NCT07830498

Brief Summary

This study examines whether surgical nurses' confidence in managing patients' pain (pain management self-efficacy) is related to how well their patients' pain is managed after surgery. Nurses working in general surgery clinics will complete a questionnaire about their own pain management self-efficacy, and the surgical patients under their care will complete a separate questionnaire about their postoperative pain outcomes. Each patient's responses will be linked to the nurse who cared for them, creating nurse-patient pairs, in order to explore how nurse-level factors relate to patient-level pain outcomes. This is an observational study: no treatment, medication, or intervention is provided or tested; participants only complete questionnaires.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
340

participants targeted

Target at P75+ for all trials

Timeline
2mo left

Started Oct 2026

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
not yet recruiting

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

Study Progress4%
Oct 2026Dec 2026

First Submitted

Initial submission to the registry

September 15, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 21, 2026

Completed
10 days until next milestone

Study Start

First participant enrolled

October 1, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

September 23, 2026

Status Verified

September 1, 2026

Enrollment Period

2 months

First QC Date

September 15, 2026

Last Update Submit

September 20, 2026

Conditions

Keywords

Pain ManagementSurgical NursingSelf-EfficacyNurse-Patient Dyad

Outcome Measures

Primary Outcomes (1)

  • Postoperative Pain Outcomes (Patients)

    Patient-reported postoperative pain outcomes measured with the Revised American Pain Society Patient Outcome Questionnaire (APS-POQ-R), including pain severity/intensity, pain interference with activity and sleep, and satisfaction with pain management. Each domain is rated on a 0-10 numeric rating scale; higher scores indicate worse outcomes for the pain severity/intensity and interference-with-activity/sleep domains, and higher scores indicate better outcomes (greater satisfaction) for the satisfaction-with-pain-management domain.

    Within 24-48 hours after surgery, prior to hospital discharge

Secondary Outcomes (1)

  • Nurses' Pain Management Self-Efficacy

    Measured once, at the time of study enrollment

Study Arms (2)

Surgical Nurses

Nurses working in and actively providing postoperative care in the participating general surgery clinics. Each nurse completed the Nurse Descriptive and Occupational Information Form and the Pain Management Self-Efficacy Questionnaire (PMSEQ, Turkish version) once. No intervention was applied.

Other: Pain Management Self-Efficacy and Postoperative Pain Outcome Assessment

Surgical Patients

Adult surgical patients receiving postoperative care in the participating general surgery clinics, each paired with the nurse primarily responsible for their care. Each patient completed the Patient Descriptive Information Form and the Revised American Pain Society Patient Outcome Questionnaire, Turkish version (APS-POQ-R-TR), within the first 24 postoperative hours. No intervention was applied.

Other: Pain Management Self-Efficacy and Postoperative Pain Outcome Assessment

Interventions

No therapeutic, experimental, or clinical intervention was administered; this is a purely observational, questionnaire-based study. Nurses' pain management self-efficacy was assessed once using the Pain Management Self-Efficacy Questionnaire (PMSEQ, Turkish version). Patients' postoperative pain outcomes were assessed once, within the first 24 postoperative hours, using the Revised American Pain Society Patient Outcome Questionnaire, Turkish version (APS-POQ-R-TR). Usual clinical care and pain management practices were not modified in any way.

Surgical NursesSurgical Patients

Eligibility Criteria

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

Surgical nurses providing postoperative care in the general surgery clinics of two training and research hospitals in Turkey, together with the adult surgical patients under their care during the first 24 postoperative hours, forming linked nurse-patient dyads.

You may qualify if:

  • Surgical Nurses:
  • Currently employed as a registered nurse
  • Working in the general surgery clinic where the study is conducted
  • Actively involved in postoperative patient care
  • Employed in the relevant clinic for at least 3 months
  • Voluntarily agrees to participate in the study
  • Surgical Patients:
  • years of age or older
  • Has undergone a surgical procedure
  • Receiving postoperative care in the general surgery clinic where the study is conducted
  • Within the first 24 postoperative hours
  • Able to communicate in Turkish
  • Conscious and cognitively able to answer study questions
  • Voluntarily agrees to participate in the study

You may not qualify if:

  • Surgical Nurses:
  • On extended leave or medical report during the data collection period, resulting in no active clinical care
  • Does not complete the data collection form during the study period
  • Surgical Patients:
  • Followed in the intensive care unit
  • Impaired consciousness that prevents assessment
  • Serious cognitive or communication impairment that prevents communication
  • Underwent emergency surgery
  • Unable to complete the study data collection forms

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Agri Training and Research Hospital, General Surgery Clinic

Ağrı, Turkey (Türkiye)

Location

Taksim Training and Research Hospital, General Surgery Clinic

Istanbul, Turkey (Türkiye)

Location

Related Publications (4)

  • Aydin Sayilan A, Eskin Bacaksiz F, Seyhan Ak E, Kulakac N, Macindo JRB. Adaptation of the pain management self-efficacy questionnaire into Turkish. Agri. 2022 Apr;34(2):91-99. doi: 10.14744/agri.2022.35902.

    PMID: 35848809BACKGROUND
  • Macindo JRB, Soriano CAF, Gonzales HRM, Simbulan PJT, Torres GCS, Que JC. Development and psychometric appraisal of the Pain Management Self-Efficacy Questionnaire. J Adv Nurs. 2018 Apr 6. doi: 10.1111/jan.13582. Online ahead of print.

    PMID: 29633327BACKGROUND
  • Erden S, Guler S, Tura I, Basibuyuk IF, Arslan UE. Evaluating patient outcomes in postoperative pain management according to the revised American Pain Society Patient Outcome Questionnaire (APS-POQ-R). Appl Nurs Res. 2023 Oct;73:151734. doi: 10.1016/j.apnr.2023.151734. Epub 2023 Aug 18.

    PMID: 37722782BACKGROUND
  • Erden S, Karadag M, Guler Demir S, Atasayar S, Opak Yucel B, Kalkan N, Erdogan Z, Ay A. Cross-cultural adaptation, validity, and reliability of the Turkish version of revised American Pain Society patient outcome questionnaire for surgical patients. Agri. 2018 Apr;30(2):39-50. doi: 10.5505/agri.2018.21548.

    PMID: 29738065BACKGROUND

MeSH Terms

Conditions

Pain, PostoperativeAgnosia

Condition Hierarchy (Ancestors)

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

Study Officials

  • Volkan Gokmen, PhD, RN

    Agri Ibrahim Cecen University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Volkan Gokmen, PhD, RN

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

September 15, 2026

First Posted

September 21, 2026

Study Start

October 1, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

September 23, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will not share

To protect participant confidentiality, individual-level nurse and patient data linked by coded identifiers will not be shared outside the research team.

Locations