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Effect of Shotblocker and Palm Stimulator

N

Necmettin Erbakan University

Status

Completed

Conditions

Pain

Treatments

Other: palm stimulator
Other: shotblocker

Study type

Interventional

Funder types

Other

Identifiers

NCT06381804
24YL9001

Details and patient eligibility

About

This study discusses the advancements in nursing, particularly focusing on intramuscular injections, their complications, and innovative non-pharmacological methods such as the Shotblocker and palm stimulator to reduce pain. These methods, based on the gate control theory, aim to minimize discomfort during injections by applying tactile stimulation, which has proven effective in various studies.

Full description

It was planned to examine the effect of shot blocker and palm stimulator use on injection-related pain during intramuscular injection.This study is a randomized controlled, single-blind, parallel group experimental study to be conducted in the emergency department of a State Hospital in Konya, Turkey. The research will be conducted on individuals who will receive intramuscular (IM) injection. Participants will be randomized and divided into Shotblocker, Palm stimulator and control groups. Data collection will run from April 2024 to May 2024 and analyzes will be conducted blinded by an independent statistician. This study aims to evaluate the effects of these techniques on pain and anxiety.

Enrollment

96 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Volunteering to participate in the research,

    • Those who will receive vitamin B injection ordered by physician due to B12 deficiency,
    • Conscious and oriented,
    • Able to understand and speak Turkish,
    • Age range is between 18-65,
    • Having no vision or hearing problems,
    • Pain score of 2 or less when evaluated with a visual analog scale,
    • Able to lie in the right lateral position where injection can be administered,
    • Those who have not had an IM injection into the right ventrogluteal area in the last week,
    • Body mass index is within the normal range (25.0-29.9 kg/m2) according to WHO,
    • Those who have not used any analgesics or muscle relaxants in the last 24 hours,
    • Does not have any problems such as hardness, mass, edema or infection in the area to be injected,
    • According to his own statement, he has no psychiatric diagnosis,

Exclusion criteria

  • Having pain anywhere in the body,

    • Narcotic type or different analgesic area before application,
    • Pregnant or suspected of pregnancy,
    • Individuals in menstrual period,
    • Receiving chemotherapy and radiotherapy treatment,
    • Those who have migraine, are in the postoperative period, have nerve damage, neuropathy and a vascular disease,
    • Those who have disabilities in grasping their hands,

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

96 participants in 3 patient groups

shotblocker
Experimental group
Description:
shotblocker
Treatment:
Other: shotblocker
palm stimulator
Experimental group
Description:
palm stimulator
Treatment:
Other: palm stimulator
control
No Intervention group
Description:
control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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