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临床试验/NCT05785429
NCT05785429已完成不适用

The Effect of Colchicine on Food-related Effort-based Decision Making in Brain and Behaviour in Overweight and Obesity: the FLAIR-i Study

Donders Centre for Cognitive Neuroimaging1 个研究点 分布在 1 个国家目标入组 59 人开始时间: 2022年8月2日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
59
试验地点
1
主要终点
Change in effort valuation in brain and behaviour

研究概览

简要总结

The main objective of the FLAIR-i study is to study the causal role of inflammation in affecting effort-based decision making in brain and behaviour in overweight and obesity, by comparing the effect of the anti-inflammatory agent colchicine vs. placebo.

详细描述

Obesity is a major health problem worldwide and is characterized by increases in low-grade, systemic inflammation. Outside the field of obesity, increases in inflammation have been related to loss of motivation and effortful behaviour, which can be objectively measured with effort-based decision making in brain and behaviour. Here, the investigators hypothesise that low-grade inflammation is causing altered striatal brain responses and effortless 'fast food' choices in overweight and obesity. The objective of this study is to study the causal role of inflammation in affecting effort-based decision making in brain and behaviour in overweight and obese participants, by comparing the effect of the anti-inflammatory agent colchicine vs. placebo. In addition, it will be investigated whether this primary objective translates to more ecologically valid measures/settings.

研究设计

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

入排标准

年龄范围
18 Years 至 59 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • BMI ≥ 27 kg/m2
  • Female sex
  • Right-handed
  • Age: 18-59 years
  • Shoulder width of < 68 cm (to fit into the MRI scanner)
  • Dutch speaking - Sufficient level to understand task instructions
  • Low-grade inflammatory state, as measured by C-reactive protein (CRP) between 3.0 and 10.0 mg/L

排除标准

  • Having been vaccinated by any type of vaccine in the 4 weeks preceding the first test session
  • Having had an infection characterized by a fever, or diagnosed by a medical physician in the 4 weeks preceding the first test session
  • Diagnosed with Diabetes Mellitus type I or II
  • Gained or lost >2 points in BMI (kg/m2) over the last 6 months
  • Followed an energy restricting diet during the last 2 months
  • Having had bariatric surgery in the past 5 years
  • Regular use of anti-inflammatory, anti-diabetic, weight-loss, and psychoactive medication
  • Regular use of CYP3A4 inhibitors, P-glycoprotein inhibitors, statins, fibrates, ciclosporin, and digoxin, as a contraindication for colchicine
  • Have renal impairment as evidenced by serum creatinine >150 μmol/l or eGFR <50mL/min/1.73m2, determined maximum 12 weeks before inclusion
  • Have moderate to severe hepatic disease
  • (History of) clinically significant psychiatric or neurological disorder
  • (History of) clinically significant metabolic, cardiovascular, renal, liver, endocrinological, autoimmune or chronic inflammatory disease
  • General medical conditions, such as sensorimotor handicaps, deafness, blindness or colour-blindness, as judged by the investigator
  • Current or history of alcohol and/or drugs abuse (i.e. >14 units per week)
  • Habitual smoking, i.e. one or more cigarettes per day
  • Pregnant, lactating or wishing to become pregnant in the period between the screening and until 3 months after the last study visit
  • Participation in another weight loss, lifestyle or anti-inflammatory intervention in the context of research at the time of inclusion or during the study
  • Contraindications for MRI

研究组 & 干预措施

Colchicine

Experimental

One tablet of colchicine 0.5 mg per day

干预措施: Colchicine 0.5 MG (Drug)

Placebo

Placebo Comparator

One tablet of microcrystalline cellulose per day

干预措施: Placebo (Drug)

结局指标

主要结局

Change in effort valuation in brain and behaviour

时间窗: Change between baseline and follow-up after 12 weeks

Brain activity (BOLD signal during functional MRI) and behavioural weightings upon/of effort sensitivity, as measured by an effort-based decision making task.

Change in reward valuation in brain and behaviour

时间窗: Change between baseline and follow-up after 12 weeks

Brain activity (BOLD signal during functional MRI) and behavioural weightings upon/of reward sensitivity, as measured by an effort-based decision making task.

次要结局

  • Change in reward anticipation/reward consummation ratio in daily life(Change between baseline and follow-up after 12 weeks)
  • Change effort/reward related food intake ratio(Change between baseline and follow-up after 12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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