatic health problems is offered by the 'transdiagnostic' perspective. The aim of this project is to implement and evaluate the effectiveness of a transdiagnostic emotion-focused treatment protocol in clinical context. The treatment addresses comorbid mental (stress, anxiety- and depressive) and somatic health (pain) problems and targets core emotion regulation processes that are hypothesized to maintain and exacerbate these problems.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Data is collected using a secure digital platform. Outcome assessors will be blinded to baseline length allocations.

入排标准

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

入选标准

  • > 11 points on the anxiety or depression subscale, Hospital Anxiety and Depression scale
  • somatic health problems (pain > 3 months) with functional impairment (>3 on question 2 of the Multidimensional Pain Inventory, MPI, OR > 20 points on question 21-24 of the Örebro Musculoskeletal Pain Questionnaire, ÖMPQ)

排除标准

  • severe psychiatric problems requiring immediate other treatment
  • current psychological treatment
  • recently started psychopharmacological treatment for anxiety or depression (<3 months prior to planned treatment)
  • insufficient mastery of the Swedish language

结局指标

主要结局

Patient Health Questionnaire (PHQ-9) change

时间窗: repeated weekly through phase A (randomly assigned to be 4, 5 or 6 weeks) and treatment phase B (14 to 16 weeks). Total time frame of assessment is 20 weeks.

change in self rated depression. Scale range 0-27 (higher values worse outcome)

Pain change

时间窗: repeated weekly through phase A (randomly assigned to be 4, 5 or 6 weeks) and treatment phase B (14 to 16 weeks). Total time frame of assessment is 20 weeks.

change in pain intensity (scale 0-6) and interference. Scale range 0-6 (higher values worse outcome)

Generalised Anxiety Disorder (GAD-7) change

时间窗: repeated weekly through phase A (randomly assigned to be 4, 5 or 6 weeks) and treatment phase B (14 to 16 weeks). Total time frame of assessment is 20 weeks.

change in self rated anxiety. Scale range 0-27 (higher values worse outcome)

Symptom Catastrophizing Scale (SCS) change

时间窗: Baseline, 5 months and 11 months as well as repeated weekly through phase A (randomly assigned to be 4, 5 or 6 weeks) and treatment phase B (14 to 16 weeks). Total time frame of assessment is 20 weeks.

Change in catastrophic interpretation of symptoms. Scale range 0-14 (higher values worse outcome)

Pain coping change

时间窗: repeated weekly through phase A (randomly assigned to be 4, 5 or 6 weeks) and treatment phase B (14 to 16 weeks). Total time frame of assessment is 20 weeks.

change in pain worry (scale 0-6) and avoidance (scale range 0-8) (higher values worse outcome)

次要结局

  • Psychological Inflexibility in Pain Scale (PIPS) change(Baseline, 5 months and 11 months)
  • Mini international neuropsychiatric interview (MINI)(Baseline, 5 months)
  • EQ5-D change(Baseline, 5 months and 11 months)
  • Montgomery Åsberg Depression Rating Scale (MADRS) change(Baseline, 5 months and 11 months)
  • Difficulties in Emotion Regulation Scale (DERS-16) change(Baseline, 5 months and 11 months)
  • Work limitation questionnaire-16 change(Baseline, 5 months and 11 months)
  • Multidimensional Pain Inventory (MPI) change(Baseline, 5 months and 11 months)
  • Insomnia Sleep Inventory (ISI) change(Baseline, 5 months and 11 months)

研究者

发起方
Örebro University, Sweden
申办方类型
Other
责任方
Sponsor

研究点 (2)

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