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Completed

NCT Number: NCT05548010

Venous Thromboembolism (VTE) Knowledge

Venous thromboembolism (VTE) is common especially among post-operative patients, and its occurrence is associated with significant morbidity and mortality. VTE is highly preventable with prophylactic modalities ranging from conservative measures such as early mobilization, to mechanical prophylaxis such as intermittent pneumatic compression (ICP), to pharmacological prophylaxis such as peri-operative anticoagulation. Despite established guidelines from various professional societies, the practice of VTE prophylaxis varied greatly from institute to institute. Evidence suggests that there is a significant gap between the optimal thromboprophylaxis as suggested by experts and real-work practice. Many healthcare-providers (HCP) and patients at risk of VTE are either not aware of the risk of VTE or not confident to apply the necessary thromboprophylaxis. The knowledge level of VTE appears to play a key role in affecting the level of compliance to the optimal thromboprophylaxis. Considerable improvement in VTE prophylaxis utilization may result from the implementation of a multifaceted educational program. By improving patient's awareness on VTE prophylaxis, the incidence of DVT might be reduced. The knowledge level of patients can be improved by various means including educational video, administrative measures, or continue medical education program. However, no prospective study has been performed to assess the impact of an educational program on the VTE knowledge level among post-operative patients and their HCP, and if any improvement of their knowledge level can be translated to a better adherence to VTE prophylaxis guidelines. We therefore propose to conduct a prospective non-randomized controlled study to evaluate the effect of an education materials for the patients as well as their HCP on their knowledge level as well as the utilization and adherence of VTE prophylaxis in these patients by comparing two groups of patients and HCP.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The Chinese University of Hong Kong

Shatin, 999077, Hong Kong

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Capable of providing written informed consent and willing and able to adhere to all protocol requirements
  • Male or female at least 18 years of age at the time of providing written informed consent
  • Adult patients age >18 scheduled for surgical operations
  • Healthcare Providers directedly involve in patients care of these surgical patients.

Exclusion criteria

  • Unable to make their own informed consent
  • Unable to understand the study protocol
  • Visually or auditorily impaired.

Treatment and study plan

No intervention as this is an observational study

Other

No intervention

Primary outcomes

  1. Difference in VTE knowledge between 2 groups

    Time frame: 4 weeks

    Difference between the knowledge level in the subject group and HCP group after the administration of the educational materials as measured with questionnaire

  2. VTE prophylaxis prescription by healthcare providers

    Time frame: 4 weeks

    Difference in VTE prophylaxis prescribed by HCP after the administration of the educational materials assessed upon patient follow-up/ discharge as reflected by drug prescription sheet and discharge summary

  3. VTE prophylaxis adherence

    Time frame: 4 weeks

    VTE prophylaxis will be advised to subjects upon discharge. Difference in VTE prophylaxis adherence of subjects after the administration of the educational materials will be assessed verbally during follow-up consultation by investigators.

Secondary outcomes

  1. Difference in VTE knowledge level within the HCP group

    Time frame: 4 weeks

    difference in VTE knowledge level within the HCP group before and after the administration of the educational materials as measured with questionnaire.

  2. Difference in patient satisfaction

    Time frame: 4 weeks

    Difference in patient satisfaction scoring before and after the administration of the educational materials to the HCPs assessed during patient follow-up consultation by investigators

  3. Difference in the rate of venous thromboembolism (VTE)

    Time frame: 4 weeks

    Difference in rate of VTE in the HCP group before and after the administration of the educational materials.

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Registry information

Official study title

Evaluation of a Short Educational Materials in Improving the Knowledge Level of Venous Thromboembolism and the Compliance of Thromboprophylaxis in Post-operative Patients: a Prospective Study

Important dates

Study start
2022
Primary completion
2023
Study completion
2024
First posted
Sep 21, 2022
Registry last updated
Nov 27, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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