The Effectiveness of an Interventional-Supportive Program on Children's Anxiety and Pain

The Effectiveness of an Interventional-Supportive Program on Children's Anxiety and Pain Hospitalized in Surgery Department

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20191004044976N1

Enrollment

Registered

2020-04-19

Start date

2020-01-21

Completion date

Unknown

Last updated

2020-05-18

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

Conditions

Pediatric surgery ?.

Interventions

Intervention 1: Intervention group: One day after the surgery,first the child's pain is assessed by Toddler-Preschool-Post operative scale and the child's anxiety is assessed using self-report Piyeri

Eligibility

Sex/Gender

All

Age

3 Years to 6 Years

Inclusion criteria

Inclusion criteria: 3 to 6 year old children Having mental health and consciousness Surgery on the gastrointestinal Children whose hospitalization is longer than two days after surgery

Exclusion criteria

Exclusion criteria: Taking anti anxiety drugs Having growth and mental retardation Having a history of chronic illness (epilepsy, seizures, diabetes, diagnosed heart disease, kidney disease) Previous surgical experience Taking anti pain drugs

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Before intervention, One hour After intervention. Method of measurement: Toddler-Preschool-Post operative scale(TPPPS).;Anxiety. Timepoint: Before intervention, One hour After intervention. Method of measurement: Piyeri's Self-report tool for severity of anxiety.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSima Askari

Esfahan University of Medical Sciences

simaaskari@nm.mui.ac.ir+98 31 3627 7821

Outcome results

None listed

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