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Effectiveness of treatment for chronic tension headache by the general practitioner or manual therapist: pilot study for a randomized clinical trial

Conditions
chonic tension headache
tension headache
10028302
10019231
Registration Number
NL-OMON30066
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

Chronic tension headache according to the classification of the International Headache Society (IHS), age 18-65 year, able to complete written questionnaires in Dutch; informed consent.

Exclusion Criteria

Reumatic diseases, fever, pregnancy, possibility of malignancy, manual therapy for chronic tension headache in preceding 2 months.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The baseline assessment includes a questionnaire regarding general health,<br /><br>headache, and medication use, limitations in daily functioning, and an<br /><br>assessment of the mobility of the cervical spine (using a Cervical Range Of<br /><br>Movement goniometer). Furthermore, an algometer will be used to measure tender<br /><br>points of the m trapezius descendens.<br /><br><br /><br>Outcomes are assessed after treatment (8 weeks) en after 26 weeks. Primary<br /><br>outcome measures are 1) frequency of headache (headache diary) and 2)<br /><br>medication use (diary).</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secundary outcome measures are: perceived recovery, limitations in daily<br /><br>activities, mobiilty of the cervical spine, and tender points of the m.<br /><br>trapezius descendens. </p><br>
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