Sleep disorders. Sleep disorders
Conditions
Interventions
Intervention 1: Group 1 intervention: Sedamin capsule containing 530 mg of valerian root was fed for two weeks and every two days, one morning and one night, and once a week for two weeks, the Pittsbu
Treatment - Drugs
Group 1 intervention: Sedamin capsule containing 530 mg of valerian root was fed for two weeks and every two days, one morning and one night, and once a week for two weeks, the Pittsburg Questionnaire
Lavender essence that every night 2 drops of pure essential oil are peeled and inhaled for 15 days and every other night
The third group was the control group. After completing the demographic questionnaire, no intervention was performed and Pittsburgh sleep quality questionnaire completed weekly for two weeks.
Sponsors
Vice chancellor for research, Aja University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Criteria for entering the study: age over 18; awareness of time and place; lack of hearing impairment, vision (in such a way that it can not communicate with the investigator); lack of mental retardation; lack of drug addiction; lack of Allergy to flowers; lack of olfactory disorder; absence of respiratory and respiratory problems such as asthma; non-use of any drugs; hypnotic judgment; individual benzodiazebel; patient; no acute problem during admission; no history of anxiety and depression according to findings Patients have read and write skills. The lack of use of various complementary therapies during the last three months was passed. At least 24 hours of hospitalization. Exit criteria: Acute problem during admission or absence of stable and stable hemodynamic conditions; Failure to cooperate during the study; Over 75 years of age; Use of sleep medication; Mental and psychological crisis, mourning and divorce; Lavender smell sensitivity ; Failure to perform the application of the herbal remedy more than 3 times a week for any reason; Not taking the use of Sodamine capsule for 7 days; The history of surgery in recent months.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| High blood pressure. Timepoint: Before the intervention, the first week of intervention, the second week of intervention. Method of measurement: manometer.;Increase of heart rate. Timepoint: Before the intervention, the first week of intervention, the second week of intervention. Method of measurement: manometer.;Chest pain. Timepoint: Before the intervention, the first week of intervention, the second week of intervention. Method of measurement: See. | — |
Secondary
| Measure | Time frame |
|---|---|
| Fatigue.morning. Timepoint: 40/5000 ??? ????? ??? ??? ???: ??? ?? ??????? ???? ??? ? ???? ??? ?????? Before the intervention, first week and second week of intervention. Method of measurement: Pittsburgh Questionnaire.;Sleepiness daily. Timepoint: Before the intervention, first week and second week of intervention. Method of measurement: Pittsburgh Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShahla Aliyari
AJA University of Medical Sciences
Outcome results
None listed