NCT07389330

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

87
On Track

Trial Health Score

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

Enrollment
312

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Feb 2026

Shorter than P25 for all trials

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 25, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

February 5, 2026

Completed
10 days until next milestone

Study Start

First participant enrolled

February 15, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 15, 2026

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2026

Completed
Last Updated

June 2, 2026

Status Verified

May 1, 2026

Enrollment Period

2 months

First QC Date

January 25, 2026

Last Update Submit

May 31, 2026

Conditions

Keywords

postoperative analgesic monitoringelective general surgerypain disclosuretrust in nursing carestructural equation modeling

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.

Other: No intervention (observational study)

Interventions

No intervention is applied in this study. Participants receive standard postoperative care, including routine analgesic monitoring, as part of usual clinical practice.

Elective General Surgery Patients

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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)

Location

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: 24237004BACKGROUND
  • Salmon 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: 9251999BACKGROUND
  • Ip 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: 19672167BACKGROUND
  • Qaddumi 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

Pain, PostoperativeAgnosia

Interventions

Observation

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and SymptomsPerceptual DisordersNeurobehavioral ManifestationsNervous System Diseases

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

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.

Locations