NCT06983288

Brief Summary

Since surgical patients are at risk of privacy violations in the perioperative process, it is thought that determining privacy perceptions and factors affecting this situation and developing strategies to protect privacy will improve the quality of patient care. In this study, it was aimed to determine the privacy perceptions of surgical patients in the perioperative process and the factors affecting them.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
294

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2024

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

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 15, 2024

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

May 14, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 14, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 14, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

May 21, 2025

Completed
Last Updated

May 28, 2025

Status Verified

May 1, 2025

Enrollment Period

7 months

First QC Date

May 14, 2025

Last Update Submit

May 22, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Privacy perceptions level

    Assessed with Perioperative Privacy Scale. The scale used to evaluate patient perceptions about privacy along perioperative period. It consisted 19 items with scoring from 1 (one) to 5 (five). The maximum score that can be obtained from the scale is 80 and the minimum score is 16. The scale score is high in patients whose privacy is protected and low in patients whose privacy is not protected. The high scores that can be obtained from the scale indicate that the privacy of the patients is protected.

    Time frame: Postoperative 1st day

Secondary Outcomes (1)

  • Comfort level

    Time frame: Postoperative 1st day

Eligibility Criteria

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

Undergoing urology, orthopaedics, general surgery and gynaecology operations

You may qualify if:

  • Being over 18 years old
  • Knowing and speaking Turkish
  • No communication problems
  • To have been operated in Aydın Adnan Menderes University Application and Research Hospital Hospital urology, orthopedics, general surgery and gynaecology service
  • At least 24 hours since the operation
  • To agree to participate in the research

You may not qualify if:

  • Hospitalisation in the intensive care unit

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Aydın Adnan Menderes University

Aydin, Zafer Mahallesi, 09010, Turkey (Türkiye)

Location

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Target Duration
1 Day
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD, Research Assisstant (Principal Investigator)

Study Record Dates

First Submitted

May 14, 2025

First Posted

May 21, 2025

Study Start

October 15, 2024

Primary Completion

May 14, 2025

Study Completion

May 14, 2025

Last Updated

May 28, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will share

The data sets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

Shared Documents
STUDY PROTOCOL
Time Frame
12 months after publication

Locations