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The Effect of Education on severity of pain and anexity

Effect of pre-operative face-to-face education on pain and anxiety of children with upper or lower extremities trauma undergoing outpatient surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016020714930N4
Enrollment
84
Registered
2016-04-17
Start date
2015-08-23
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

Condition 1: pain. Condition 2: anexity. Acute pain Generalized anxiety disorder

Interventions

Intervention 1: wound care have been described for the patients in the intervening group in a simple language. Intervention 2: Control group: No training.
wound care have been described for the patients in the intervening group in a simple language.
Control group: No training

Sponsors

Vice Chancellor for research Dezful Medical Sciences University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: nclusion criteria:age between 6 and 12 years old, lack of any sign of bone fractures, dislocation, amputation, presence of a foreign body, nerve damage, fever as well as infection, not using cast or splint at trauma site, having full consciousness and being able to understand and follow instructions to complete pain and anxiety assessment scales, children being accompanied by their parents (either mother or father) on the day of admission, speaking Persian (both children and their parents being able to speak and read Persian), lack of using sedative or analgesic before the surgery, lack of developmental, physical or psychological problems, not having previous hospitalization, emergency department admission or surgery after 18 months of age, and lack of having a long-term illness and/or pain that requires special medical care. Children who their parents disagreed to continue the study were excluded

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: before,during and 1 hour after the end of surgery. Method of measurement: Faces Pain Scale–Revised (FPS-R).

Secondary

MeasureTime frame
Anexity. Timepoint: before,during and 1 hour after the end of surgery. Method of measurement: Modified-Yale Preoperative Anxiety Scale (M-YPAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Beigom Bigdeli Shamloo

Dezful Medicine Sciences University

m.bigdeli@sbmu.ac.ir+98 61 4242 3912

Outcome results

None listed

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