An Online Self-management Intervention for Patients With Hand Fibromyalgia - a Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 70
- 试验地点
- 2
- 主要终点
- Change in pain coping
研究概览
简要总结
This study has been previously registered with the National Trial Registry (NTR6267) that has been cancelled. The registered trial has been automatically transferred to a new "Landelijk Trial Register", which does not contain all correct information on the current study and where no corrections can be made. Hence, the current study has been registered again with ClinicalTrials.gov.
The goal of this clinical trial is to study the effectiveness of an internet-based self-management intervention in adult patients with fibromyalgia. A randomized controlled trial (RCT) will be performed, in which 70 participants will be randomized to either the self-management intervention or a waitlist control condition (patients in the waitlist condition will receive the intervention after the intervention ends in the intervention group, i.e., after 6 months). The primary effect constitutes of the difference in change in pain coping between patients in the intervention and control condition from baseline to post-intervention. As secondary outcomes, a number of other psychological and physical outcome measures will be assessed (e.g., health-related quality of life, well-being, pain impact on daily life, pain cognitions). Also, cost-effectiveness of the intervention and the quality of the therapeutic relationship will be measured.
详细描述
Rationale: Fibromyalgia has a high clinical burden, with patients experiencing considerable pain, physical disability, and an often decreased health-related quality of life (HR-QoL). Improving patients' skills in managing a chronic condition ("self-management") is increasingly recognized as vital in the treatment of somatic conditions and is becoming more common in clinical practice and research. In this study, the effectiveness of an internet-based self-management intervention focusing on coping skills related to chronic pain compared with a waitlist control condition is studied.
Objective: To study the effectiveness of the internet-based self-management intervention in patients with fibromyalgia.
Study design: An RCT will be performed, in which 70 patients will be randomized to either the internet-based self-management intervention or a waitlist control group. Baseline, post-intervention, 6-week, and three-month follow-up questionnaires will be used to measure primary and secondary outcomes.
Study population: Patients ≥18 years diagnosed with fibromyalgia (confirmed by their general practitioner or a medical specialist) who visit the 'Fibrocentrum', a fibromyalgia treatment centre in Leiden, The Netherlands, will be invited to participate in the study. Patients need to have a pain duration of a minimum of 3 months, be fluent in Dutch, be able to give informed consent, and own a computer with internet access. Difficulties with (written) communication and internet literacy, severe physical and psychiatric comorbidities that interfere with the study protocol (e.g., addiction, psychosis, and suicidal ideation), pregnancy, on-going psychological treatment elsewhere, and participation in other clinical trials are exclusion criteria.
Intervention: The cognitive-behavioral intervention begins with a face-to-face intake session in which personal goals for the intervention are set. Afterwards, the tailored self-management intervention, consisting of 6 modules, will be offered via an internet-based program. The first introductory module includes goal-setting and the last module includes relapse prevention; the four modules in between focus on learning how to cope with the consequences of a chronic condition in daily life. The topics of the modules are (1) activity, (2) mood, (3) thoughts, and (4) the social environment. At least once a week, a psychologist provides participants with feedback and motivational support through messages in a secured mail box in the internet-based program. After finishing the internet-based intervention, two booster sessions will take place via telephone (1 month and 2,5 months after the program). Patients will be called by their psychologist and their goals will be evaluated and strategies to strengthen the achieved results will be discussed.
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
盲法说明
Blinding of participants and practitioners is not possible due to the nature of the study. However, the statistician who creates the randomization schedule and performs statistical analyses is blinded to group allocation.
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosed with fibromyalgia, as previously confirmed by their treating general practitioner or a medical specialist.
- •Pain complaints with a minimal duration of 3 months.
- •Minimum age of 18 years.
- •Fluent in Dutch.
- •Able to give informed consent.
- •Own a computer with internet access.
排除标准
- •Difficulties with (written) communication (e.g., due to analphabetism) and with internet literacy.
- •Severe physical and psychiatric comorbidities that interfere with the study protocol, such as psychosis, addiction, suicidal ideation.
- •On-going psychological treatment elsewhere.
- •Participation in other clinical trials.
研究组 & 干预措施
Internet-based self-management intervention
At the beginning of the treatment, a face-to-face introductory meeting is scheduled between the participant and a psychologist, where treatment goals will be set. Afterwards, a tailored self-management intervention, based on cognitive-behavioral methods, will be offered via an internet-based program. The psychologists offering the treatment have been trained in the tailored cognitive-behavioral protocol. One month and 2,5 months after finishing the online program, patients will be contacted by their treating psychologist for two booster sessions via telephone. Patients' goals will be evaluated and strategies to strengthen the achieved results will be discussed.
干预措施: Internet-based self-management intervention (Behavioral)
Waitlist
Patients in the control condition will be assigned to a waiting list and will receive the internet-based self-management intervention after the active treatment group (after 6 months).
结局指标
主要结局
Change in pain coping
时间窗: Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.
A visual analogue scale (VAS) from 0 to 10 will be used to measure pain coping, with higher scores indicating better pain coping. The primary endpoint is the difference in change in pain coping between patients in the intervention and control condition from baseline to post-intervention (immediately after the intervention).
次要结局
- Change in well-being(Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.)
- Change in pain coping strategies(Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.)
- Change in fibromyalgia impact(Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.)
- Change in illness cognitions(Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.)
- Change in pain(Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.)
- Change in pain interference in daily functioning and pain severity, and as exploratory measures support, life control, and affective distress(Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.)
- Change in Illness Perceptions(Baseline, immediately after the intervention, at 6 weeks and 3 months follow-up.)
- Change in health-related quality of life(Baseline, immediately after the intervention, at 3 months follow-up.)
研究者
Andrea W.M Evers, PhD
Professor
Leiden University
