Cannulation-Related Pain in Dialysis Patients With Arteriovenous Fistula
- Conditions
- Hemodialysis Access
- Registration Number
- NCT06236867
- Lead Sponsor
- Sülayman YAMAN
- Brief Summary
It was conducted to investigate the effect of ice application to the kaleidoscope and hoku point on the management of cannulization-related pain in patients receiving hemodialysis treatment.
- Detailed Description
After obtaining the necessary permissions for the research, the patients who were followed up in the hemodialysis unit of X,Y, Z Hospitals were randomly divided into three groups (Kaleidoscope application, ice application and control group).
Patients were made to sign written voluntary consent forms by the researchers.After the patients were transferred to the randomized program for the arrival days and TC numbers for the dialysis session, they were assigned to the experimental and control groups.
The patients' pain levels were evaluated during 3 dialysis sessions.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 102
Comfortable reception of trill and murmur sound from arteriovenous fistula,
• over the age of 18 and no communication problems,
- Having a place and time orientation,
- No dizziness,
-
Hemodialysis of the patient with arteriovenous graft and/or central venous catheter
-
Pharmacological application was made to relieve pain 30 minutes before AVF cannulation,
- The patient has a COVID - 19 infection
- Having visual, auditory and intellectual disabilities,
- Having a communication problem,
- Not willing and willing to participate in the study, as well as wanting to withdraw from the study at any stage of the study
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method visual pain scale (min-max:0-10 point) (1 week= during 3rd dialysis sessions) One week= during 3rd dialysis sessions Evaluation of pain levels (minimum=0 points, maximum: 10 points) of experimental and control groups in the 1st, 2nd and 3rd dialysis sessions
The visual pain scale is minimum 0 and maximum 10 points. 0 means no pain, 10 means severe pain.
1. st dialysis session= Visual analog pain scores during cannulation were evaluated without any application.
2. nd and 3rd dialysis sessions: Ice application to the patient's hoku point was performed by the researcher for 1 min before the AVF cannulation procedure and during cannulation, and visual analog scale pain scores was filled in during cannulation.
Kaleidoscope application was performed to the patient for 5 minutes before AVF cannulation procedure and during cannulation. The visual analog scale pain score was filled in during cannulation.
Control Group:visual analog scale pain scores will be evaluated before, during and after AVF cannulation without any intervention after the procedure.
- Secondary Outcome Measures
Name Time Method Sociodemographic and disease-related characteristics through study completion, an average of 3rd month. Comparison of sociodemographic characteristics (age, gender) with visual pain scale scores of the experimental and control groups.
Comparison of disease-related characteristics \[Body mass index:weight and height will be combined to report BMI in kg/m\^2 (weight in kilograms, height in meters=kg/m2), duration of dialysis (months), artery and vein needle size (14,15,16,17 gauge), duration of fistula use, region where the fistula is located)\] with visual pain scale scores of the experimental and control groups.
NOTE:After the data in all dialysis centers were completed (within about three months), the analysis was performed.The evaluation of Ice Application and kaleidoscope application After 3rd dialysis session (after one week) Learning patient experiences regarding ice application and kaleidoscope application via Kaleidoscope Application Patient Experience Form, Patient Experience Form for Ice Application.
The answers of the participants to the questions in the evaluation forms (Kaleidoscope Application Patient Experience Form, Patient Experience Form for Ice Application) are presented as a percentage. They were asked to answer the questions asked in the form as "yes, no, partially".
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Trial Locations
- Locations (1)
Amasya University İnstitute of Health Sciences
🇹🇷Amasya, Merkez, Turkey
Amasya University İnstitute of Health Sciences🇹🇷Amasya, Merkez, Turkey