renal disease. Rapidly progressive nephritic syndrome
Conditions
Interventions
Intervention 1: first Intervention group: After obtaining informed consent, during the hemodialysis while the patient in the test group lay on the bed, a same person removed 5% of the Lavogula Lavende
Sponsors
Sari University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Willingness to participate in the study 18 years of age or older End-stage kidney disease treated regularly with dialysis at least three times a week for six months with full alertness and ability to communicate, literate
Exclusion criteria
Exclusion criteria: no history of allergies ( skin and respiratory allergies essential oils and fragrances) no history of mental illness, lack of mental disorders(such as Down syndrome and dementia), lack of experience of any stressful event in the past six months (such as death of a close relative), lack of sedative medication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improve sleep quality. Timepoint: Before the intervention and four weeks after the intervention. Method of measurement: The quality of sleep with the Pittsburgh Instrument.;Feeling Well Using the yield Mental Feeling Tool. Timepoint: Before the intervention and four weeks after the intervention. Method of measurement: the instrument of yield feeling psychologically well. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHedayat Jafari
Sari University of Medical Sciences
Outcome results
None listed