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| ID | Type | Description | Link |
|---|---|---|---|
| 2010-A00118-31 | Other Identifier | ANSM |
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| Name | Class |
|---|---|
| Fondation Apicil | OTHER |
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In patients with MOH, we will evaluate the impact of educative telephone coaching on the number of days with headache over the month preceding the appointment. The educative coaching will be administered by a nurse, during a single phone call and prior to the medical visit
In tertiary centers, it is not unusual for patients to wait for 6 months for a medical appointment. This clinical trial is monocentric, open, randomised. In the first arm, the patients will receive educative telephone coaching at Month 2 by the nurses, over the phone. In the second arm, the patients will not receive any educative telephone coaching before the appointment with the neurologist.
All patients will complete "Quality of life" questionnaires at Month 1 and Months 6, complete a migraine agenda during the length of the study and have a medical appointment around Month 6.
The primary outcome will be the efficacy of such educative telephone coaching, administered before the medical appointment in the Chronic Pain Center, in Bordeaux. It will be measured by the number of days with headache over the month preceding the appointment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 2 | No Intervention | no educative telephone coaching (ETC) | |
| 1 | Experimental | with educative telephone coaching (ETC) |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| educative telephone coaching (ETC) | Behavioral | a 30 to 45 minutes phone call, by appointment, by the nurse |
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| Measure | Description | Time Frame |
|---|---|---|
| To evaluate the efficacy of educative telephone coaching administered by the center's nurses prior to the medical on-site visit. | within 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| To evaluate the efficacy of educative telephone coaching (ETC) on the frequency of headaches and on the number of days with crisis treatment intake. | within 6 months | |
| To evaluate the efficacy of ETC on the patients quality of life and their handicap (emotional, professional and familial data) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Geneviève Chene, MD PhD | University Hospital, Bordeaux | Study Chair |
| Virginie Dousset, MD | University Hospital, Bordeaux | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Douleur Chronique - Groupe Hospitalier Pellegrin - Bât USN Tastet Girard | Bordeaux | 33076 | France |
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| ID | Term |
|---|---|
| D008881 | Migraine Disorders |
| ID | Term |
|---|---|
| D051270 | Headache Disorders, Primary |
| D020773 | Headache Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
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| within 6 months |
| To evaluate the patient's satisfaction toward ETC | within 6 months |
| To evaluate the patient's knowledge concerning migraine, medication overuse headache and their treatment after ETC | within 6 months |
| To estimate the cost/benefits ratio of ETC and its impact on medical costs ahead of the medical appointment. | within 6 months |
| D009422 | Nervous System Diseases |