asthma. Predominantly allergic asthma
Conditions
Interventions
Intervention 1: Patients in the control group routine care referral center include the period (2 months) under the doctor's clinic and receive medication adjustments. Intervention 2: Patients in the e
Patients in the control group routine care referral center include the period (2 months) under the doctor's clinic and receive medication adjustments.
Patients in the experimental group received acupressure also receive routine care center. In the experimental group, Chinese acupressure on the ST36 (in the anterior part of the leg and within the wid
Sponsors
Research Center School of Nursing and Midwifery, Tehran
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: - Inclusion criteria: In this study, all subjects in addition to the informed consent must also meet the following conditions. 1) younger than 65 and older than 18 years. 2) have an incentive to participate in the study. 3) The disease is confirmed by the medical experts and the results of diagnostic tests. 4) lowering medications such as amantadine not use fatigue. 5) disease is not known psychological and psychiatric drugs affecting their consumption. 6) the ability to understand their conversation in Farsi. 7) are literate. 8) the possibility of establishing direct telephone contact with the patients' residence there. - Exclusion criteria: 1) consent to continue participating in each stage of intervention. 2) the absence of the patient in the two sessions of acupressure 3) During the study, the disease progresses or the patient dies.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fatigue. Timepoint: Before the study, 4 and 8 weeks after the start of the study. Method of measurement: ???????? fss.;Quality of life. Timepoint: Before the study, 4 and 8 weeks after the start of the study. Method of measurement: Sf36 questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Second-hand smoke. Timepoint: Before the intervention. Method of measurement: Questions demographic questionnaire.;Type tobacco And duration of use. Timepoint: Before the intervention. Method of measurement: Questions demographic questionnaire.;Time to quit smoking. Timepoint: Before the intervention. Method of measurement: Questions demographic questionnaire.;Number of cigarettes smoked per day. Timepoint: Before the intervention. Method of measurement: Questions demographic questionnaire.;Smoking habits. Timepoint: Before the intervention. Method of measurement: Questions demographic questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShadan Pedramrazi
Tehran University of Medical Sciences,School of Nursing and Midwifery
Outcome results
None listed