The effect of topical application of lipogel in hemodialysis patients
Not Applicable
Recruiting
- Conditions
- renal disease.Rapidly progressive nephritic syndrome
- Registration Number
- IRCT20191007045019N1
- Lead Sponsor
- Sari University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 120
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
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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.
- Secondary Outcome Measures
Name Time Method