Tension-Type Headache
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age between 20 and 30 years; Nulliparous and nulliparous; For the group with headache: women with clinical diagnosis of migraine or episodic tension-type headache, performed by a neurologist, through anamnesis and neurological examination, based on the diagnostic criteria of the ICDH; Body Mass Index (BMI) <30kg / m² (WORLD HEALTH ORGANIZATION, 2011); Will be included in the migraine group, women diagnosed with migraine with aura, without aura or both, probable migraine or migraine associated with tension-type headache; Women who do not present with severe heart disease, neurological diseases, disabling musculoskeletal diseases, cognitive problems or those with clinical conditions of instability that imply risk and / or inability to participate in the training program;
Exclusion criteria
Exclusion criteria: Chronic migraine or chronic tension-type headache; Women with low adherence to training (frequency less than 75% of sessions in a one-month period) will be excluded; pregnancy; Drug or alcohol abuse; Use of antipsychotic or antidepressant medications;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Decreased Frequency (days) of headache verified through the migraine diary from the comparison of the pre and post intervention averages. Student's t test will be used with a level of significance set at 5% (p <0.05).;Expected outcome 2: Decreased intensity (pain scale from 0 to 10) of the headache verified through the migraine diary from the comparison of the pre and post intervention averages. Student's t test will be used with a level of significance set at 5% (p <0.05).;Expected outcome 3: Decreased duration (hours) of the headache verified through the migraine diary from the comparison of the pre and post intervention averages. Student's t test will be used with a level of significance set at 5% (p <0.05).;Expected outcome 4: Improved cardiorespiratory fitness measured by maximal oxygen consumption (VO2), obtained by the ventilatory method. Student's t test will be used with a level of significance set at 5% (p <0.05) for pre and post intervention comparison. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Universidade Federal de Pernambuco