CClinicalTrials.gg
CompletedNCT06567171Updated Aug 22, 2024

How Well Ethiopian Parents Assess and Manage Their Children's Postoperative Pain: Descriptive Correlational Study

An observational study in Parent, Pain and Ethiopia, sponsored by Wachemo University. Completed at 1 site in Ethiopia. Open to participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2024-08-22.

Sponsored by Wachemo University · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
102
Ages
18 Years to 45 Years
Sex
All
01

Study summary

This study aims to evaluate the practice of mothers towards the evaluation and management of postoperative children's pain.According to this study, Parents displayed low to moderate levels of knowledge adequacy towards the use of pain relief methods in relation to their children's postoperative pain and pain management, which indicates the need to provide parents with more information regarding their children's postoperative pain management.

Read the detailed description

Introduction: Acute postoperative pain in children is common. Although mothers care for their children's pain in most cases, it has been noted that mothers have limited knowledge about pain assessment and management of children.

Objectives: This study aims to evaluate the practice of parents towards evaluating and managing postoperative children's pain.

Method: This descriptive correlational study was conducted among 102 parents with children aged between 2 and 12 undergoing elective surgical procedures. Parental use of pain relief strategies (PURPS) and parental postoperative pain management (PPPM) tools were used to collect data on the adequacy of knowledge of using different pain relief strategies and the skill of parental pain assessment, respectively. Investigators used Spearman's rank correlation coefficient to determine the relationships between pain scores given by parents and nurses. The statistical tests were performed at a 95% confidence interval and a 5% significance level.

02

Conditions studied

  • Parent
  • Pain
  • Ethiopia
  • Hospital

Browse trials for

Keywords

  • Parents
  • Pain
  • Assessment
  • Management
  • Ethiopia
  • Wachemo University
03

In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's enrollment of 102 is close to the median of 102 across 608 observational studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Wachemo University is the lead sponsor of 4 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Parents whose children are receiving elective surgical procedures and are between the ages of two and twelve were included in the study.

Inclusion criteria

  • Parents whose children are receiving elective surgical procedures
  • age between the ages of two and twelve in year
  • The legal parents' fluency in the local language in speaking, writing, and reading,
  • lack of a diagnosis of any visual, auditory, sensory, or other illness

Exclusion criteria

Exclusion Criteria:

Children with

  • ASA classifications III or IV,
  • significant developmental delays,
  • chronic illnesses
  • premature births,
  • underlying chronic pain conditions (e.g., diabetes)
  • a medical history of multiple painful experiences (e.g., malignancies)
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
102 participants (actual)
Patient registry
No

Interventions

  • ProcedureThis descriptive correlational study was conducted among 102 parents with children aged between 2 and 12 undergoing elective surgical procedures.

    This descriptive correlational study was conducted among 102 parents with children aged between 2 and 12 undergoing elective surgical procedures. Parental use of pain relief strategies (PURPS) and parental postoperative pain management (PPPM) tools were used to collect data on the adequacy of knowledge of the use of different pain relief strategies and the skill of parental pain assessment, respectively. We used Spearman's rank correlation coefficient was used to determine the relationships between pain score given by parents and nurses. The statistical tests were performed at a 95% confidence interval and a 5% significance level.

06

What researchers measure

Primary outcomes

  1. To evaluate the quality of parents management of children's pain in postoperative period using observational tools called PURPS (Parental use of pain relief strategy) and PPPM (Parental postoperative pain measure)

    An observational tool was used to measure the quality of parental pain management

    Time frame: Oct, 2023

07

Study locations

1 site
  • Mitiku Desalegn
    Hosa'ina, Snnpr 667, Ethiopia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 22, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06567171
Lead sponsor
Wachemo University
Responsible party
Sponsor
First posted
Aug 22, 2024
Start date
Aug 12, 2022
Primary completion
Aug 12, 2022
Completion
Oct 20, 2022
Last update
Aug 22, 2024

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion