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Clinical Trials in Turkey / NCT07387497
Starting soon Not applicable

Palm Stimulator Use During Peripheral Venous Catheterization

NCT07387497 · tracked via the Priya Life Science Turkey tracker
Sponsor
Zeliha CENGİZ
Phase
Not applicable
Started
2026-02-20
Last updated
2026-02-06

Condition(s) studied

Procedural PainCancerFear NeedlesAnxietyCatheterization, Peripheral Venous

Investigational drug(s) / intervention(s)

Palm Stimulator Group

Palm Stimulator Group: 1-2 minutes before the procedure, patients will receive a brief orientation regarding the device. 20 seconds before PVC insertion, the device will be placed in the palm of the non-procedural hand. Patients will grip the device as the nurse applies the tourniquet. The tactile stimulation will continue throughout the needle entry and catheter stabilization.

Study summary

Purpose: The purpose of this study is to evaluate the effectiveness of a "Palm Stimulator" (a handheld device with blunt protrusions) in reducing pain, fear, and anxiety during peripheral venous catheterization (IV insertion) in adult cancer patients receiving chemotherapy.

Methods: This is a randomized controlled clinical trial. Participants will be randomly assigned to either the Experimental Group or the Control Group.

Experimental Group: During the IV insertion process, patients will hold and squeeze the Palm Stimulator in the palm of their non-procedural hand. The device is designed to provide intense tactile (touch) stimulation based on the "Gate Control Theory." Control Group: Patients will receive the standard routine care for IV insertion without any additional intervention.

Data Collection: Pain intensity will be measured using the Visual Analog Scale (VAS), while fear and anxiety levels will be assessed through VAS scales before and after the procedure. Patient satisfaction with the device will also be recorded.

Expected Outcome: The investigators hypothesize that the use of the Palm Stimulator will significantly decrease procedural pain and fear while increasing patient satisfaction compared to standard care. This study aims to provide a low-cost, non-pharmacological, and easy-to-use tool for oncology nurses to improve patient comfort during invasive procedures.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Aged 18-65 years. * Receiving chemotherapy treatment via peripheral venous catheter (PVC). * Cognitively capable of communicating and responding to pain, fear, and satisfaction scales. * Volunteering to participate and providing written informed consent. Exclusion Criteria: * Diagnosis of chemotherapy-induced peripheral neuropathy or diabetic neuropathy. * Presence of active infection, open wound, scar tissue, or edema in the palm. * Use of analgesic medication within 4-6 hours before the procedure. * History of hemiplegia or movement restriction in the extremity to be used for the procedure.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Turgut Ozal Medical Center Malatya Malatya

More Zeliha CENGİZ trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07387497 on ClinicalTrials.gov ↗ ← All trials in Turkey