跳至主要内容
临床试验/NCT06170281
NCT06170281尚未招募不适用

A Feasibility Clinical Trial Assessing Patient Preference, Optimum Combinations and Sequences of a Multicomponent, Virtually-Delivered Migraine Behavioral Intervention

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2026年12月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
Mayo Clinic
入组人数
24
试验地点
2
主要终点
Feasibility in terms of recruitment and adherence rates

研究概览

简要总结

This study will unpack the behavioral intervention for migraine and determine the optimum combinations. In addition, the study will test preference and self-selection effects during the trial.

详细描述

After a 4-week screening period, eligible candidates (14 headache days in 4 week period, with 8 days being migraine) will be randomized into 2 arms -

  • Choice Arm: allowed to choose from a menu of migraine behavioral treatment options
  • Random: randomized to migraine behavioral treatment options.

After 6 weeks, all participants will be assessed for their migraine frequency. Patients will be considered Responders if the migraine frequency is reduced to 50%. The Non-responders (NR) of the Choice Arm will be again given a chance to pick any of the 3 arms. The NR of the randomized arm will be randomized to any of the 3 arms. The responders will continue for 6 more weeks in their original arms. By the end of the 12 weeks, all participants will complete the study, and migraine frequency will be compared between the different groups. All behavioral interventions will be delivered virtually.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

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

  • have chronic migraine for a minimum of 1-year
  • aged 18 years and older

排除标准

  • secondary headache disorders
  • children younger than 18 years old

研究组 & 干预措施

Choice - MS

Active Comparator

this arm belongs to participants who choose the intervention involving regular mealtime and regular sleep

干预措施: Migraine Behavioral Treatment (Behavioral)

Choice - SE

Active Comparator

this arm belongs to participants who choose the intervention involving regular sleep and regular timed exercise

干预措施: Migraine Behavioral Treatment (Behavioral)

Random - ME

Active Comparator

participants will be randomized to an intervention involving regular mealtime and regular timed exercise

干预措施: Migraine Behavioral Treatment (Behavioral)

Random - MS

Active Comparator

participants will be randomized to an intervention involving regular mealtime and regular sleep

干预措施: Migraine Behavioral Treatment (Behavioral)

Random - SE

Active Comparator

participants will be randomized to an intervention involving regular sleep and regular timed exercise

干预措施: Migraine Behavioral Treatment (Behavioral)

Choice - ME

Active Comparator

this arm belongs to participants who choose the intervention involving regular mealtime and regular timed exercise

干预措施: Migraine Behavioral Treatment (Behavioral)

结局指标

主要结局

Feasibility in terms of recruitment and adherence rates

时间窗: 12 weeks

recruitment rate, adherence rate

次要结局

  • Migraine Frequency(at baseline 4 weeks before randomization, week 2-6 after date of randomization, week 8-12 after date of randomization)
  • Headache Self-efficacy(at baseline 4 weeks before randomization, week 2-6 after date of randomization, week 8-12 after date of randomization)
  • Migraine Intensity(at baseline 4 weeks before randomization, week 2-6 after date of randomization, week 8-12 after date of randomization)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yohannes Woubishet Woldeamanuel

Principal Investigator

Mayo Clinic

研究点 (2)

Loading locations...

相似试验

Sequential, Multiple Assignment, Double Randomized... | 临床试验