Sequential, Multiple Assignment, Double Randomized Preference, Migraine Behavioral Trial

Part of paid clinical trials in Phoenix, Arizona.

Sponsor
Mayo Clinic
Study ID
NCT06170281
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Migraine Behavioral Treatment — BEHAVIORAL
    Migraine Behavioral Treatment involving daily activities

Study Details

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.

Key Dates

Start date
Dec 31, 2026
Status verified
Jun 2026
Primary completion
Jul 1, 2028
Completion
Dec 1, 2028

Study Design

Enrollment
24 participants (estimated)
Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Random - ME
    participants will be randomized to an intervention involving regular mealtime and regular timed exercise
  • Active Comparator: Random - MS
    participants will be randomized to an intervention involving regular mealtime and regular sleep
  • Active Comparator: Random - SE
    participants will be randomized to an intervention involving regular sleep and regular timed exercise
  • Active Comparator: Choice - ME
    this arm belongs to participants who choose the intervention involving regular mealtime and regular timed exercise
  • Active Comparator: Choice - MS
    this arm belongs to participants who choose the intervention involving regular mealtime and regular sleep
  • Active Comparator: Choice - SE
    this arm belongs to participants who choose the intervention involving regular sleep and regular timed exercise

Primary Outcome Measure

Feasibility in terms of recruitment and adherence rates [ Time Frame: 12 weeks ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Mayo ClinicPhoenixArizona85054
Yohannes W. Woldeamanuel, MD
480-342-1385

Find similar trials in Phoenix, AZ

By condition
By specialty

Related Studies