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The effect distraction on patients undergoing hemodialysis

Compare auditory distraction and visual distraction on pain, stress and vital sign changes from due to needles insertion into arteriovenous fistula in elderly patients undergoing hemodialysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201709047529N14
Enrollment
120
Registered
2017-09-19
Start date
2017-07-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Arteriovenous fistula puncture-related complication in hemodialysis patients. Mechanical complication of vascular dialysis catheter

Interventions

Intervention 1: Interventions 1: For the auditory distraction intervention group at three intermittent hemodialysis sessions, nature based sounds at three time films about nature will be done for 20 m
Interventions 1: For the auditory distraction intervention group at three intermittent hemodialysis sessions, nature based sounds at three time films about nature will be done for 20 minutes. Skin wi
For the visual distraction intervention group at three intermittent hemodialysis sessions, films about nature will be done for 20 minutes. Skin will be disinfected for vein puncture. Fistula is then
Skin will be disinfected for vein puncture. Fistula is then punctured. at three intermittent hemodialysis sessions, the intensity of stress before injection and the intensity pain after injection will

Sponsors

Shahed University Vice Chancellor For Research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 139 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: the desire to participate in the study; over 60 years old; hemodialysis patients who have at least three session of dialysis at week; patients who have at least three months past of their fistula embedding; without alcohol and drugs consumption; the absence of cognitive impairment; not having vision or hearing problems; no history of mental illness with doctor approval. Exclusion criteria: patient dissatisfaction to continue participation in the study; lack of turn later; candidate for a transplant; using analgesic or non-pharmacological to reduce pain in the past 24 hours; in need of a second needle insertion into arteriovenous fistula in case of failure in the first of the fistulas needles; pain existence in the other parts of body.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: After every intervention and immediately after the fistula needle. Method of measurement: Visual Pain Scale.;Quality of pain. Timepoint: After every intervention and immediately after the fistula needle. Method of measurement: short-form McGill pain questionnaire.;Blood pressure. Timepoint: After every intervention and immediately after the fistula needle. Method of measurement: Checklist.;Respiratory rate. Timepoint: After every intervention and immediately after the fistula needle. Method of measurement: Checklist.;Heart rate. Timepoint: After every intervention and immediately after the fistula needle. Method of measurement: Checklist.;Stress. Timepoint: After every intervention and before the fistula needle. Method of measurement: Stress visual analogue scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Nahid Rejeh

Shahed University

nrejeh@yahoo.com+98 21 5121 3071

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026