Patients' Perceptions of Postoperative Analgesic Monitoring in Elective General Surgery
PSAM-SEM
1 other identifier
observational
312
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 25, 2026
CompletedFirst Posted
Study publicly available on registry
February 5, 2026
CompletedStudy Start
First participant enrolled
February 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedJune 2, 2026
May 1, 2026
2 months
January 25, 2026
May 31, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain Disclosure Behavior
Pain disclosure behavior is measured using the Pain Disclosure Behavior Scale (PDB), a self-report questionnaire consisting of 3 items. Each item is rated on a 5-point Likert scale ranging from 1 (strongly disagree) to 5 (strongly agree). Total scores range from 3 to 15, with higher scores indicating greater willingness to report pain accurately and to request analgesia when needed.
Postoperative days 1 to 3
Secondary Outcomes (5)
Trust in Nursing Care
Postoperative days 1 to 3
Monitoring-Related Anxiety
Postoperative days 1 to 3
Perceived Surveillance-Oriented Analgesic Monitoring
Postoperative days 1 to 3
Perceived Supportive Analgesic Monitoring
Postoperative days 1 to 3
Perceived Nursing Communication Quality
Postoperative days 1 to 3
Other Outcomes (1)
Patient Experiences of Postoperative Analgesic Monitoring
Up to 48 hours following surgery
Study Arms (1)
Elective General Surgery Patients
Adult patients undergoing elective general surgery who receive routine postoperative analgesic monitoring as part of standard clinical care.
Interventions
No intervention is applied in this study. Participants receive standard postoperative care, including routine analgesic monitoring, as part of usual clinical practice.
Eligibility Criteria
The study population consists of adult patients undergoing elective general surgery who are hospitalized postoperatively and receive routine analgesic monitoring as part of standard nursing care in a tertiary university hospital.
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ağrı Training and Research Hospital
AĞRI, Merkez, 04100, Turkey (Türkiye)
Related Publications (4)
Gan TJ, Habib AS, Miller TE, White W, Apfelbaum JL. Incidence, patient satisfaction, and perceptions of post-surgical pain: results from a US national survey. Curr Med Res Opin. 2014 Jan;30(1):149-60. doi: 10.1185/03007995.2013.860019. Epub 2013 Nov 15.
PMID: 24237004BACKGROUNDSalmon P, Manyande A. Good patients cope with their pain: postoperative analgesia and nurses' perceptions of their patients' pain. Pain. 1996 Nov;68(1):63-68. doi: 10.1016/S0304-3959(96)03171-5.
PMID: 9251999BACKGROUNDIp HY, Abrishami A, Peng PW, Wong J, Chung F. Predictors of postoperative pain and analgesic consumption: a qualitative systematic review. Anesthesiology. 2009 Sep;111(3):657-77. doi: 10.1097/ALN.0b013e3181aae87a.
PMID: 19672167BACKGROUNDQaddumi J, Arda AM, Alkhawaldeh A, ALBashtawy M, Abdalrahim A, ALBashtawy S, Al Omari O, Bashtawi M, Masa'deh R, ALBashtawy Z, Mohammad KI, ALBashtawy B, Aljezawi M, Khatatbeh H, Ta'an W, Suliman M, Al Dameery K, Bani Hani S. Preoperative anxiety, postoperative pain tolerance and analgesia consumption: A prospective cohort study. J Perioper Pract. 2025 Oct;35(10):426-436. doi: 10.1177/17504589241253489. Epub 2024 Aug 6.
PMID: 39104294BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
January 25, 2026
First Posted
February 5, 2026
Study Start
February 15, 2026
Primary Completion
April 15, 2026
Study Completion
April 30, 2026
Last Updated
June 2, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared. The study involves patient-reported perceptions, psychosocial measures, and qualitative interview data collected in a postoperative clinical setting. Sharing IPD could pose a risk to participant confidentiality and privacy. Only aggregated and anonymized results will be reported in publications.