Migraine Nervous System Diseases
Conditions
Interventions
Participants will be randomly assigned to the intervention or control group using a computer-generated randomization sequence created with the online randomization tool Randomizer.org. Participants wi
Sponsors
Université du Québec en Abitibi-Témiscamingue
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Canadian veterans living with migraine 2. Able to take part in a francophone online group 3. Consent to be part of the study
Exclusion criteria
Exclusion criteria: Does not meet the inclusion criteria
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| 1. Pain intensity and pain interference as well as broader health domains measured using PROMIS-29 Profile v2.0 at 0, 3, 6, 9 and 12 months 2. Functional impact of migraine on daily activities measured using the Headache Impact Test (HIT-6) at 0, 3, 6, 9 and 12 months 3. Migraine-specific quality of life measured using the Migraine-Specific Quality of Life Questionnaire (MSQ) at 0, 3, 6, 9 and 12 months 4. Participants’ perceived overall change in pain symptoms measured using the Patient Global Impression of Change (PGIC) at 3, 6, 9 and 12 months 5. Burden of migraine between headache episodes measured using the Migraine Interictal Burden Scale (MIBS-4) at 0, 3, 6, 9 and 12 months 6. Headache frequency: number of headache episodes recorded using a headache diary (paper calendar) or the Migraine Tracker application at 0, 3, 6, 9 and 12 months | — |
Countries
Canada
Contacts
Public ContactAnaïs Lacasse
Outcome results
None listed