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A Quality of Life Study in Patients With Migraines

Dysphoric-like Disorder of Epilepsy, Is It Unique?

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00298805
Enrollment
52
Registered
2006-03-03
Start date
2006-01-31
Completion date
2013-04-30
Last updated
2013-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression, Headache, Migraine

Keywords

Migraine, Headache, Depression, Quality of Life

Brief summary

The purpose of this study is to compare depressive characteristics in migraine patients to those observed in patients with epilepsy in a previous study, and determine whether those symptoms are unique to patients with epilepsy.

Detailed description

A form of depression known as dysphoric-like disorder is common in people with epilepsy, which may significantly affect the quality of life in these people, as shown in a previous study. However, it is unclear if this depressive disorder is unique to patients with epilepsy. In order to assess whether these symptoms are unique and idiosyncratic to the epilepsy population, in this multi-center study, these dysphoric depressive features will be contrasted to those seen in patients with other neurologic or psychiatric conditions. Migraine is selected as one of the comparison disorders because it shares with epilepsy characteristics of being a recurrent episodic central nervous system disorder, and our site will only enroll patients with migraine headaches.

Interventions

None listed

Sponsors

Rush University Medical Center
CollaboratorOTHER
GlaxoSmithKline
CollaboratorINDUSTRY
Northwell Health
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female 18 years of age or older * Have the diagnosis of migraine * Have had no change in migraine medication(s) 30 days prior to study * Achieve a satisfactory score on the Wide Range Achievement Test 3 (WRAT3) test at the screening visit * Capable of completing self-reporting questionnaires * Willing and able to provide written informed consent and comply with the study protocol

Exclusion criteria

* Presence of a clinically significant comorbidity of an unstable or progressive nature * Presence of major depression * Participation in an investigational drug study within the past 30 days * Inability to communicate well with site study personnel

Design outcomes

Primary

MeasureTime frame
Dysphoric-like depressive characteristics in patient with epilepsyN/A (cross-sectional study)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026