The effect of the nurse's speech on the pain and stress of neonates

The effect of the nurse's compassionate speech on the pain and stress of intravenous catheter insertion in premature neonates

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230529058335N1

Enrollment

Registered

2023-07-19

Start date

2023-07-23

Completion date

Unknown

Last updated

2023-07-25

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

Conditions

The study is about the pain and stress of premature neonats during intravenous catheter insersion.. Acute pain, not elsewhere classified

Interventions

Intervention 1: Intervention group: 6 nurses who meet the entry criteria are trained in compassionate talking with neonate.And one day, during a shift, they talk to their neonate for at least 45 minut

Eligibility

Sex/Gender

All

Age

112 Days to 136 Days

Inclusion criteria

Inclusion criteria: Entry requirements for neonates : Neonats weighing more than 1 kg Premature neonats with a gestational age of 28 to 34 weeks Since feeding the neonate at least one hour has passed The neonat should be calm and alert The neonats 's hearing is healthy with the OAE test The parents of the neonat must consent to participate in the research Entry requirements for nurses : Willingness to cooperate in this research At least 3 years of work experience in the neonatal intensive care unit

Exclusion criteria

Exclusion criteria: Conditions for non-entry of neonates : The Apgar score of the fifth minute of the neonat should be less than 6 have a major congenital anomaly The neonat need CPAP or connected to a tracheal tube have a history of taking analgesic and sedative medicine in the past 24 hours The neonat's mother should be addict Have a history of surgery Conditions for non-entry of nurses : Violence and tightness of the vocal cords

Design outcomes

Primary

Measure	Time frame
The amount of pain in neonates of the intervention and control groups will be evaluated. Timepoint: 1 minute before the start of the intervention, the first 30 seconds of the start of the intervention, 1 and 5 minutes after the end of the intervention. Method of measurement: Registering ?the amount of pain in neonates using the (PIPP) premature infant pain profile.;The amount of stress in neonates of the intervention and control groups will be evaluated. Timepoint: 1 minute before the start of the intervention, the first 30 seconds of the start of the intervention, 1 and 5 minutes after the end of the intervention. Method of measurement: Registering the amount of stress in neonates using the (NISS) newborn infant stress scale.	—

Measure

Time frame

The amount of pain in neonates of the intervention and control groups will be evaluated. Timepoint: 1 minute before the start of the intervention, the first 30 seconds of the start of the intervention, 1 and 5 minutes after the end of the intervention. Method of measurement: Registering ?the amount of pain in neonates using the (PIPP) premature infant pain profile.;The amount of stress in neonates of the intervention and control groups will be evaluated. Timepoint: 1 minute before the start of the intervention, the first 30 seconds of the start of the intervention, 1 and 5 minutes after the end of the intervention. Method of measurement: Registering the amount of stress in neonates using the (NISS) newborn infant stress scale.

—

Secondary

Measure	Time frame
Success rate in venous catheter placement. Timepoint: After each intervention. Method of measurement: The number of unsuccessful attempts to insert a venous catheter.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReyhaneh Omidvar

Mashhad University of Medical Sciences

omidvarR4012@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

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