Q-MIGAL: Validation of a Questionnaire for Allodynia in Migraine.

Sponsor
University Hospital, Clermont-Ferrand (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04580641
Collaborator
(none)
180
14
11
12.9
1.2

Study Details

Study Description

Brief Summary

Migraine is very frequent (15% of the general population). During attacks, many subjects with migraine have allodynia (pain induced by normally non-painful stimuli), photophobia (hypersensitivity to light), phonophobia (hypersensitivity to sound) or osmophobia (hypersensitivity to odours). The goal of the present study is to validate a new questionnaire made of 4 parts evaluating the presence of these 4 types of hypersensitivity, both during or between migraine attacks. It will allow to look for associations of these 4 symptoms and association of hypersensitivity with patients' or migraine's characteristics.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaire

Detailed Description

The prevalence of migraine is around 15% worldwide (GBD 2016, Lancet Neurol 2018). During attacks, and even between attacks, especially when migraine frequency is high, many subjects with migraine present with photophobia, phonophobia, osmophobia or allodynia. These symptoms are though to correspond to central sensitization and can be found in animal models of migraine (Boyer et al., Pain 2017; Dallel et al., Cephalalgia 2018).

These 4 symptoms have been studied separately in previous studies but to date, there is no overall questionnaire evaluating these 4 sub-types of hypersensitivity. The investigators have constituted a questionnaire based on previous validated questionnaires that have been translated into French (Lipton et al., 2008 for cutaneous allodynia; Choi et al., 2009 for photophobia), a previous questionnaire validated in French (Khalfa et al, 2002 for phonophobia) and created a few questions for each of the 4 symptoms, including osmophobia.

Study Design

Study Type:
Observational
Anticipated Enrollment :
180 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Allodynia and Sensorial Hypersensitivity in Patients With Migraine: Validation of a Specific Questionnaire
Anticipated Study Start Date :
Oct 1, 2020
Anticipated Primary Completion Date :
Jun 1, 2021
Anticipated Study Completion Date :
Sep 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Subjects with migraine

No medical intervention. All included subjects will filled in the questionnaire concerning migraine characteristics and associated symptoms.

Other: Questionnaire
A self-administered questionnaire will be completed by each study subject

Outcome Measures

Primary Outcome Measures

  1. Predictive factors of allodynia/hypersensitivity in subjects with migraine [baseline]

    Correlations between scores on specific questionnaires evaluating allodynia/hypersensitivity (cutaneous allodynia with the questionnaire by Lipton et al., 2008, osmophobia with a home-made questionnaire rated from 0 to 4, photophobia with the questionnaire by Choi et al., 2009, phonophobia with the questionnaire by Khalfa et al., 2002), patients characteristics (age, sex, Body mass index, habits, score on the Hospital Anxiety and Depression scale) and migraine characteristics (presence of aura or not, migraine duration in years, migraine frequency in attacks per month, pain intensity during migraine attacks rated from 0 to 4).

Secondary Outcome Measures

  1. Predictive factors of cutaneous allodynia in subjects with migraine [baseline]

    Correlations between score on the 12-item Allodynia Symptom Checklist (Lipton et al., 2008) (score from 0 to 24 with higher values indicating higher level of allodynia), patients characteristics (age in years, sex, body mass index in kg/m², consumption of alcohol and tobacco, score on the Hospital Anxiety and Depression scale) and migraine characteristics (presence of aura or not, migraine duration in years, migraine frequency in attacks per month, pain intensity during migraine attacks rated from 0 to 4) .

  2. Predictive factors of photophobia in subjects with migraine [baseline]

    Correlations between scores on two specific questionnaires evaluating photophobia (Choi et al., 2009; binary score for presence or absence of photophobia and home-made questionnaire with score from 0 to 4 with higher values indicating higher level of phonophobia), patients characteristics (age in years, sex, body mass index in kg/m², consumption of alcohol and tobacco, score on the Hospital Anxiety and Depression scale) and migraine characteristics (presence of aura or not, migraine duration in years, migraine frequency in attacks per month, pain intensity during migraine attacks rated from 0 to 4).

  3. Predictive factors of phonophobia in subjects with migraine [baseline]

    Correlations between scores on a questionnaire evaluating phonophobia (Khalfa et al. 2002, score from 0 to 42 with higher values indicating higher level of phonophobia), patients characteristics (age in years, sex, body mass index in kg/m², consumption of alcohol and tobacco, score on the Hospital Anxiety and Depression scale) and migraine characteristics, (presence of aura or not, migraine duration in years, migraine frequency in attacks per month, pain intensity during migraine attacks rated from 0 to 4).

  4. Predictive factors of osmophobia in subjects with migraine [baseline]

    Correlations between scores on a specific home-made questionnaire evaluating osmophobia (score from 0 to 4 with higher values indicating higher level of osmophobia), patients characteristics (age in years, sex, body mass index in kg/m², consumption of alcohol and tobacco, score on the Hospital Anxiety and Depression scale) and migraine characteristics (presence of aura or not, migraine duration in years, migraine frequency in attacks per month, pain intensity during migraine attacks rated from 0 to 4).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects fulfilling 2018 international headache society criteria for migraine.

  • Age > 17 years.

  • Written consent.

Exclusion Criteria:
  • Presence of neurological comorbidities that could lead to sensorial or sensitive abnormalities

  • Presence of dermatological comorbidities that could lead to sensorial or sensitive abnormalities

  • Presence of ENT comorbidities that could lead to sensorial or sensitive abnormalities

  • Significant cognitive dysfunction precluding proper completion of the self-administered questionnaire

Contacts and Locations

Locations

Site City State Country Postal Code
1 CH d'Annecy, Centre d'Etude et de Traitement de la Douleur Annecy France 74000
2 Cabinet de Neurologie Clermont-Ferrand France 63000
3 CHU de Clermont-Ferrand, Centre d'Etude et de Traitement de la Douleur Clermont-Ferrand France 63000
4 CHU de Clermont-Ferrand, Service de Neurologie Clermont-Ferrand France 63000
5 CH Emile Roux Le Puy en Velay, Service de Neurologie Le Puy-en-Velay France 43000
6 CHU de Lille, Service de Neurologie Lille France
7 CHU de Lyon, Hôpital Pierre Wertheimer, Service de neurologie fonctionelle et épileptologie Lyon France 69000
8 Assistance Publique - Hôpitaux de Marseille, CHU La Timone, Centre d'Evaluation et Traitement de la Douleur Marseille France 13000
9 CHU de Montpellier, Service de Neurologie Montpellier France 34000
10 CHU de Nantes, Service de Neurologie Nantes France 44000
11 CHU de Nice, Département Evaluation et Traitement de la Douleur Nice France 06000
12 Assistance Publique - Hôpitaux de Paris, CHU Lariboisière, Service de Neurologie Paris France 75000
13 CHU de Rouen, Service de Neurologie Rouen France 76000
14 CH de Vichy, Service de Neurologie Vichy France 03200

Sponsors and Collaborators

  • University Hospital, Clermont-Ferrand

Investigators

  • Principal Investigator: Xavier Moisset, MD, PhD, CHU de Clermont-Ferrand

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Clermont-Ferrand
ClinicalTrials.gov Identifier:
NCT04580641
Other Study ID Numbers:
  • RNI 2018 MOISSET (Q-MIGAL)
First Posted:
Oct 8, 2020
Last Update Posted:
Oct 8, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Clermont-Ferrand
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 8, 2020