Improving the Perception of Stress and Mutuality in Caregivers (MI-DEAR Study) of Migraine Patients With Depressive Symptoms Treated With Fremanezumab: A Prospective Real-life Observational Study to Evaluate Whether Fremanezumab Reduces the Impact on Caregivers and Increases Couple Reciprocity

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

To evaluate the reduction of emotional burden (measured by Relative Stress Scale-RSS) of caregivers of migraine patients with Depressive Symptoms after 6 months after the first injection of fremanezumab.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ PATIENTS

• Adult patients, male or female

• Diagnosis of migraine, with or without aura, or chronic migraine, according to the International Classification of Headaches (ICHD-3.)

• Diagnosis of migraine with onset at an age of less than 50 years

• Depressive symptoms in patients defined as a Patient Health Questionnaire PHQ-9 scale score ≥5

• Complete details of migraine history and frequency of monthly migraine days in the past month

• clinical indication to start fremanezumab therapy to prevent migraine in patients naïve to monoclonal antibodies targeting the CGRP pathway

• In case of migraine preventive therapy and concomitant antidepressants, stability for at least 8 weeks prior to enrollment.

• Presence of a caregiver (see definition below) of the patient

• 80% compliance with diary and ability to complete the scale to provide written informed consent.

⁃ INFORMAL CAREGIVERS:

• Adult subjects, male or female.

• Informal caregiver is defined as a person--spouse/partner, parent, child/child, sibling--who cares for the migraine patient, sharing the same household and performing various functions, from basic daily needs to socio-economic activities)

• RSS score ≥ 1

• 80% compliance with completion scale ability to provide written informed consent

Locations
Other Locations
Italy
Ospedali Riuniti Umberto I- GM LANCISI G.SALESI
RECRUITING
Ancona
PO Avezzano S.Filippo e Nicola
RECRUITING
Avezzano
Clinica Neurologica L. Amaducci Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
RECRUITING
Bari
IRCCS Istituto Scienze Neurologiche
RECRUITING
Bologna
ASST Spedali Civili Brescia
RECRUITING
Brescia
Fondazione IRCCS Istituto Neurologico Carlo Besta
RECRUITING
Milan
Dipartimento delle scienze avanzate mediche e chirurgiche, Università della Campania Luigi Vanvitelli
RECRUITING
Naples
Fondazione Policlinico Universitario Campus Bio-Medico
RECRUITING
Rome
IRCCS San Raffaele Pisana
RECRUITING
Rome
Ospedale Fabenefratelli- San Pietro
RECRUITING
Rome
Contact Information
Primary
Claudia Altamura, MD, PhD
c.altamura@policilnicocampus.it
+3906225411270
Backup
Luisa Fofi, MD
l.fofi@policlinicocampus.it
Time Frame
Start Date: 2024-10-03
Estimated Completion Date: 2026-03-30
Participants
Target number of participants: 300
Treatments
PATIENTS
Adult male or female patients with diagnosis of migraine, with or without aura, or chronic migraine, according to the International Classification of Headaches (ICHD-3.)
CAREGIVER
Adult subjects, male or female who are informal caregiver of enrolled migraine patients, defined as a person--spouse/partner, parent, child/child, sibling--who cares for the migraine patient, sharing the same household and performing various functions, from basic daily needs to socio-economic activities)
Related Therapeutic Areas
Sponsors
Collaborators: Teva Pharmaceuticals USA
Leads: Fondazione Policlinico Universitario Campus Bio-Medico

This content was sourced from clinicaltrials.gov