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Recruiting NCT07485088

Video-based Intervention to Reduce Anxiety in Patients Undergoing Elective PCI

No phase Interventional Procedural Anxiety Coronary Artery Disease Percutaneous Coronary Intervention Patients

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Video intervention.
Who it may be relevant to
Registry conditions: Procedural Anxiety, Coronary Artery Disease, Percutaneous Coronary Intervention Patients. Basic parameters: from 21 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Singapore
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effect of a Nurse-led Video-based Educational Intervention on Anxiety Among Hospitalised Patients Undergoing Elective Percutaneous Coronary Intervention: a Non-randomised Controlled Study

Overview

This study aims to evaluate the effectiveness of a video-based educational intervention in reducing anxiety among hospitalised patients scheduled for elective percutaneous coronary intervention (PCI). Participants will be assigned to either a video intervention group or a control group without randomisation. The intervention group will receive a structured educational video related to the PCI procedure, while the control group will receive usual care. Anxiety levels will be measured using the State-Trait Anxiety Inventory at baseline and after the intervention to determine whether the video intervention reduces anxiety before the procedure.

Interventions

  • Behavioral Video intervention
    Participants will watch a structured educational video explaining PCI

Primary outcome measures

  • Anxiety level [Time frame: Baseline (before intervention) After intervention / before PCI procedure]

Eligibility criteria

Inclusion criteria

  • adults scheduled for elective percutaneous coronary intervention
  • voluntary participation
  • ability to understand english
  • age 21 and above

Exclusion criteria

  • patients participating in other studies
  • outpatient PCI, urgent or emergency PCI
  • medically unstable
  • cognitive impairment

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Singapore · 1 center
  • Tan Tock Seng Hospital — Singapore

Identifiers

NCT: NCT07485088 · Project VIRA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗