Drug-induced headache. Drug-induced headache, not elsewhere classified
Conditions
Interventions
Intervention 1: The intervention is reflexology massage, the upper part of the patient's toe, the spot of reflection related to head will be massaged for both legs in the intervention group at two ste
Treatment - Other
Placebo
Touch will perform that is not linked to head will be massaged in the placebo group.
In intervention group acupressore will be done in hegu point for 2 minutes and rest for 2 minutes and this procidure was repeated for 10 minutes. At 15 minutes after the first intervention, the second
The intervention is reflexology massage, the upper part of the patient's toe, the spot of reflection related to head will be massaged for both legs in the intervention group at two steps for 20 minute
Sponsors
Shahed University Vice Chancellor For Research
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: willing to participate in the study; age between 18 to 65; The absence of verbal and visual disorders; The absence of sensory-motor disorders; The absence of advanced neurological disorders; The absence of clotting problems, peripheral vascular disease, peripheral neuropathy and DVT limb; The absence of diagnosed psychiatric disorder; The absence of a headache before the administration of Nitroglycerine; the absence of any history of headache in patients; not having an addiction to drugs, sedatives, alcohol; Not using analgesics and nerve- muscle blockers 4 hours before the intervention; not having a long history of taking Nitroglycerine; The absence of history of using reflexology or acupressure; Not using of steroidal and non-steroidal anti-inflammatory drugs, anticoagulation, chemotherapy. Exclusion criteria: Incidence of severe complications during the study; Pain in other parts of the body other than the head; the severity of the pain so that the patient can not tolerate; Use analgesics drugs during the study; Dissatisfaction of attending physician or patient.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of headache. Timepoint: Before the intervention , after the first intervention and after second intervention. Method of measurement: Visual Analog Pain Scale.;Quality of headache. Timepoint: Before the intervention, after the first intervention and after second intervention. Method of measurement: McGill Pain Questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Heart rate. Timepoint: Before the intervention, after the first intervention and after second intervention. Method of measurement: Monitoring system.;Systolic Blood pressure. Timepoint: Before the intervention, after the first intervention and after second intervention. Method of measurement: Monitoring system.;Diastolic blood pressure. Timepoint: Before the intervention, after the first intervention and after second intervention. Method of measurement: Monitoring system.;Mean blood pressure. Timepoint: Before the intervention, after the first intervention and after second intervention. Method of measurement: Monitoring system.;Respiratory rate. Timepoint: Before the intervention, after the first intervention and after second intervention. Method of measurement: Monitoring system.;Oxygen saturation of arterial blood. Timepoint: Before the intervention, after the first intervention and after second intervention. Method of measurement: pulse oximeter. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Nahid Rejeh
Shahed University
Outcome results
None listed