Comparison of the effects of reflexology massage and stroke on patients with bronchial asthma

INTERVENTION: Intervention 1: Reflexology massageThe patients in this group are selected according to the inclusion criteria after completing the questionnaire, and their FEV1 and respiratory rate are measured in four sessions (once a week) before and after reflexlogy massage . The signs are checked at the beginning and the end of the intervention. The reflexology massage is performed for 15 minutes. Intervention 2: stroke massage;The patients in this group are selected according to the inclusion criteria after completing the questionnaire, and their FEV1 and respiratory rate are measured in four sessions (once a week) before and after stroke massage . The signs are checked at the beginning and the end of the intervention. The reflexology massage is performed for 10 minutes. Intervention 3: Control group: Do not get an intervention. CONDITION: Bronchial asthma. ; Asthma PRIMARY OUTCOME: Oxygen saturation. Timepoint: Before and after intervention in each session. Method of measurement: Pulse oximeter. Respiratory rate in one minute. Timepoint: Before and after intervention in each session. Method of measurement: Clinical examination. The volume of air that is exerted by pressure in the first second from the lungs is measured as a percentage, the breathing rate per minute,. Timepoint: Each session is measured before and after intervention. Method of measurement: Spirometer. SECONDARY OUTCOME: Daily cough (more than twice a week). Timepoint: Before the intervention and at the end of the intervention (in the final session). Method of measurement: Questionnaire according to severity classification of asthma. Overnight cough 3‐4 times a month, 1 time or more per week. Timepoint: Before the intervention and at the end of the intervention (in the final session). Method of measurement: Questionnaire according to severity classification of asthma. Restricted activity. Timepoint: The beginning of the intervention before the intervention and the end of the intervention in the final session of the study. Method of measurement: Questionnaire according to severity classification of asthma. Shortness of breath 1 times per year due to shortness of breath / twice and more admitted due to shortness of breath,. Timepoint: Before the intervention and at the end of the intervention (in the final session). Method of measurement: Questionnaire according to severity classification of asthma. INCLUSION CRITERIA: Age between 18 and 65 years; No cognitive, hearing, and visual impairment; Ability and willingness to participate in the study; no use of drugs or psychotropic substances; Definite diagnosis of mild to moderate sustained asthma according to the physician’s opinion for more than 1 year; Forced expiratory volume in 1 second (FEV1) >60% or <95%; No hematologic disease such as hemophilia, reduced platelet, and deep vein thrombosis (DVT); No other treatments such as relaxation and psychotherapy.