The effect of self-selected calming music on pain intensity due to needle insertion in to a fistula in hemodialysis patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201607297494N20

Enrollment

114

Registered

2016-08-08

Start date

2016-08-22

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

pain. pain, unspecified

Interventions

Intervention 1: Intervention of group 1: First in intervention group with music, pain degree due to needle insertion into an arteriovenous fistula will be recorded with visual measure immediately afte

Intervention of group 1: First in intervention group with music, pain degree due to needle insertion into an arteriovenous fistula will be recorded with visual measure immediately after needle inserti

Other interventions Intervention of group 2( headphone group): First in the intervention group with headphone during a session of hemodialysis, without any intervention, the pain degree due to needle

Control group: For control group based on ward’s routine, needle insertion in to a fistula will be done without any intervention. Then a minute after end of venopuncture and fixing needle, the pain de

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria: willing to listen to music; being 18 years or older; lack of neuropathic disorders; havingno known history of depression; being treated with hemodialysis for at least 3 months; not being administered analgesics and sedatives within 3 hours before needle insertion into a fistula; having no history of taking antipsychotic drugs; not being mentally impaired; having no visual and hearing dysfunction and not being habited to listen to music during hemodialysis. Exclusion criteria: existence the acute pain in other area of body; need to try for needle insertion in to a fistula more than once; change in physical condition; refusing to continue study and death.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: before and after intervention. Method of measurement: visual analoug scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Masoumeh Bagheri- Nesami

Mazandaran University of Medical Science

anna3043@gmail.com+98 11 3336 7551

Outcome results

None listed

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