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Clinical Trials/ACTRN12610000393055
ACTRN12610000393055
Recruiting
N/A

Evaluating an avoidance versus coping based approach to the behavioural management of triggers for migraine and tension-type headaches, by measuring the primary outcomes of: (a) daily headache activity; (b) headache medication use; and (c) impact of headache on daily living

Professor Paul Martin (Principal Investigator)0 sites180 target enrollmentMay 17, 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Migraines
Sponsor
Professor Paul Martin (Principal Investigator)
Enrollment
180
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 17, 2010
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Professor Paul Martin (Principal Investigator)

Eligibility Criteria

Inclusion Criteria

  • (i) diagnosed as either ‘migraine without aura’, ‘probable migraine without aura’, ‘typical aura with migraine headache’, ‘probable migraine with aura’, ‘chronic migraine’, ‘frequent episodic tension\-type headache’, probable frequent episodic tension\-type headache’, ‘chronic tension\-type headache’, ‘probable ergotamine\-overuse headache’, ‘probable triptan \-overuse headache’, ‘probable analgesic \-overuse headache’, ‘probable opioid\-overuse headache’, ‘probable combination analgesic\-overuse headache’, ‘headache probably attributed to overuse of acute medication combinations’, ‘headache probably attributed to other medication overuse\- Headache Classification Subcommittee of the International Headache Society (IHS), 2005; (ii) minimum of 6 headache days per month; (iii) minimum headache chronicity of 12 months, and pattern of headache symptoms stable over last 6 months.

Exclusion Criteria

  • (i) pregnant, planning pregnancy during trial period or lactating; (ii) currently taking headache prophylactic medication (one month wash\-out period required); (iii) currently receiving psychological or psychiatric treatment.

Outcomes

Primary Outcomes

Not specified

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