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Familiar auditory stimuli on physiological responses induced by painful stimulation in infants

Assessing of impact the auditory familiar stimulation on physiological responses caused by painful stimuli in newborns hospitalized in NICU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014011416225N1
Enrollment
60
Registered
2014-08-03
Start date
2014-06-22
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

Understand the relationship between auditory stimulation on physiological responses induced by painful stimulation in infants hospitalized in intensive care. Acute pain R52.0

Interventions

Intervention 1: In the test group, the mother's voice is played for 10 minutes before and 10 minutes after blood sampling continues. Mother's voice can be recorded using a software program, Cool Edit2
In the test group, the mother's voice is played for 10 minutes before and 10 minutes after blood sampling continues. Mother's voice can be recorded using a software program, Cool Edit2000,and with two

Sponsors

Baghiatollah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Infants hospitalized in neonatal intensive care units in selected hospitals in Tehran; when measuring pain or at least 3 hours before it, Sedatives have not received; The lack of Underlying disease and extensive surgery (e.g., abdominal surgery, etc.) that is causing pain; The lack of crippling diseases and anatomical defects members (hands and feet); No hearing impaired; Must have at least 36 weeks gestational age; Requiring Blood samples is. Exclusion criteria: During the study, the infant is in trouble, as it is connected to the ventilator; when sampling is not done once the needles into the skin; when sedatives or tranquilizers should be used for infants during Blood samples

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Physiological responses. Timepoint: Before the intervention, during intervention, post-intervention. Method of measurement: Using a pulse oximeter Mobile.

Secondary

MeasureTime frame
Pain. Timepoint: Before the intervention, during intervention, post-intervention. Method of measurement: NIPS pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Azarmnejad

Baghiatollah University of Medical Sciences

azarm.elham2yahoo.com+98 11 4254 2397

Outcome results

None listed

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