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NCT07029126Completed

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

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

Source: ClinicalTrials.gov · Last updated 2 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
308 (actual)
First submitted
10 Mar 2025
Start date
3 Oct 2024
Primary completion date
30 Mar 2026
Lead sponsor
Fondazione Policlinico Universitario Campus Bio-Medico
Diseases
Migraine
NCT number
NCT07029126

What you commit to

  • Study type: Observational
  • Participants enrolled: 308
  • From 3 Oct 2024 to the primary completion date, 30 Mar 2026
  • 10 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • The patient has clinically significant hematological, cardiac, renal, endocrine, pulmonary, gastrointestinal, genitourinary, neurologic, hepatic, ocular disease, or complications of an infection, at the discretion of the investigator
  • Patient with a clinical history of a severe or uncontrolled psychiatric disorder (bipolar disorders, schizophrenia, psychosis), at the discretion of the investigator, that would likely interfere with full participation in the study
  • History of migraine.
  • History of major depressive disorder and severe or uncontrolled psychiatric disorder (bipolar disorders, schizophrenia, psychosis), at the discretion of the investigator, that would likely interfere with full participation in the study
  • The caregiver has clinically significant hematological, cardiac, renal, endocrine, pulmonary, gastrointestinal, genitourinary, neurologic, hepatic, ocular disease, or complications of an infection at the discretion of the investigator.

Other

  • Patients:
  • Patients without a caregiver
  • Contraindications or lack of indication to fremanezumab
  • Patient participating in another study at the same time as enrollment in the current study
    • Informal Caregivers:

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ospedali Riuniti "Umberto I"- GM LANCISI G.SALESI
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AnconaItalyUnknown status
PO Avezzano "S.Filippo e Nicola"
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AvezzanoItalyUnknown status
Clinica Neurologica "L. Amaducci" Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
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BariItalyUnknown status
IRCCS Istituto Scienze Neurologiche
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BolognaItalyUnknown status
ASST Spedali Civili Brescia
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BresciaItalyUnknown status
Fondazione IRCCS Istituto Neurologico Carlo Besta
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MilanItalyUnknown status
Dipartimento delle scienze avanzate mediche e chirurgiche, Università della Campania "Luigi Vanvitelli
Coordinator of this site? Confirm its status
NaplesItalyUnknown status
IRCCS San Raffaele Pisana
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RomeItalyUnknown status
Ospedale Fabenefratelli- San Pietro
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RomeItalyUnknown status
Fondazione Policlinico Universitario Campus Bio-Medico
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RomeItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.