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NCT07700680Not yet recruiting

Effect of 4-7-8 Breathing on AV Fistula Needle Pain in Dialysis Patients

The Effect of a 4-7-8 Breathing Exercise Program on the Management of Arteriovenous Fistula Intervention Pain in Hemodialysis Patients: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 15 Jul 2026

Brief summary (registry, in English)

For many hemodialysis patients, needle insertion into the vascular access site (fistula) is a significant source of pain and anxiety. In this study, patients will be guided to perform breathing exercises using the 4-7-8 breathing technique during needle insertion to reduce this pain. A total of 80 adult patients undergoing regular hemodialysis at Izmir Atatürk Training and Research Hospital will be randomly assigned to two groups: an intervention group and a control group. Participants in the intervention group will be taught a standardized intervention program consisting solely of the 4-7-8 breathing technique, to be applied before and during AVF cannulation. The program will be implemented during every hemodialysis session (three times a week) for one week. The technique will be explained in person by a research nurse before the first session, and patients will be provided with a short instructional video demonstrating the technique step by step. The video will be sent to patients' smartphones to encourage them to practice at home. Participants in the control group, however, will continue with their current routine hemodialysis care and standard cannulation procedures (without any structured breathing exercises). The results of this study may provide nurses and patients with easy-to-use, evidence-based options to make hemodialysis needle procedures less painful and stressful.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
8 Jul 2026
Start date
20 Jul 2026
Primary completion date
25 Jul 2026
Lead sponsor
Izmir Kavram Vocational School
NCT number
NCT07700680

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 20 Jul 2026 to the primary completion date, 25 Jul 2026
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Having a psychological disorder
    • Having communication problems
    • Having cancer
    • Not wanting to participate in the study

Who the study is looking for

  • Being 18-85 years of age or older
    • Receiving HD treatment 3 days a week
    • Being able to read and write
    • Having no hearing impairment
    • Having Turkish as their native language
    • Having received HD treatment for at least 6 months
    • Having a VAS pain score \>3
    • Agreeing to listen to music

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.