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Effect of warm footbath on arteriovenous fistula puncture-related pain in hemodialysis patients

Effect of warm footbath with and without vibration on arteriovenous fistula puncture-related pain in hemodialysis patients at educational - medical hospitals of Qazvin.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013091114634N1
Enrollment
31
Registered
2013-12-09
Start date
2013-07-23
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 pain in hemodialysis patients. Mechanical complication of vascular dialysis catheter

Interventions

This research will be an experimental study of the clinical trial with pre-test - post-test method with one group. After learning how to use a pain ruler to Samples, pain assessment will be performed

Sponsors

Vice chancellor for research, Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
17 Years to 65 Years

Inclusion criteria

Inclusion criteria: Major inclusion criteria: having an arteriovenous fistula; absence of evidence of peripheral vascular disease; no wounds to both legs above the ankle area; there is no impairment of consciousness and knowledge of the time and place and person; the ability to communicate verbally and audio; having age between 17-65 years; the last three months of fistula placement; no history of diabetes; no history of sensory and neurological disorders; Lack of consistent use of the substance, drug or relieve method to be effective on pain of fistula Needles. Major exclusion criteria: No need to go on hemodialysis; patients travel long; kidney transplantation; lack of consent to continue to participate in the study; the patient dies; if the patient is reported any other pain at evaluation or intervention time and or used of the substance, drug or relieve method which be effective on pain of Fistula Needles, excluded from the dialysis session and the next session will be enrolled in the study again but if this process is repeated in several sessions the patient will be completely excluded.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: In every hemodialysis session. Method of measurement: By using a numerical pain intensity scale (pain ruler).;Footbath with vibration method. Timepoint: Six intermittent hemodialysis sessions. Method of measurement: Method mentions in the information form.;Footbath without vibration method. Timepoint: Six intermittent hemodialysis sessions. Method of measurement: Method mentions in the information form.;Age. Timepoint: First meeting of evaluation. Method of measurement: Based on year in the information form.;Sex. Timepoint: First meeting of evaluation. Method of measurement: Based on sex in the information form.;Hemodialysis times a week. Timepoint: First meeting of evaluation. Method of measurement: Times number mentions in the information form.;The duration of arteriovenous fistula. Timepoint: First meeting of evaluation. Method of measurement: Based on year and month in the information form.;Arteriovenous fistula site. Timepoint: First meeting of evaluation. Method of measurement: Site mentions in the information form.;History of previous AVF. Timepoint: First meeting of evaluation. Method of measurement: Yes or no mentions in the information form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Abbas Ali Madadi

Qazvin University of Medical Sciences

Zabbasalimadadi@qums.ac.ir+98 28 1333 8127

Outcome results

None listed

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