How Well Ethiopian Parents Assess and Manage Their Children's Postoperative Pain: Descriptive Correlational Study
NCT ID: NCT06567171
Last Updated: 2024-08-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
102 participants
OBSERVATIONAL
2022-08-12
2022-10-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Traditional Ethiopian Coffee Ceremony in a Rural Ethiopian Hospital to Increase Hospital-based Delivery Rates
NCT04232137
Aromatherapy Versus Acupressure: Impact on Postoperative Pain and Sleep Quality in Pediatric Abdominal Surgery Patients
NCT07157501
Prevalence of Birth Before Arrival and Associated Factors Among Postpartum Women in Southern Ethiopia
NCT06434974
Non-Pharmacological Methods for Reducing Pain During Vaccination in Infants
NCT06886412
THE EFFECT OF HAND AND BACK MASSAGE ON PAIN, SLEEP AND SELF-CARE IN WOMEN UNDERGOING HYSTERECTOMY
NCT06403566
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
This 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.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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)
18 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Wachemo University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Mitiku Desalegn
Hosa’ina, Snnpr, Ethiopia
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NEMMCSH-WCU
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.