NCT07359118

Brief Summary

Patient-controlled analgesia (PCA) is a widely used method for postoperative pain management that allows patients to self-administer analgesics according to their pain needs. The safe and effective use of PCA depends largely on the knowledge and awareness of healthcare professionals. Insufficient knowledge may lead to improper use of PCA devices and increase the risk of complications affecting patient safety. The aim of this study will be to evaluate healthcare professionals' knowledge and attitudes regarding patient-controlled analgesia and to assess the effect of a structured educational intervention on these outcomes. This interventional, pre-post comparative study will be conducted among healthcare professionals working in surgical clinics, operating rooms, and intensive care units at a tertiary care hospital. Participants will complete a structured questionnaire assessing demographic characteristics, PCA-related knowledge, and attitudes before receiving a standardized educational program on patient-controlled analgesia. The same questionnaire will be administered again one week after the education. Changes in knowledge and attitude scores before and after the educational intervention will be analyzed using appropriate statistical methods.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
242

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 14, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 22, 2026

Completed
1 day until next milestone

Study Start

First participant enrolled

January 23, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 23, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 23, 2026

Completed
Last Updated

March 4, 2026

Status Verified

February 1, 2026

Enrollment Period

1 month

First QC Date

January 14, 2026

Last Update Submit

March 3, 2026

Conditions

Keywords

Patient-Controlled AnalgesiaPostoperative PainHealthcare ProfessionalsEducationKnowledge and Attitudes

Outcome Measures

Primary Outcomes (1)

  • Change in Knowledge Score on Patient-Controlled Analgesia

    The primary outcome is the change in healthcare professionals' knowledge regarding patient-controlled analgesia, assessed using a structured questionnaire consisting of true/false items administered before and after the educational intervention.

    From baseline (pre-education) to 1 week after the educational intervention

Study Arms (2)

Pre-Education Assessment Group

OTHER

Healthcare professionals who complete the study questionnaire before receiving the standardized patient-controlled analgesia educational program.

Behavioral: Patient-Controlled Analgesia Educational Program

Post-Education Assessment Group

OTHER

Healthcare professionals who complete the study questionnaire approximately one week after receiving the standardized patient-controlled analgesia educational program.

Behavioral: Patient-Controlled Analgesia Educational Program

Interventions

A standardized educational program on patient-controlled analgesia delivered to healthcare professionals. The program includes theoretical and practical content covering PCA principles, safe device use, opioid pharmacology, potential complications, patient monitoring, and follow-up. The education is provided through structured sessions and aims to improve participants' knowledge and attitudes regarding PCA.

Post-Education Assessment GroupPre-Education Assessment Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Healthcare professionals (physicians, nurses, anesthesia technicians, and midwives) working in surgical wards, operating rooms, or intensive care units.
  • Aged 18 years or older.
  • Actively involved in perioperative patient care.
  • Willing to participate in the study and provide informed consent.

You may not qualify if:

  • Healthcare professionals who decline to participate.
  • Incomplete or missing questionnaire responses.
  • Healthcare professionals not working in the specified clinical units.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kütahya City Hospital

Kütahya, 43100, Turkey (Türkiye)

Location

Related Publications (3)

  • Song Z, Cai J, Zhou Y, Jiang Y, Huang S, Gu L, Tan J. Knowledge, Attitudes and Practices Among Anesthesia and Thoracic Surgery Medical Staff Toward Ai-PCA. J Multidiscip Healthc. 2024 Jul 10;17:3295-3304. doi: 10.2147/JMDH.S468539. eCollection 2024.

    PMID: 39006875BACKGROUND
  • Kang MR, Kwon YJ. Nurses' knowledge and attitudes toward patient-controlled analgesia for postoperative pain control in a tertiary hospital in South Korea. BMC Nurs. 2022 Nov 22;21(1):319. doi: 10.1186/s12912-022-01106-7.

    PMID: 36419116BACKGROUND
  • Chen YR, Chen CC, Wu WW, Tang FI, Lu LC. Nurses' knowledge of and attitude toward postoperative patient-controlled analgesia (PCA) and the associated factors. BMC Nurs. 2024 Jan 5;23(1):21. doi: 10.1186/s12912-024-01702-9.

    PMID: 38183011BACKGROUND

MeSH Terms

Conditions

Pain, PostoperativeBehavior

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: This study uses a non-randomized, parallel-group design. Healthcare professionals assessed before the educational intervention and those assessed after the intervention may not be the same individuals. The pre-education and post-education groups are therefore treated as independent groups, and comparisons are made between these two parallel groups to evaluate the effect of the educational intervention.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 14, 2026

First Posted

January 22, 2026

Study Start

January 23, 2026

Primary Completion

February 23, 2026

Study Completion

February 23, 2026

Last Updated

March 4, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will not share

Locations