Skip to content

Effects of Shotblocker and Manual Pressure on Pain and Satisfaction

Effects of Shotblocker and Manual Pressure on Pain and Satisfaction During Peripheral Venous Catheter Placement: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06947525
Enrollment
81
Registered
2025-04-27
Start date
2025-04-28
Completion date
2025-06-30
Last updated
2025-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Satisfaction

Brief summary

This study aims to determine the effects of shotblocker and manual pressure applied during peripheral venous catheter placement on pain and satisfaction. 81 patients hospitalized in the Urology clinic will be included in the study. Patients will be assigned to three groups as shotblocker (n=27), manual pressure (n=27) and control group (n=27) by block randomization method. Research Hypotheses * H1-1: The mean pain scores of the intervention group to which shotblocker was applied during peripheral intravenous catheterization are different from the control group. * H1-2: The mean pain scores of the intervention group to which manual pressure was applied during peripheral intravenous catheterization are different from the control group. * H1-3: The mean satisfaction scores of the intervention group to which shotblocker was applied during peripheral intravenous catheterization are different from the control group. * H1-4: The mean satisfaction scores of the intervention group to which manual pressure was applied during peripheral intravenous catheterization are different from the control group.

Interventions

Before the procedure in the manual pressure group, the vein entry area will be pressed with the right hand thumb for 10 seconds. The pressure will be applied until the nail bed turns white.

OTHERShotblocker

In the Shotblocker group, the shotblocker will be placed 2 cm above the vein entry point and will remain throughout the procedure.

Sponsors

Necmettin Erbakan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Admission to the urology clinic, * No verbal, perceptual and visual communication problems, * Between the ages of 18 and 65, * Literate, * Volunteer to participate in the study, * Not using medication that will create a chronic analgesic effect, * Not having chronic or acute pain, * No intervention has been performed on the vein where the PIC is placed in the last month, * No scar tissue or infection in the areas where the PIC will be placed, * Not having a disease that will cause problems in feeling pain (such as neuropathy)

Exclusion criteria

* The individual wants to leave the study, * Feels unwell during the PIC placement (such as dizziness, palpitations), * Uses sedatives or alcohol,

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale (VAS)The peripheral venous catheter will be filled within 1 minute after insertion.The minimum score on the scale is 0 and the maximum score is 10. A score of 0 indicates no pain, while a score of 10 indicates unbearable pain.

Secondary

MeasureTime frameDescription
Patient Satisfaction ScaleThe peripheral venous catheter will be filled within 1 minute after insertion.It is a horizontal scale that can be scored between 0 and 10. It is a measurement tool that starts with I am not satisfied at all - 0 - I am very satisfied - 10 and ends with.The minimum score on the scale is 0 and the maximum is 10. A score of 0 indicates that the procedure is not satisfactory at all, while a score of 10 indicates that the procedure is very satisfactory.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026