Effectiveness of Vapocoolant Spray on Venipuncture Pain in Young Male Donors

Saglik Bilimleri Universitesi

Status: Completed

Conditions: Pain; Venipuncture

Treatments: Other: Vapocoolant spray

Study type: Interventional

Funder types: Other

Identifiers

NCT04346732

SAciksoz

Details and patient eligibility

About

Aim: The aim of this study is to assess the effectiveness of vapocoolant spray in reducing pain related to venipuncture in young, healthy male blood donors.

Hypotheses:

H1: Vapocoolant spray reduces venipuncture pain during blood donation. H0: Vapocoolant spray does not reduce venipuncture pain during blood donation.

Full description

After being informed about the study and potential risks, all patients giving written informed consent. Before the procedure was begun, the donors who agreed to participate in the study were met face-to-face and asked to fill in the "Informative Characteristics Form", the "VAS", the "Blood/Injection Fear Scale" and the "STAI-I" forms.Then the donors were assigned to their groups by the researcher.The donors in the control group were not given any intervention during the blood collection process. Vapocoolant spray was applied to the donors in the vapocoolant spray group. During the blood collection procedure, after the donors' skin was cleaned with antiseptic solution, spray was applied to the application site for a maximum of 10-15 seconds from a distance of 25 cm. In both groups, immediately following venipuncture, pain assessment was made with the VAS by the researcher, who did not know which group each participant belonged to.

Enrollment: 88 patients

Sex: Male

Ages: 18 to 35 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• aged between 18 and 35
• BMI between 18.5 and 24.9 kg/m2
• speaks turkish
• male donor
• individuals who applied to make voluntary blood donations
• volunteers to participate in the study

Exclusion criteria

• donors who did not agree to take part in the study,
• donors with open wound, scar, infection, dermatitis, eczema or lesion at the venipuncture site, or donors with cold allergy

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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88 participants in 2 patient groups

Vapocoolant spray

Experimental group

Description:

Vapocoolant spray was applied to the donors in the vapocoolant spray group.

Treatment:

Other: Vapocoolant spray

Control

No Intervention group

Description:

The donors in the control group were not given any intervention during the blood collection process.