Information on the Use of Anti-embolic Stockings in Patients Undergoing Vein Surgery
The Effect of Information on the Use of Anti-embolic Stockings on Discharge Readiness and Satisfaction With Nursing Care in Patients Undergoing Vein Surgery
1 other identifier
interventional
60
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
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
June 13, 2025
CompletedFirst Posted
Study publicly available on registry
July 1, 2025
CompletedStudy Start
First participant enrolled
August 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 15, 2026
ExpectedJuly 1, 2025
May 1, 2025
4 months
June 13, 2025
June 26, 2025
Conditions
Keywords
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
EXPERIMENTALInformation 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.
Usual care
NO INTERVENTIONControl 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.
Eligibility Criteria
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
- PRINCIPAL INVESTIGATOR
Ezgi Arslan, PhD
Aydin Adnan Menderes University
Central Study Contacts
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
- 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.
The data sets generated during and/or analyzed during the current study are available from the corresponding author or reasonable request.