The Efficacy of PRUCARE Program and Pruritus
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- STATUS
- Recruiting
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- participants needed
- 40
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- sponsor
- Hacettepe University
Summary
The research will be conducted randomly in order to determine the effect of PRUCARE program structured according to the biopsychosocial itch model in the management of itch symptom.
Description
In this study, there will be three groups: intervention group 1 with training, counseling and autogenic relaxation (OR), intervention group 2 with training, counseling and virtual reality game application and control group with routine nursing care. The number of volunteers to be included in the study was determined by power analysis. Forty patients with itch symptoms will be included in each group. Preliminary application for all three groups will be performed in the patient group registered to the Dialysis Unit of the Nephrology Department of Hacettepe University and Baskent University Hospital. Socio-Demographic Form, 5-D Itch Scale, Visual Analogue Scale (VAS), Dermatology Life Quality Index, State and Trait Anxiety Scale, Pruritus Behavior and SGO / OR Application Log, Dietary Behavior of Hemodialysis Patients Scale, Hemodialysis Patients Diet Information Scale and Digital Skin Moisture Measurement Device will be used.
Details
Condition | Pruritus, chronic renal insufficiency, Renal Failure, Renal Failure, Chronic renal failure, Dermatosis |
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Age | 18-65 years |
Treatment | prucare program |
Clinical Study Identifier | NCT04289038 |
Sponsor | Hacettepe University |
Last Modified on | 19 February 2024 |
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