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临床试验/NCT07534930
NCT07534930进行中(未招募)不适用

Personalised Multidisciplinary Multimodal Treatment in IBS

Linkoeping University1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年9月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
150
试验地点
1
主要终点
IBS symptom severity score

研究概览

简要总结

This is a 12-month longitudinal intervention study in adults (18-65 years) with moderate-severe IBS (IBS-SSS ≥175) evaluating a personalized, patient-centered multidisciplinary treatment delivered in a Swedish tertiary care setting. The program includes an internet-based IBS school followed by four evidence-based modules (physician-led medical management/education, dietician-led dietary intervention, psychologist-led IBS-focused behavioral therapy, and physiotherapy) delivered in a sequence chosen by the participant, with symptom evaluation after each module. Outcomes are assessed before and after treatment, with the primary endpoint defined as treatment response (IBS-SSS reduction ≥50 points), and secondary endpoints covering symptom/psychological measures, visceral sensitivity and biological stress plus gut biomarkers, and multimodal brain imaging (structural MRI, rs-fMRI, task fMRI, and insula MRS).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

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

入选标准

  • IBS diagnosis confirmed according to the Rome IV criteria
  • Moderate-to-severe symptoms based on the IBS Symptom Severity Score (IBS-SSS)
  • Age 18-65 years
  • Written informed consent.

排除标准

  • Contraindications to MRI, e.g., claustrophobia, pregnancy, or metallic implants.
  • History of major gastrointestinal surgery, e.g., appendectomy.
  • Severe psychiatric illness, such as bipolar disorder or schizophrenia.
  • Insufficient Swedish language knowledge to complete the questionnaires

研究组 & 干预措施

Multidisciplinary multimodal intervention (IBS)

Active Comparator

Single-arm intervention: all participants are assigned to a multimodal, multidisciplinary IBS treatment program delivered by a multidisciplinary team. No control group was included due to the nature of the study.

干预措施: Physician-module (Other)

Multidisciplinary multimodal intervention (IBS)

Active Comparator

Single-arm intervention: all participants are assigned to a multimodal, multidisciplinary IBS treatment program delivered by a multidisciplinary team. No control group was included due to the nature of the study.

干预措施: Dietician module (Other)

Multidisciplinary multimodal intervention (IBS)

Active Comparator

Single-arm intervention: all participants are assigned to a multimodal, multidisciplinary IBS treatment program delivered by a multidisciplinary team. No control group was included due to the nature of the study.

干预措施: Psychologist module (Other)

Multidisciplinary multimodal intervention (IBS)

Active Comparator

Single-arm intervention: all participants are assigned to a multimodal, multidisciplinary IBS treatment program delivered by a multidisciplinary team. No control group was included due to the nature of the study.

干预措施: Physiotherapy module (Other)

结局指标

主要结局

IBS symptom severity score

时间窗: From enrollment through 1 year after completion of multimodal, multidisciplinary treatment.

The primary outcome was treatment response, defined as a reduction of ≥50 points in the IBS Symptom Severity Score (IBS-SSS). Participants achieving this reduction were classified as responders.

次要结局

  • Changes in Gastrointestinal symptom severity(Baseline, 3, 6, 9, and 12 months)
  • Psychological symptom burden(At the baseline, 3 months, 6 months, 9 months and end of intervention (12 months))
  • Visceral sensitivity index (VSI)(Baseline, 3, 6, 9, and 12 months)
  • Changes in Gut-brain axis physiology(Baseline and 12 months.)
  • Brain imaging outcomes - Brain Structure(At the baseline and after 12 months.)
  • Brain imaging outcomes - Brain neurochemistry(Baseline and 12 months.)
  • Brain imaging outcomes - Brain function (BOLD signal activity)(Baseline and 12 months.)
  • Serum vasoactive intestinal peptide (VIP) and inflammatory marker concentrations(Baseline and 12 months.)

研究者

发起方
Linkoeping University
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Susanna Walter

MD, PhD and Adjunct Professor

Ostergotland County Council, Sweden

研究点 (1)

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