Actively Recruiting

Age: 18Years +
All Genders
NCT07389330

Patients' Perceptions of Postoperative Analgesic Monitoring in Elective General Surgery

Led by Agri Ibrahim Cecen University · Updated on 2026-04-07

300

Participants Needed

1

Research Sites

10 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study examines how patients perceive postoperative analgesic monitoring during routine care in elective general surgery. Postoperative pain monitoring is a standard nursing practice, but patients may experience it as either supportive or stressful. These perceptions may influence patients' trust in nursing care, anxiety related to monitoring, and willingness to report pain accurately. The study uses a mixed-methods observational design. In the quantitative phase, patients complete questionnaires about their experiences with pain monitoring, communication with nurses, trust, anxiety, and pain reporting during the first days after surgery. In the qualitative phase, selected patients participate in interviews to further explain and contextualize the survey findings. No changes are made to standard care, and no experimental treatments are used.

CONDITIONS

Official Title

Patients' Perceptions of Postoperative Analgesic Monitoring in Elective General Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Undergoing elective general surgery requiring postoperative inpatient care
  • Receiving routine postoperative analgesic monitoring as part of standard clinical care
  • Clinically stable during the postoperative data collection period
  • Able to read and communicate in Turkish
  • Able and willing to provide written informed consent
Not Eligible

You will not qualify if you...

  • Emergency or urgent surgical procedures
  • Postoperative admission to an intensive care unit
  • Requirement for mechanical ventilation
  • Documented cognitive impairment, acute delirium, or severe psychiatric illness
  • Inability or unwillingness to complete study questionnaires or interviews

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ağrı Training and Research Hospital

AĞRI, Merkez, Turkey (Türkiye), 04100

Actively Recruiting

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Research Team

V

VOLKAN GOKMEN, Assistant Professor

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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