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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03499392
Other study ID # P/2017/344
Secondary ID
Status Recruiting
Phase N/A
First received January 16, 2018
Last updated April 9, 2018
Start date April 30, 2017
Est. completion date September 30, 2018

Study information

Verified date March 2018
Source Centre Hospitalier Universitaire de Besancon
Contact Rose-Angélique BELOT
Phone 0680188113
Email rose-angelique.belot@univ-fcomte.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The World Health Organization (WHO) ranks headache among the top 20 causes of disability in the world.

Primary headaches (with no known organic cause) account for 90% of these conditions. INSERM estimates that 15% of the general population is concerned. WHO estimates that 1.7-4% of the global adult population is affected by headache for at least 15 days a month. Headaches are disabling, for patients (pain, suffering, fatigue, unavailability ...) but also for society (socio-economic cost as frequent work stoppages and drug costs). They are a public health problem.

In 2002, the High Authority of Health published its recommendations for the diagnosis and management of migraine patients. In addition, the French Society for Migraine and Headache Studies updated these recommendations in 2013. They are focused on the medical management offered by doctors and pharmacists. However, the professionals in daily contact with the subjects know that the dimension psychic plays an important role in the etiology of headaches.


Description:

The review of the literature shows the keen interest and the need for this type of research to better understand the main psychological factors involved in primary headaches.

The current vagueness, the lack of knowledge regarding the aspects associated psychological and the lack of studies on the French population can be filled with this study which takes place at the University Hospital of Besançon.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date September 30, 2018
Est. primary completion date April 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria:

- first consultation in neurology good general somatic state

Exclusion Criteria:

- Pregnancy History of psychiatric disorder

Study Design


Intervention

Other:
psychological tests
psychological tests psychological interviews

Locations

Country Name City State
France Belot Besançon Doubs

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of headache attacks Symptomatic evolution assessed with a composite outcome (number of episodes + severity of headaches) reported by patient and collected during neurological consultation Month 9
Primary Duration of each headache attack Symptomatic evolution assessed with a composite outcome (number of episodes + duration of each episode) reported by patient and collected during neurological consultation Month 9
Secondary Definition of patient's psychological profile Profile is determined by additional semi-structured interviews + Rorschach test + Adult Attachment Interview + mini-Social cognition and Emotional Assesment test (qualitative outcomes). Month 9
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