The Efficacy of PRUCARE Program and Pruritus
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Chronic Renal Insufficiency
- Itch
- Pruritus
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Supportive Care
Participation Requirements
- Age
- Between 18 years and 65 years
- Gender
- Both males and females
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 stu...
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.
Tracking Information
- NCT #
- NCT04289038
- Collaborators
- Baskent University
- Investigators
- Principal Investigator: NE?E ALTINOK ERSOY, PHDC Hacettepe University
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