NCT07044739

Brief Summary

The aim of this study was to investigate the effect of information given to patients undergoing vein surgery regarding the use of anti-embolic stockings on their readiness for discharge and satisfaction with nursing care.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
1mo left

Started Aug 2025

Shorter than P25 for not_applicable

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 Progress87%
Aug 2025Jun 2026

First Submitted

Initial submission to the registry

June 13, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

July 1, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

August 15, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Expected
Last Updated

July 1, 2025

Status Verified

May 1, 2025

Enrollment Period

4 months

First QC Date

June 13, 2025

Last Update Submit

June 26, 2025

Conditions

Keywords

nursing carevascular surgerydischargepostoperative period

Outcome Measures

Primary Outcomes (2)

  • Readiness for Discharge

    Readiness for discharge will be assessed with the Discharge Readiness Scale. : The scale consists of 8 questions and 4 sub-dimensions as personal status, knowledge, coping, and expected support. The questions in the scale are assessed between '0=not ready' and '10=completely ready'. A total of 0-80 points can be obtained from the scale according to the answers given to the questions, and an increase in the score indicates that the level of readiness of the patients for discharge increases. In the scale dimension scores, a score of 7 and above is assessed as the patient is ready for discharge, and a score below 7 is assessed as not ready for discharge.

    Immediately after the intervention

  • Nursing care satisfaction

    Nursing care satisfaction will be assessed with the Nursing Care Satisfaction Scale. The 19 items in the scale are 5-point Likert type and aim to define patients' satisfaction with various aspects of nursing care. The scoring used to determine the degree of satisfaction includes the following statements: 1- Not at all satisfied, 2- Rarely satisfied, 3- Satisfied, 4- Very satisfied, 5- Completely satisfied. The scale has no cut-off point. The patient's satisfaction with nursing care is assessed with the scale as long as the patient stays in the patient's room. The score evaluation is made on a 0-100 score by adding the scores of all items on the scale and converting them to 100. It is reported that a total score of 100 indicates satisfaction with all aspects of nursing care. A high total score also indicates high patient satisfaction.

    Immediately after the intervention

Study Arms (2)

Training on the use of anti-embolic stockings

EXPERIMENTAL

Information will be provided on the use of anti-embolic stockings. During the information session, an educational material titled "Use of Anti-Embolic Stockings" will be prepared by the researcher for the patients. The content of the training will be created to cover the purpose of using anti-embolic stockings, how to use them, and the points to be considered during use. The training is expected to take approximately 20 minutes. The training will be given face-to-face in the patient room by the researcher. The created training material will be evaluated in terms of content and form by 1 specialist in the field of Cardiovascular Surgery and 4 specialists in the field of Surgical Diseases Nursing using the "Nursing Education Material Evaluation Tool" (HEMDA) and expert opinions will be obtained. The content of the training material will be finalized in line with the opinions received.

Behavioral: Patient Education on the Use of Anti-Embolic Stockings

Usual care

NO INTERVENTION

Control group patients will receive routine nursing care in the clinic.

Interventions

The researcher will provide verbal information to the patients with the educational material titled "Use of Anti-Embolic Stockings", the stages of wearing anti-embolic stockings will be shown to the patients, and the educational material will be left next to the patients in the intervention group. The educational content covers the purpose of using anti-embolic stockings, how to use them, and the points to be considered during use.

Training on the use of anti-embolic stockings

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Having had vein surgery

You may not qualify if:

  • Having hearing/vision/mental problems
  • Having been diagnosed with a psychological illness (schizophrenia, depression)
  • Having any of the contraindications for the use of anti-embolic stockings in the patient (the patient has peripheral arterial disease or bypass grafts, peripheral neuropathy or other causes of sensory impairment, heart failure, pulmonary or leg edema, poor skin condition due to dermatitis/diabetes/venous ulcers, allergy or sensitivity to the materials in the stockings, and leg deformities that prevent the stockings from fitting properly)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Ezgi Arslan, PhD

    Aydin Adnan Menderes University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Ezgi Arslan, PhD, Research Assisstant

CONTACT

Ezgi Arslan, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD, Research Assisstant (Principal Investigator)

Study Record Dates

First Submitted

June 13, 2025

First Posted

July 1, 2025

Study Start

August 15, 2025

Primary Completion

December 15, 2025

Study Completion (Estimated)

June 15, 2026

Last Updated

July 1, 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 or reasonable request.

Shared Documents
CSR
Time Frame
12 months after publication
Access Criteria
Relevance to the topic of the study and approval of all-authors within 1 month of receiving the request.