Condition 1: Back pain. Condition 2: Hemodialysis. Dorsalgia, unspecified Preparatory care for renal dialysis
Conditions
Interventions
Intervention 1: Intervention group: The intervention will be such that the researcher will press the UB23-GB25-DU4 points, which are effective in reducing back pain, in the experimental group after be
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
Male
Age
60 Years to No maximum
Inclusion criteria
Inclusion criteria: Age over 60 years and older Having the ability to communicate verbally Being aware of place, time and people Willingness to participate in research Not using painkillers 24 hours before dialysis At least 3 months of hemodialysis experience Not using other complementary medicine methods to reduce back pain The absence of a wound or any supply in the pressure area that would make the intervention difficult The onset of chronic back pain at least 3 months after the start of the hemodialysis process The ability to lie on the stomach Getting a score of at least 3 on the Visual Analogue Scale (VAS) Samples being male Not having diseases such as spinal hernia, lumbar tumors, lumbar injuries and skin diseases such as shingles The completeness of the files of the patients participating in the research
Exclusion criteria
Exclusion criteria: Unwillingness to continue participating in the research program Patient withdrawal from the dialysis treatment is no more information program
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The score obtained in the standard instrument of visual pain scale (VAS). Timepoint: Before the intervention and before the start of the first hemodialysis session, and after the intervention and after the third hemodialysis session. The number of sessions for this intervention is 3 sessions, 2 days apart (first day - third day - fifth day). Method of measurement: Standard Visual Pain Scale (VAS) tool. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAbbas shamsalinia
Babol University of Medical Sciences
Outcome results
None listed